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Radiotherapy Technologist - Radiology

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR

Apollo Hospitals Enterprise Limited

Pathology Lab Technician

Claims Adjudication - Associate Claims - BF - 38595-62366-3 - JR167225Position Title:Claims Adjudication - Associate Claims - BF - 38595-62366-3 - JR167225Job Family:CLM &gt; Claims SupportShift:Job Description:Job TitleAssociate ClaimsRequirement TypeFull-Time EmployeeJob LocationBangaloreRequirement LevelAssociateHiring ManagerTeam LeadPrimary SkillBusiness OperationsClaimsBusinessBusiness OperationsSkill CategoryGenericABOUT ELEVANCE HEALTH<a href="https://www.elevancehealth.com/" rel="noopener noreferrer" target="_blank">Elevance Health</a> is a leading health company in America dedicated to improving lives and communities and making healthcare simpler.  It is the largest managed health care company in the Blue Cross Blue Shield (BCBS) Association serving more than 46 million lives across 14 states. A regular in the <a href="https://fortune.com/ranking/fortune500/" rel="noopener noreferrer" target="_blank">Fortune 500</a> list, Elevance ranked 20 in 2025. <a href="https://fortune.com/ranking/most-powerful-women/" rel="noopener noreferrer" target="_blank">Gail Boudreaux</a>, President and CEO of Elevance has been a consistent name in the Fortune list of most powerful women and currently holds 53rd rank on this list. ABOUT CARELON<a href="https://www.linkedin.com/company/carelon-global-solutions/" rel="noopener noreferrer" target="_blank">Carelon Global Solutions</a> (CGS) is a healthcare solutions company that is simplifying complex operational processes to improve the health of the healthcare system. Previously known as Legato Health Technologies, Carelon Global Solutions (hereinafter, CGS) underwent a name change and joined the Carelon family of brands in January 2023, as a fully owned subsidiary of Elevance Health (Previously Anthem Inc.). CGS brings together a global team of like-minded innovators who manage and optimize operational processes for health plans as well as providers.Our brightest minds housed across our global headquarters in Indianapolis as well as Bengaluru, Hyderabad and Gurugram in India, Manila in the Philippines, Limerick in Ireland and San Juan in Puerto Rico bring with them innovative capabilities and an unmatched depth of experience. This global team uniquely positions CGS to enable scalable, next-generation platforms and specialized digital tools that make healthcare operations more practical, effective, and efficient.OUR MISSION &amp; VALUESOur Mission: Improving Lives and Communities. Simplifying Healthcare. Expecting More. Our Values: Leadership | Community | Integrity | Agility | DiversityJOB POSITIONCarelon Global Solutions India is seeking a highly creative and meticulous Associate - Claims, who will be responsible for all Processing level delivery &amp; performance as per set SLA parameters.  The incumbent will report to Team Lead – Business operations and must understand the business delivery, present and metrics with leadership; brief and deliver all in-house process delivery &amp; requirements, apart from coordinating with onshore partners as and when required.JOB RESPONSIBILITYAssociate – Claims(Business Operations) will be responsible for the following:<ul><li>Familiar with MS Office – basics (Excel/Power point/Outlook – primarily)</li><li>Very strong Communication &amp; Comprehension skills with the ability to evaluate key technical/Calculations needed to deliver basic process delivery</li><li>Working knowledge on basic technologies around persistence, search, graph and distributed technologies</li><li>Excellent oral and written communication skills</li><li>Healthcare domain knowledge - nice to have</li><li>Flexible to work in any shift &amp; in office premises per set organizational/Business requirements</li></ul>QUALIFICATION<ul><li>Bachelors’ or Masters’ degree</li><li>Non-BTech (preferably)</li></ul>EXPERIENCE<ul><li>0-2 years of overall experience including extra-ordinary internal personal skills, communication skills</li><li>Healthcare / Claims Experience will be added advantage</li></ul>SKILLS AND COMPETENCIES<ul><li>Responsible for Internal/Onshore calibration; Maintain updates tracker; Upskilling requirements &amp; plan upskilling sessions – as needed</li><li>Manage new hire associates and plan for their training and nesting as needed</li><li>Excellent Data management – Inventory allocated; status of pended / on hold inventory</li><li>Should be able to manage and track onshore connects, suggest/drive automation ideas &amp; demos and help them develop  as needed</li><li>Conduct team huddle on process updates, internal sample audit, participate in error review/root cause at operations level and provide performance data for group  aligned with</li><li>Agile &amp; Solution centric</li><li>Inclusive</li><li>Flexible to work in any shifts/Work from office</li></ul>THE CARELON PROMISEAligning with our brand belief of ‘limitless minds are our biggest asset’, we offer a world of limitless opportunities to our associates.It is our strong belief that one is committed to a role when it is not just what the role entails, but also what lies in its periphery that completes the value circle for an associate.This world of limitless opportunities thrives in an environment that fosters growth and well-being, and gives you purpose and the feeling of belonging.LIFE @ CARELON<ul><li>Extensive focus on learning and development</li><li>An inspiring culture built on innovation, creativity, and freedom</li><li>Holistic well-being</li><li>Comprehensive range of rewards and recognitions</li><li>Competitive health and medical insurance coverage</li><li>Best-in-class amenities and workspaces</li><li>Policies designed with associates at the center</li></ul>EQUAL OPPORTUNITY EMPLOYERCarelon is committed to a diverse and inclusive workplace and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity or expression, sexual orientation, national origin, genetics, pregnancy, disability, age, veteran status, or other characteristics.Reasonable AccommodationOur inclusive culture empowers Carelon to deliver the best results for our customers. We not only celebrate the diversity of our workforce, but we also celebrate the diverse ways we work.If you have a disability and need accommodation such as an interpreter or a different interview format, please ask for the Reasonable Accommodation Request Form.Disclaimer: Offered designation titles differ*Job Type:Full time<h4>Experience Level</h4>Entry Level

Carelon Global Solutions

Claims Assistant

Deputy General Manager - Program Management

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR<h4>Experience Level</h4>Mid Level

Project Head

EpidemiologistClarivate is a global leader in providing solutions to accelerate the lifecycle of innovation. Our bold mission is to help customers solve some of the world's most complex problems by providing actionable information and insights that reduce the time from new ideas to life-changing inventions in the areas of science and intellectual property. We help customers discover, protect, and commercialize their inventions using our trusted subscription and technology-based solutions coupled with deep domain expertise. We now have more than 11,500 colleagues in over 40 countries worldwide, and we work with over 200 partners to deliver value and success for our customers. Clarivate is a publicly traded company, listed on the New York Stock Exchange under the ticker NYSE:CLVT. As an Epidemiologist, you are responsible for conducting analytical research to support the needs of customers including performing fully documented systematic reviews of both published and grey literature on the epidemiology of assigned diseases and their risk factors to estimate incidence/prevalence over a 10–20-year period. Conduct research using online grey literature datasets such as NHANES, HCUP, cancer registries, government survey data, and other resources to summarize current information on prevalence, and to forecast numbers for a variety of diseases; and suggest use of proxy data sources or develop imputation or extrapolation models when country-specific sources are not available. You will also support other programs and units within the Company, for instance, by helping to maintain and enhance a sources database and by contributing to new products and proprietary consulting projects globally.About You – Experience, Education, Skills, and Accomplishments  •          Master’s degree in Epidemiology or Public Health•         Atleast 3 years of Systematic literature review experience•          A strong methodological background in epidemiology•          Familiar with MS Office including MS Word, Power Point, and Excel.It would be great if you also have…•          Experience with client interaction•          Experience analyzing large data sets•          Claims data analysis experience in SQL and/or Python•          Oncology experience•          RWD and SAS experienceAbout the TeamWe are a global team approximately 40+ team members located across U.S. Canada and India, specialized in Epidemiology.Work hoursMonday to Friday (Hybrid work model) 12PM – 9 PMAt Clarivate, we are committed to providing equal employment opportunities for all  qualified persons with respect to hiring, compensation, promotion, training, and other terms, conditions, and privileges of employment. We comply with applicable laws and regulations governing non-discrimination in all locations.<h4>Experience Level</h4>Mid Level

Clarivate

Health Informatics Specialist

Sr Investigator Payments AsstJob Summary The role is responsible for managing the complete lifecycle of investigator and site payments within clinical trials. This includes accurate payment calculations, timely processing, purchase order creation, and ensuring compliance with contractual and regulatory requirements. Key Responsibilities •    Provide exceptional service by resolving payment-related queries promptly, ensuring high satisfaction among external partners. •    Share expertise and facilitate knowledge transfer on all aspects of payment operations with business partners. •    Escalate issues appropriately and in a timely manner based on business impact. •    Support global, regional, and country-level initiatives to improve payment processes and drive operational efficiencies. •    Ensure payment requests are submitted accurately and on schedule, as per the Clinical Trial Agreement. •    Monitor and align payment metrics with established performance goals. •    Conduct interim and final payment reconciliations to maintain financial accuracy. •    Own and execute end-to-end payment coordination for assigned clinical studies. •    Maintain audit readiness and ensure compliance with applicable regulations and standards. •    Manage communication tools effectively, including email distribution, responsiveness, escalation handling, and prioritization.Qualifications •    Bachelor’s degree in any discipline. •    Language Proficiency: o    Mandatory: Fluency in one of the following languages — Chinese, Japanese, or Korean. o    Mandatory: Excellent verbal and written communication skills in English. •    1–3 years of professional experience; prior exposure to the pharmaceutical or clinical research industry is preferred. •    Familiarity with clinical payment processing, contracts, finance, and budgeting systems is a plus. •    Strong ability to collaborate across cross-functional teams and organizational levels. •    Excellent analytical thinking and problem-solving capabilities. •    Proficient in Microsoft Office Suite and general PC applications. •    Self-motivated with the ability to work independently. •    Experience working in a virtual or remote environment.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" rel="noopener noreferrer" target="_blank">https://jobs.iqvia.com</a><h4>Experience Level</h4>Senior Level

IQVIA

Billing Specialist

Associate Director, Patient Safety Technical SolutionsJob Title: Associate Director, Patient Safety Technical SolutionsGlobal Career Level: E<h4>Introduction to role</h4>The Patient Safety Technical Solutions Team as a part of the wider Patient Safety Operations, Technology and Analytics Team (OTA) is accountable for managing the information assets and systems owned by the Chief Medical Office (CMO), ensuring they are effectively supported and governed across the enterprise.Reporting to the ‘Director; PS Technical Solutions’, the ‘Associate Director; Patient Safety Technical Solutions’ provides Pharmacovigilance (PV) subject matter and technical expertise across AstraZeneca’s enterprise business-critical PV systems. The role holder works within a team of peers, all of whom employ an in-depth knowledge of business requirements, PV and regulatory policies, industry standards and trends as well as an understanding of the related assets to support effective governance, maintenance and development of the enterprise-wide systems that enable PV compliance and reporting.  The role holder will work within the Patient Safety Technical Solutions Team and will directly support the design, development, implementation, continuous improvement, and/or optimal utilization of AZ safety systems and assets.  He / She will understand how current and future components of the information and systems portfolio can be developed to ensure optimal benefit for the user community and the organization.The role has specific responsibility for informing and supporting the technical evolution of the PV systems estate throughout its lifecycle, ensuring it addresses changing external requirements and business goals (i.e. regulatory obligations, technological advancements, core business processes and information standards).  The role holder will also lead the capture and development of user requirements and protect AZ’s License to Operate (LtO) by ensuring that all change is conducted in line with applicable standards (e.g. GxP requirements, systems validation, privacy and security, etc). <h4>Accountabilities</h4><ul><li>Serves as a Subject Matter Expert (SME) within the Patient Safety Technical Solutions Team, ensuring it is capable of delivering high quality expertise and services across the PV systems estate, ensuring prioritized requirements and the strategic goals of stakeholders are understood and supported.</li><li>Manages applicable tools, documentation and methodologies to ensure processes and systems fully address the needs of organization.</li><li>Responsible for maintaining and evolving PV technology inclusive of relevant system processes, ensuring that the: <ul><li>Technology is changed in an effective and timely manner to meet new health authority requirements and / or changed business demands (e.g. divestment, in-licensing, partnership etc.). </li><li>Technical components of the system are upgraded in a compliant and risk-minimized manner.</li><li>Lead and coordinate routine system maintenance activities (e.g. MedDRA, WHODD, Ontology updates)</li><li>System enhancement requests are identified and prioritized (change control and major change projects). </li><li>Access to data is controlled, training requirements are defined and use of the system is compliant with all applicable regulations. </li><li>User support arrangements (e.g. training, helpdesk) and Service Level Agreements are in place, irrespective of whether delivered internally or by external vendors / providers.  </li></ul></li><li>Supports the ongoing business utilization of PS technology, including troubleshooting problems and developing solutions.  </li><li>Provides technical input and guidance on the development of strategic plans for PS technology across the enterprise. </li><li>Evaluates new modules and software upgrades and assesses the impact on system validation, the user community and PV processes.</li><li>Retains a global perspective around the business need for accurate, high-quality, effective and efficient information, while maintaining a focus on regulatory and corporate compliance needs.</li><li>Anticipates business, regulatory and wider industry trends, and apply these in the evolution and development of safety solutions.   </li><li>Accountable for ensuring the quality of business-related content of relevant improvement project proposals and associated documentation in line with Company goveranance process requirements.</li><li>Contributes to the development of procedures, work instructions, system specifications related to the use of Patient Safety Technical Solutions owned information sources and toolsets. </li></ul><h4>Essential Skills/Experience</h4><ul><li>Bachelor’s degree in a scientific discipline.</li><li>10+ years of relevant experience.</li><li>Proven competence, with extensive involvement in the successful design, delivery, validation, deployment or maintenance of information/systems solutions in support of safety.</li><li>Ability to articulate complex safety-related business needs in the context of IS systems design, architecture and development.</li><li>Experience in working across different geographic locations, organizations, and cultures.</li><li>Excellent interpersonal and communication skills with ability to efficiently communicate with all levels of the organization.</li><li>Strong knowledge on the below Technologies – Python, Oracle Apex, Power BI, Power Automate, SharePoint Online. </li></ul><h4>Desirable Skills/Experience</h4><ul><li>Higher degree in a clinical or safety-related discipline.</li><li>Significant experience in pharmacovigilance with proven record of supporting safety tools / solutions.</li><li>Broad knowledge of the safety information tools required to support drug development and marketed brands within AstraZeneca, including a comprehensive understanding of clinical trials, regulatory safety obligations, pharmacovigilance practices, epidemiology practices, and changing safety project team activities.</li><li>Awareness of broader technological developments both internally and externally leveraged to inform the design and development of AZ PV Systems.</li><li>Able to identify opportunities to lead change through continuous improvement based on strong awareness of external competitive practice.</li><li>Ability to lead diverse teams across multiple geographies to deliver on objectives (Leadership Capabilities).</li><li>Experience across multiple therapeutic or business areas, or in working in safety-related roles within other biopharmaceutical, regulatory, or health organizations.</li><li>Knowledge of the procedures, processes and standards governing clinical trial data (documents and data) with health authorities worldwide, and experience of implementing these within the business.</li></ul>Key Relationships to reach solutions Internal (to AZ or team)<ul><li>Head of GPS</li><li>PS Therapeudic Area (TA) partners</li><li>Information Technology partners</li><li>Data Science Teams</li><li>Other key science unit stakeholders across the enterprise</li></ul>External (to AZ)<ul><li>External regulatory authorities and industry/authority groups</li><li>Licensing Partners</li><li>External consultancy and/or staffing agencies</li><li>IS/IT partners and vendors</li></ul>When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.At AstraZeneca, we are driven by a shared vision to transform the way cancer is treated. Our commitment to science and innovation is unwavering, as we strive to make a meaningful impact on patients' lives. With one of the broadest Oncology pipelines in the industry, we offer unparalleled opportunities for growth and collaboration. Our supportive and diverse teams empower each other to take smart risks, challenge norms, and learn from every experience. Together, we are resilient and optimistic, working towards a future where cancer is no longer a cause of death.Ready to join us on this exciting journey? Apply now and be part of a team that's making a difference!Date Posted08-Oct-2025Closing Date19-Oct-2025AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.<h4>Experience Level</h4>Mid Level

Astrazeneca India Private Limited

Nurse Unit Manager

Customer-Market Access-ManagerAt EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all.     Job Summary:  Experience: 8+ years (Manager)  Life sciences – EU Market access We are seeking a highly experienced and strategic LS commercial and EU market access professional to join our life sciences team, to support blue chip pharmaceutical and biotech clients. The ideal candidate will bring over 8 years of experience in life sciences strategy consulting, with a strong foundation in commercial strategy, market access, and qualitative market research with HCPs and ex-payers. A key requirement for this role is extensive experience in leading projects like moderation of boards, mock negotiation workshops and payer strategy projects. The candidate should be adept at translating research findings into actionable insights and strategic recommendations.  Roles and Responsibilities: <ul><li>Lead and manage multiple market access projects across diverse therapy areas (significant oncology experience will be preferable)</li><li>Drive secondary research to build foundational knowledge for primary market research and strategic analysis.</li><li>Review and refine materials for primary market research including screeners, discussion guides, stimulus, discussion guide, pre-read material.</li><li>Lead qualitative interviews with HCPs, KOLs, and ex-payers to extract actionable insights.</li><li>Lead the analysis of the outputs from the interviews to tease out key insights, identify trends, and generate solutions to answer the research problem.</li><li>Prepare and lead client calls, workshops, and presentations to communicate findings and recommendations.</li><li>Develop and present high-impact client deliverables including strategic decks, and executive summaries.</li><li>Mentor and guide junior team members, fostering skill development and quality delivery.</li><li>Promote a culture of excellence, collaboration, and continuous learning within the team.</li><li>Leverage findings to develop an impactful client presentation deck and final reports to answer key client questions and develop strategic outputs.</li><li>Participate and co-moderate in and moderate workshops (virtual and in-person), such as ad-boards, evidence generation workshops, and other such workshops.</li></ul>  Key Competencies: <ul><li>Strong business analysis skills with experience in life sciences strategy, commercial strategy consulting, and market access.</li><li>Deep understanding of market access in Europe and the UK including HTA rules, IRP, the impact of EU-HTA regulations and other such topics that has an impact on the access and pricing of existing and upcoming therapies</li><li>Excellent communication and storytelling abilities to present data and insights to senior stakeholders and clients in a clear and compelling manner.</li><li>Ability to manage multiple priorities independently and deliver high-quality outputs under tight deadlines.</li></ul>  Desired Skills and Experience: <ul><li>Extensive experience in market access-related projects such as payer strategy, pricing research, evidence generation planning, mock negotiation workshops, advisory boards, and value story development</li><li>Drive proposal development and provide directions to team members on the methodology to be proposed, background section and other key information to be included</li><li>Drive development of thought leadership articles, ISPOR publications on key topics in the market access space</li></ul>  Minimum Qualifications: <ul><li>Bachelor's/ Master's degree in life sciences-related fields such as pharmaceutics, pharmaceutical chemistry, pharmacology, biotechnology from top-tier institutes</li><li>An MBA (in Pharma/healthcare/general) is preferred but not mandatory.</li></ul>  Other requirements: <ul><li>Relevant analytical experience in life sciences commercial strategy consulting.</li><li>Experience working across a broad range of projects in therapy areas like oncology, immunology and rare diseases</li><li>Strong verbal and written communication skills.</li><li>Proactiveness and passion for tackling new challenges.</li><li>Personal drive and positive work ethic to deliver results in demanding situations.</li></ul>  EY | Building a better working world    EY exists to build a better working world, helping to create long-term value for clients, people and society and build trust in the capital markets.     Enabled by data and technology, diverse EY teams in over 150 countries provide trust through assurance and help clients grow, transform and operate.     Working across assurance, consulting, law, strategy, tax and transactions, EY teams ask better questions to find new answers for the complex issues facing our world today.  <h4>Experience Level</h4>Mid Level

Ernst & Young LLP ( EY India )

Channel Marketing Executive

Associate-REMSJob Title: Associate- REMSGlobal Career Level: C2Shift Timings- 2:00-11:00pm ISTIntroduction to roleAre you ready to make a significant impact in the world of data analytics? As an Associate- REMS, you'll play a pivotal role in supporting Business Operations and driving data-driven decision-making within the Alexion ecosystem. Your expertise will enhance the quality and operational management of Commercial Risk Evaluation and Mitigation Strategies (REMS) data, ensuring accuracy and integrity across all REMS-related datasets. Dive into comprehensive data analytics and reporting, perform data quality checks, and provide essential insights to drive strategic initiatives and operational excellence. Are you up for the challenge?AccountabilitiesAs the Associate, you'll independently manage data quality review activities, monitoring data and reports for seamless integration and alignment across MDM, SAP, CRM, and downstream systems. You'll resolve synchronization issues while collaborating effectively across all commercial functions. Your responsibilities include maintaining high data quality and compliance for commercial REMS operations, supporting end-to-end REMS master data operations, ensuring continuous availability of vendor REMS data feeds, and contributing to REMS-related master data governance initiatives. Your strong communication skills will be key in delivering timely results and ensuring compliance.Essential Skills/ExperienceEducation • Bachelor's or Master's degree in Computer Science, Information/Data Sciences, Business, Technology, Engineering, or Mathematics. An advanced degree is a plus.Experience • 3+ years of data analytics experience. • Experience implementing and maintaining Master Data Management (MDM) systems, with strong knowledge of master data and REMS-related datasets. • Experience working within or with Commercial teams in the pharmaceutical or biotech sectors is preferred.Technical Skills • Proficiency with Veeva applications (including Network and Open Data) and Order Management Systems (particularly SAP). • Strong understanding of REMS data and requirements. • Proficiency in data management and analytical tools such as SQL and Python. • Expertise in managing and analyzing large, secondary transactional databases. • Familiarity navigating cloud-based data platforms (e.g., Snowflake). • Required MS Office skills, especially Excel and PowerPoint.Core Competencies &amp; Soft Skills • Data-Driven Mindset: Ability to understand, enrich, and make key master data elements available for business use. • Analytical &amp; Problem-Solving: Strong skills in deriving insights from complex datasets, managing multiple requests simultaneously, and quickly grasping new concepts. • Process-Oriented: Understands systems, processes, and workflows to generate and maintain high-quality data. • Collaboration: Proven track record of effective functional and cross-functional teamwork. • Communication: Excellent verbal and written communication skills for business interactions. • Organization &amp; Time Management: Strong organizational skills to manage tasks efficiently. • Self-Starter: Detail-oriented, able to work both independently and in a team environment. • Adaptability: Ability to thrive in a fast-paced, dynamic environment and eagerness to learn/implement new tools and capabilities.Bonus Points • Basic knowledge of Alexion brands. • Experience with data visualization tools like Power BI.When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.At AstraZeneca's Alexion division, you'll find an environment where innovation thrives! Our commitment to rare diseases means your work will have a profound impact on patients' lives. With a rapidly expanding portfolio, you'll enjoy the entrepreneurial spirit of a leading biotech while being supported by exceptional leaders and peers. Our culture celebrates diversity, inclusiveness, and integrity, fostering connections that drive meaningful change. Here, your career is not just a path but a journey towards making a difference where it truly counts.Ready to embark on this exciting journey? Apply now to join our team!Date Posted25-Sept-2025Closing Date05-Oct-2025Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact <a href="mailto:accommodations@Alexion.com" rel="noopener noreferrer" target="_blank">accommodations@Alexion.com</a>. Alexion participates in E-Verify.

Associate

Customer Relations Coordinator - Patient Care Services

 Dear Candidate,


 We are delighted to introduce you to Apollo Hospitals, a leading healthcare provider in India. With a long-standing heritage spanning many decades, Apollo Hospitals has established itself as a trusted name in the healthcare field, consistently delivering exceptional care with compassion.


 Renowned for our state-of-the-art medical facilities, advanced technology, and a highly skilled and dedicated team of healthcare professionals, Apollo Hospitals is committed to providing quality care and ensuring patient satisfaction in everything we do.


 Our organization strives to offer comprehensive healthcare services across various specialties and disciplines. From primary care to specialized treatments, we provide a wide range of medical services to cater to the diverse needs of our patients. Our hospital is equipped with cutting-edge technology, modern infrastructure, and an experienced team of doctors, nurses, and support staff who collaborate to deliver the highest standards of healthcare.


 At Apollo Hospitals, we believe in fostering continuous learning and innovation. We prioritize research and development to remain at the forefront of medical advancements, enabling us to provide the latest treatments and therapies to our patients. We also emphasize preventive care and wellness programs, promoting a healthy lifestyle and helping individuals maintain optimal health.


 Furthermore, Apollo Hospitals holds a strong commitment to social responsibility. Through various initiatives, we strive to make quality healthcare accessible to all members of society, regardless of their socio-economic background. We actively participate in community health programs, awareness campaigns, and outreach activities to promote healthcare education and support underserved populations.


 As you join our team, we invite you to embody the values and culture of Apollo Hospitals. Our core principles include prioritizing patient-centric care, fostering teamwork, upholding integrity, and embracing compassion in all that we do. Together, we have the power to make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community.


 We are excited about the opportunity to collaborate with you, harnessing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or would like to explore more about Apollo Hospitals, please don't hesitate to contact our team.


 Thank you for joining the Apollo Hospitals family. We are thrilled to begin this journey together, striving for excellence in healthcare.


 Sincerely,


 Team HR

Customer Service Coordinator

Assoc Clinical App SpecAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.<h4>A Day in the Life</h4>Responsibilities may include the following and other duties may be assigned.<ul><li>Conducts on-site education and / or consulting.</li><li>Supports field personnel in providing the best possible outcomes and service for Medtronic customers.</li><li>Partners with sales colleagues to develop and execute plans of sales for within one or more business unit(s).</li><li>Participates in conventions, forums, and meetings to increase product awareness.</li><li>Works closely with Clinical Lead, Clinical Management and Regional Sales team to provide customer case and sales support.</li><li>Identifies and facilitates execution on growth opportunities with Sales and Clinical Support Team.</li><li>Serves as a technical resource to support sales of a specific medical product or solution.</li></ul>SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.DIFFERENTIATING FACTORSAutonomy: Entry-level individual contributor on a project or work team. Works with close supervision.Organizational Impact: Delivers work of limited scope, typically smaller, less complex projects or related activities.Innovation and Complexity: Identifies, defines and addresses problems that are not immediately evident but typically not difficult or complex. Makes minor changes in systems and processes to solve problems .Communication and Influence: Communicates primarily with internal contacts within immediate group. Contacts others to gather, confirm and convey information.Leadership and Talent Management: N / A – job at this level is focused on self-development .Required Knowledge and Experience: Requires broad theoretical job knowledge typically obtained through advanced education. Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A), 0 years of experience required.In the APAC Region Only:•High School Diploma with a minimum of 4 years relevant experiencePhysical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position. <h4>Benefits &amp; Compensation</h4>Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create.  We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. <h4>About Medtronic</h4>We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.  We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&amp;D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.Learn more about our business, mission, and our commitment to diversity <a href="http://www.medtronic.com" rel="noopener noreferrer" target="_blank">here</a>   <h4>Experience Level</h4>Mid Level

India Medtronic Pvt. Ltd

Clinical Informatics Executive

Senior Process Analyst - RCMHuron helps its clients drive growth, enhance performance and sustain leadership in the markets they serve. We help healthcare organizations build innovation capabilities and accelerate key growth initiatives, enabling organizations to own the future, instead of being disrupted by it. Together, we empower clients to create sustainable growth, optimize internal processes and deliver better consumer outcomes. Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new partnerships, clinical services and technology is not enough to create meaningful and substantive change. To succeed long-term, healthcare organizations must empower leaders, clinicians, employees, affiliates and communities to build cultures that foster innovation to achieve the best outcomes for patients. Joining the Huron team means you’ll help our clients evolve and adapt to the rapidly changing healthcare environment and optimize existing business operations, improve clinical outcomes, create a more consumer-centric healthcare experience, and drive physician, patient and employee engagement across the enterprise. Join our team as the expert you are now and create your future.As a Senior Process Analyst, you will be involved in the full lifecycle of RCM. Responsibilities include working in RCM functions like EOB review, Payment Posting, Correspondence review, Bad Debt, Appeals process, Denial management and Account receivables. Strong analytical skills and typing speed is a must. Daily productivity targets to be met. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role.JOB DETAILS: • Good comm skills with neutral accent • Good English Written and Listening skills • Willing to work in US shift timings • Net typing speed of 30 words per min &amp; above with an accuracy rate of 90% + • Good knowledge about MS Office tools • Solve complex scope wise problems with little or no supervision from lead • Interact with key stakeholders • Develop in-depth knowledge of business processes facilitated by our software products • Develop in-depth knowledge of operational processes around the scope of work. • Troubleshoot deployment and environmental issues, resolve issues in a timely manner across multiple projects. QUALIFICATIONS: • 2+ years of industry experience • 2+ year Experience in AR Calling with EPIC is a must. Proficiency in Excel and typing is a must. Familiarity with Cerner applications and other related applications • Ability to adapt quickly to new and changing technical environments as well as strong analytical, problem solving and quantitative abilities. Solid verbal and written communication skills are required. Graduate in Commerce, computer applications . Education/Certifications: • Graduate<h4>Position Level</h4>Senior Analyst<h4>Country</h4>India<h4>Experience Level</h4>Senior Level

Huron Eurasia India Private Limited

Process Analyst

Process Analyst - RCMHuron helps its clients drive growth, enhance performance and sustain leadership in the markets they serve. We help healthcare organizations build innovation capabilities and accelerate key growth initiatives, enabling organizations to own the future, instead of being disrupted by it. Together, we empower clients to create sustainable growth, optimize internal processes and deliver better consumer outcomes. Health systems, hospitals and medical clinics are under immense pressure to improve clinical outcomes and reduce the cost of providing patient care. Investing in new partnerships, clinical services and technology is not enough to create meaningful and substantive change. To succeed long-term, healthcare organizations must empower leaders, clinicians, employees, affiliates and communities to build cultures that foster innovation to achieve the best outcomes for patients. Joining the Huron team means you’ll help our clients evolve and adapt to the rapidly changing healthcare environment and optimize existing business operations, improve clinical outcomes, create a more consumer-centric healthcare experience, and drive physician, patient and employee engagement across the enterprise. Join our team as the expert you are now and create your future.As a Process Analyst, you will be involved in the full lifecycle of RCM. Responsibilities include working in RCM functions like EOB review, Payment Posting, Correspondence review, Bad Debt, Appeals process, Denial management and Account receivables. Strong analytical skills and typing speed is a must. Daily productivity targets to be met. Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role. JOB DETAILS:	 •	Good communication skills with neutral accent •	Good English Written and Listening skills •	Willing to work in US shift timings •	Net typing speed of 30 words per min &amp; above with an accuracy rate of 90% + •	Good knowledge about MS Office tools •	Solve complex scope wise problems with little or no supervision from lead •	Interact with key stakeholders •	Develop in-depth knowledge of business processes facilitated by our software products •	Develop in-depth knowledge of operational processes around the scope of work. •	Troubleshoot deployment and environmental issues, resolve issues in a timely manner across multiple projects.QUALIFICATIONS: • 6 months-2 years of industry experience • 6 months-2 years Experience in relevant billing functions is a must Proficiency in Excel and typing is a must. Familiarity with Cerner applications and other related applications • Ability to adapt quickly to new and changing technical environments as well as strong analytical, problem solving and quantitative abilities. Solid verbal and written communication skills are required. Graduate in Commerce, computer applications . Education/Certifications: • Graduate Must have upto 2 yrs of experience in AR Calling with EPIC.<h4>Position Level</h4>Analyst<h4>Country</h4>India<h4>Experience Level</h4>Senior Level

Sr. Medical Safety AdvisorJob Overview The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the context of the product’s safety profile as well as other products within the same therapeutic area. Also, this position plays a greater role as a senior technical leader and participate in matrix management activities including preparation or participation in evaluating safety issues and preparation of aggregate reports in collaboration with the Post-Marketing Safety Experts and Safety Surveillance Group and be responsible for surveillance activities for selected products.Essential Functions • Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary • Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements • Provide coding review of AEs, SAEs, SADRs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data • Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported • Perform medical safety review of the protocol, Investigative Brochure, and/or Case Report Forms (CRFs) for appropriate safety content and data capture, as applicable • Provide aggregate reviews of safety information, including but not limited to  clinical data, postmarketing, literature review and observational studies to maintain oversight of a product’s safety profile (e.g: DSUR, RMP, PBRER, ad hoc regulatory reports etc) • Ensure service delivery from productivity, compliance and quality perspective within regulatory /contracted timelines. Lead and participate in the initiatives taken for the same from team delivery perspective • Provide therapeutic area/pharmacovigilance issue guidance in the context of leading/managing other safety team members in single case assessment. • Ensure update of watch list, list of expectednsess, labeling list/RSIs etc for the assigned products and develop such additional capabilities within the team • Lead, drive and participate in training activities, product transitions, audit preparation and knowledge exchange initiatives • Review and sign off on the Project Safety Plan and Medical Monitoring Plan per medical safety scope agreed in contract, as applicable • Attend project meetings, medical safety team meetings, and represent safety and clinical data review findings during client meetings, as applicable • Act as Lead Safety Physician, or additional team support, and/or back up on assigned projects as applicable • Provide medical escalation support for medical information and  EU Qualified Persons for Pharmacovigilance projects, as applicable • 24 hour medical support as required on assigned projects • Maintain awareness of medical safety-regulatory industry developments • Provide support and participate in signal detection efforts, e.g. strategy meetings etc. as applicableQualifications • Other A medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Req • Three (3 years) experience practicing clinical medicine after award of medical degree. Graduate, and/or Residency training can qualify for clinical practice experience Req • Two (2) years of pharma experience Pref • Sound knowledge of Medicine • In-depth knowledge of applicable global, regional and local clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines • Knowledge of Pharmacovigilance- ICSR and Aggregate reports • In-depth knowledge of departmental standard operating procedures (SOPs) • Skill in use of multiple safety databases • Adequate Computer skills, especially Microsoft word, excel &amp; PowerPoint • Good communication skills- verbal and written • Ability to establish and maintain effective working relationships with managers, co-workers, investigative site staff, clients and regulatory agency representatives • Ability to establish and maintain effective working relationships with coworkers, managers and clients •  A valid medical license, or equivalent, from the country or region in which he/she resides and works    PrefIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at <a href="https://jobs.iqvia.com/" rel="noopener noreferrer" target="_blank">https://jobs.iqvia.com</a><h4>Experience Level</h4>Senior Level

Safety Coordinator

Assistant Manager, QualAssr-ARPL-AQAQ AR
About Apotex Inc.Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions.For more information visit: <a href="http://www.apotex.com/">www.apotex.com</a>. <h4>Job Summary</h4>Responsible for effective review and approval of Change controls/ Laboratory investigation reports/  Deviations / Lab events/ Corrective action and preventive action (CAPA’s).<h4>Job Responsibilities</h4><ul><li>Review and approval of lab investigation reports (LIR), Deviations, Questionable results, Out of specification (OOS) and Out of trend (OOT) investigations.</li><li>Preparation and review of Standard operating procedures.</li><li>Review and approval of lab events and Temporary changes.</li><li>To review laboratory data with respect to investigations.</li><li>Co-ordinating with cross functional team for the closure of investigations in timely manner.</li><li>Responsible for review and approval in various stages of change controls like QA Acceptance, Change control assessment, QA summary, M-Doc approvals, action item verification &amp; Final closure.</li><li>Co-ordination with regulatory department for regulatory submisssions/Post approval changes.</li><li>Review and approval of CAPA.</li><li>Review of LIR trend reports.</li><li>Responsible for approval of Specification/Certificate of analysis and method of analysis.</li><li>Support to regulatory and customer audits.</li><li>Identify system improvement opportunities for process efficiency.</li><li>Work both independent &amp; as a part of intra/inter departmental teams to ensure that all work is completed in a timely manner to meet compliance.</li><li>Ensure to respond immediately on queries from cross functional teams.</li><li>Approval of reports wherever applicable.</li><li>Work as a member of a team to achieve all outcomes.</li><li>Participate and lead performance conversations with employees, including monthly one on ones, to connect on performance; check in on employee’s progress toward achieving Objectives, offer support and remove barriers; and, communicate and revisit performance expectations to reinforce and encourage high performance culture and a safe working environment for all employees.</li><li>Utilize open, honest, two way communication to build trust-based relationships with employees, business partners and direct leader while continuously improving leadership capabilities by personally seeking feedback and development.</li><li>Create a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values – Collaboration, Courage, Perseverance and Passion.</li><li>Utilize your networks to attract and hire talent in a comprehensive, differentiated and consistent manner essential to our continued growth; then, onboard new employees by providing a consistent experience that reflects the values and commitments made to candidates during the hiring process.</li><li>Ensure adherence of team members (direct reports) with all compliance programs and company policies and procedures.</li><li>All other relevant duties as assigned.</li></ul> <h4>Job Requirements</h4><ul><li>Education
<ul><li>Minimum MSc/B. Pharm degree or any equivalent degree.</li></ul></li></ul><ul><li>Experience
<ul><li>Minium 10 years of experience in GMP regulated pharmaceutical industry.</li></ul></li><li>Knowledge, Skills and Abilities
<ul><li>Good technical knowledge,possess problem solving and logical thinking capabilities.</li><li>Should have competent verbal &amp; written communication skills.</li><li>Proper management skill and leading ability.</li><li>Good leadership quality and communication skill.</li></ul></li></ul> At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. <h4>Experience Level</h4>Mid Level

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