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Rashtrapati Bhavan

Moti Nagar

Vedarth Herbal Time Private Limited

INDOCARE PATHOLOGY LABSJOB FEST - WALKINS (10:30 AM TO 5:30 PM)

CALLING EXECUTIVES FOR MEDICAL SECTOR, 
ANYONE CAN APPLY (10th / 12th PASS / DIPLOMA / ANY GRADUATE)
ONLY 1 ROUND OF INTERVIEW
DIRECT COMPANY HIRING, NO COMMISSION
FRESHER / EXPERIENCED BOTH CAN APPLY
GENDER - MALE / FEMALE (BOTH)
FIXED SALARY + DAILY & WEEKLY INCENTIVES
ELIGIBILITIES - 12th PASS / DIPLOMA / ANY GRADUATE
AGE LIMIT - 18 YRS TO 32 YRS
DOCUMENTS REQUIRED (XEROX ONLY)RESUME (2 COPIES) / 1 AADHAR CARD PHOTOCOPY / 2 PASSPORT SIZE PHOTORECENT /  MARKSHEET


ADDRESS - INDOCARE PATHOLOGY LABS39 - DLF INDRUSTRIAL AREA, 2nd FLOOR, MOTI NAGAR, DELHI - 110015NEAR KIRTI CLUB, CANERA BANK, MATKE WALI GALI AND NEAREST METRO STATION MOTI NAGAR

CONTACT PERSON   (JYOTI - 9319213673)


Indocare Pathology Labs Private Limited

Pharma Forecasting - Senior At 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 Title: Pharma Forecasting Specialist Job Summary: We are seeking a highly skilled Pharma Forecasting Specialist to join our team. This role involves being a key stakeholder in a cross-functional team responsible for forecasting at global, country, and region levels based on need. The ideal candidate will have strong forecasting skills of around 6-8 years, therapeutic area (TA) and pharma experience, and the ability to recommend assumptions, create concept notes, and develop presentations. Basic Python coding skills are also required Roles and Responsibilities: <ul> <li> Develop brand volume forecasts for both short-term and long-term strategic and operational planning. </li> <li> Conduct strategic long-term brand and franchise forecasting, providing guidance based on franchise insights. </li> <li> Solve regional and brand-level analytical challenges using quantitative approaches.• Perform sensitivity analyses to identify opportunities and manage risks, enhancing forecast accuracy. </li> <li> Collaborate as a key stakeholder in cross-functional teams (marketing, finance, MMD, HHI, RCL) for global, country, and regional forecasting needs. </li> <li> Create and maintain accurate forecasts using advanced analytical and forecasting techniques. </li> <li> Recommend assumptions and methodologies for forecasting models. </li> <li> Prepare concept notes and presentations to effectively communicate findings and recommendations. </li> <li> Perform comprehensive business analysis, including requirement elicitation, data management, and change management. </li> <li> Apply Python coding skills to automate and improve forecasting processes. </li> <li> Collaborate with global teams (marketing, finance, RCLs, HHI, MMD, market access) to gather requirements and deliver insights. </li> <li> Analyze historical data and market trends to inform forecasting models. </li> <li> Develop and maintain detailed reports and dashboards for forecasting purposes. </li> <li> Present findings and recommendations to internal stakeholders and executive leadership. </li> <li> Continuously optimize forecasting processes and methodologies. </li> <li> Stay updated with the latest tools, technologies, and best practices in forecasting and analytics. </li> </ul> Key Competencies: <ul> <li> Strong business analysis skills with experience in requirement elicitation, data management, change management, and presentation. </li> <li> Knowledge of Long Range Forecasting process. </li> <li> Excellent communication, facilitation, and stakeholder management skills. </li> <li> Therapeutic area-specific knowledge and pharma experience. </li> <li> Basic Python coding skills. </li> <li> Desired Skills and Experience: </li> <li> Extensive experience in business analysis and forecasting within the pharmaceutical industry. </li> <li> Strong knowledge of one or more pharma therapeutic area such as Oncology, Vaccines etc. </li> <li> Proven track record in developing and maintaining accurate forecasts. </li> <li> Advanced proficiency in business analysis and forecasting tools. </li> <li> Basic proficiency in Python coding. </li> <li> Strong verbal and written communication skills. </li> <li> Ability to manage tasks independently and proactively. </li> <li> Strong analytical and problem-solving skills. </li> <li> Ability to work collaboratively with cross-functional teams and stakeholders. </li> <li> Personal drive and positive work ethic to deliver results within tight deadlines and in demanding situations. </li> </ul> Minimum Qualifications: <ul> <li> Bachelor's degree with relevant work experience in Business Administration, Data Science, Applied Mathematics, Pharmaceutical Sciences, Business Analytics, Computer Science, Information Systems, or other Quantitative field. </li> <li> Experience with tools and techniques like SQL, Tableau, Alteryx, and data processing. </li> <li> Familiarity with Machine Learning/Statistical Learning and AI and their application cases is a plus. </li> </ul> Preferred Qualifications: <ul> <li> Relevant analytical experience in Pharmaceutical Industry. </li> <li> Experience in developing and maintaining forecasting models in the pharmaceutical industry. </li> <li> Expertise in business analysis and forecasting tools. </li> <li> Basic proficiency in Python coding. </li> <li> Strong verbal and written communication skills. </li> <li> Proactiveness and passion to tackle 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.

Ernst & Young LLP ( EY India )

Associate Director Medical InformationJob Description SummaryThe Associate Director, Medical Information is accountable for high-quality medical information documents and responses for assigned assets/disease areas aligned to Therapeutic Areas (TAs). These assets will shape practitioner understanding of Novartis products and support clinical practice. The remit of accountabilities extends to the execution of medical information processes, content and systems, adhering to internal compliance and regulatory requirements. This role must strive to implement industry-leading practices and adopt new technologies in line with emerging medical information standards. Critical to success will be developing productive partnerships with enterprise stakeholders (Biomedical Research, Development, MA/Commercial) for integrative medical information approaches across the complete asset lifecycle – from pipeline/early asset to late-stage/ registration. Job DescriptionAssociate Director Medical Information Location – Hyderabad #LI Hybrid About the Role:The Associate Director, Medical Information is accountable for high-quality medical information documents and responses for assigned assets/disease areas aligned to Therapeutic Areas (TAs). These assets will shape practitioner understanding of Novartis products and support clinical practice. The remit of accountabilities extends to the execution of medical information processes, content and systems, adhering to internal compliance and regulatory requirements. This  role must strive to implement industry-leading practices and adopt new technologies in line with emerging medical information standards. Critical to success will be developing productive partnerships with enterprise stakeholders (Biomedical Research, Development, MA/Commercial) for integrative medical  information approaches across the complete asset lifecycle – from pipeline/early asset to  late-stage/ registration.Key Responsibilities:<ul><li>Develop global medical information strategic and tactical plan for assigned asset/dis[1]ease area.</li><li>Provide direction for content development of medical information Global Guidance  Documents (GGDs). ensuring accuracy, and current with medical literature.</li><li>Provide oversight of global escalation process for medical information inquiries for assigned assets/disease area.</li><li>Conduct review and approval for GGDs and escalated inquiries.</li><li>Support development, maintenance and implementation of policies and procedures for global medical information.</li><li>Evaluate medical inquiries worldwide to identify emerging issues and provide feed[1]back to medical affairs and cross-functional stakeholders on customer insights and  needs.</li><li>Provide guidance and establish best practices in partnership with countries for medi[1]cal information launch readiness.</li><li>Support medical booth at congresses; ensure quality and compliance with all  relevant internal SOPs/guidelines and external regulatory requirements.</li></ul>Commitment to Diversity &amp; Inclusion: We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Essential Requirements:<ul><li>5+ years’ experience in pharmaceutical industry or  healthcare related, ideally in medical affairs and/or medical  information</li><li>Experience in Medical Affairs or Medical Information solutions and demonstrated innovation in processes/technical approaches</li><li>Understanding of the role of medical information and key  needs of customers</li><li>Excellent written/oral communication skills and strong understanding of medical writing customers</li><li>Ability to provide strategic insight into medical information  that support launch assets.</li><li>Thorough understanding of internal/external ethical guide[1]lines relevant to the pharmaceutical industry.</li><li>Strategic mindset including innovation and critical thinking  with performance-oriented drive.</li></ul> Desirable Requirements:<ul><li>Strong written and communication skill.</li><li>Experience working in a matrix environment, across functions,  therapeutic areas, regions and countries.</li></ul>Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Skills DesiredClinical Research, Clinical Trials, Detail-Oriented, Medical Writing, People Management, Regulatory Compliance, Safety, Waterfall Model<h4>Experience Level</h4>Mid Level

Novartis India

Job Posting Title Associate, Managed Access Programs (MAP) & Post-Study Drug Supply (PSDS) OperationsJob Description SummaryJoin Novartis as an Associate, Managed Access Programs (MAP) &amp; Post-Study Drug Supply (PSDS) Operations and play a key role in supporting patient access to innovative therapies. You will contribute to the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them - efficiently, compliantly, and with high quality. Your commitment to operational excellence and attention to detail will help simplify processes and uphold the highest standards, making a meaningful impact on patients and healthcare. Job DescriptionAssociate, Managed Access Programs (MAP) &amp; Post-Study Drug Supply (PSDS) Operations Location – Hyderabad #LI HybridAbout the Role:Join Novartis as an Associate, Managed Access Programs (MAP) &amp; Post-Study Drug Supply (PSDS) Operations and play a key role in supporting patient access to innovative therapies. You will contribute to the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them - efficiently, compliantly, and with high quality. Your commitment to operational excellence and attention to detail will help simplify processes and uphold the highest standards, making a meaningful impact on patients and healthcare.Key Responsibilities:<ul><li>upport completion of MAP and PSDS strategy plans with input from cross-functional teams.</li><li>Assist with operational setup, maintenance, and closure of assigned MAP and PSDS programmes.</li><li>Support development, review, submission, maintenance, and archival of MAP and PSDS documents in relevant systems.</li><li>Contribute to product and budget forecasts for MAP and PSDS, supporting review and updates throughout programme lifecycle.</li><li>Support oversight of the drug supply process for assigned programmes.</li><li>Assist with input to safety update reports (DSUR/PSUR) as applicable for MAP and PSDS activities.</li><li>Support preparation of presentations and documentation to secure operational and financial endorsement.</li><li>Help identify, track, and manage risks and issues, proposing mitigation strategies in collaboration with stakeholders.</li><li>Collaborate with global and local partners to deliver MAP and PSDS operational activities efficiently and compliantly.</li><li>Maintain real-time data accuracy in relevant systems and support audit preparation and corrective actions.</li></ul>Commitment to Diversity &amp; Inclusion: :We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Essential Requirements:<ul><li>Master’s degree in science or clinical operations.</li><li>Approximately 3 years’ relevant experience in the pharmaceutical industry or public health sector.</li><li>Basic knowledge of medical affairs, clinical operations, or drug development.</li><li>Experience working in global matrix teams and project environments.</li><li>Good interpersonal and communication skills across diverse audiences and organisational levels.</li><li>Organised, detail-oriented, and able to work with minimal supervision.</li><li>Proficient in Microsoft tools, including SharePoint, Teams, Excel, PowerPoint, and document management systems.</li><li>Excellent English language skills, both written and spoken.</li></ul> Desirable Requirements:<ul><li>Ability to build relationships with internal and external stakeholders, demonstrating adaptability to change.</li><li>Openness to change and commitment to promoting a culture of high ethical standards and compliance.</li></ul>Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Skills DesiredClinical Trials, Conflict Management, Contract Management, Effective Communication, Financial Analysis, Negotiation Skills<h4>Experience Level</h4>Mid Level

Manager, Managed Access Programs (MAP) & Post-Study Drug Supply (PSDS) OperationsJob Description SummaryJoin Novartis as a Manager, Managed Access Programs (MAP) &amp; Post-Study Drug Supply (PSDS) Operations and play a key role in managing patient access to innovative therapies. You will manage the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them - efficiently, compliantly, and with high quality. Your commitment to operational excellence and attention to detail will help simplify processes and uphold the highest standards, making a meaningful impact on patients and healthcare. Job DescriptionManager, Managed Access Programs (MAP) &amp; Post-Study Drug Supply (PSDS) Operations Location – Hyderabad #LI HybridAbout the Role:Join Novartis as a Manager, Managed Access Programs (MAP) &amp; Post-Study Drug Supply (PSDS) Operations and play a key role in managing patient access to innovative therapies. You will manage the planning and execution of these programs, collaborating with global teams to ensure medicines reach those who need them - efficiently, compliantly, and with high quality. Your commitment to operational excellence and attention to detail will help simplify processes and uphold the highest standards, making a meaningful impact on patients and healthcare.Key Responsibilities:<ul><li>Coordinate completion of MAP and PSDS strategy plans with input from cross-functional teams.</li><li>Support operational setup, maintenance, and closure of assigned MAP and PSDS programmes, ensuring oversight.</li><li>Develop, review, submit, maintain, and archive MAP and PSDS documents in relevant systems.</li><li>Provide product and budget forecasts for MAP and PSDS, updating regularly and escalating changes for approval.</li><li>Manage and maintain oversight of the drug supply process for assigned programmes.</li><li>Contribute to safety update reports (DSUR/PSUR) as applicable for MAP and PSDS activities.</li><li>Prepare presentations and supporting documentation to secure operational and financial endorsement.</li><li>Identify, track, and manage risks and issues, proposing mitigation strategies and escalating as needed.</li><li>Collaborate with global and local partners to deliver MAP and PSDS operational activities efficiently and compliantly.</li><li>Support global inspection and audit preparation, conduct quality and internal audits, and assist with corrective actions.</li></ul>Commitment to Diversity &amp; Inclusion: :We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.Essential Requirements:<ul><li>Master’s degree in science; Doctor of Medicine or Pharm D. is a plus.</li><li>Minimum 5 years’ relevant experience in the pharmaceutical industry or public health sector.</li><li>Strong knowledge of medical affairs, clinical operations, or drug development.</li><li>Demonstrated ability to work effectively in global matrix teams and project environments.</li><li>Excellent interpersonal and communication skills across diverse audiences and organisational levels.</li><li>Highly organised, detail-oriented, and able to work independently with minimal supervision.</li><li>Proficient in Microsoft tools, including SharePoint, Teams, Excel, PowerPoint, and document management systems.</li><li>Excellent English language skills, both written and spoken.</li></ul> Desirable Requirements:<ul><li>Experience in working within global organizations and project teams, demonstrating adaptability to changing environments.</li><li>Openness to change and ability to promote a culture of high ethical standards and compliance.</li></ul>Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Skills DesiredBuilding Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)<h4>Experience Level</h4>Mid Level

Chief Medical Information Officer

 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>Executive Level

Apollo Hospitals Enterprise Limited

Genpact

Senior Scientist Clinical PharmacokineticsJob Title: Senior Scientist Clinical PharmacokineticsGlobal Career Level: DIntroduction to roleAre you ready to follow the science and explore new frontiers in clinical pharmacokinetics? As a Senior Scientist in Clinical Pharmacokinetics, you will design and review clinical pharmacology study protocols, conduct non-compartmental pharmacokinetic analyses using Phoenix/WinNonlin software, and prepare comprehensive clinical study reports. Collaborating closely with Clinical Pharmacologists, Bioanalysts, Programmers, Statisticians, and Clinical Research Organizations, you will play a pivotal role in preparing regulatory submissions and documentation related to non-compartmental pharmacokinetics. Join us in our mission to unlock the power of science and make a difference in patients' lives.Accountabilities- Provide pharmacokinetic (PK) methodology for inclusion in analysis plans and clinical protocols or analysis plans. - Produce pharmacokinetic tables, figures, and listing shells to detail the planned presentation of results. - Review draft tables, figures, and listings to finalize their format. - Create associated datasets. - Conduct non-compartmental analyses (NCA), interpretation, and reporting of pharmacokinetic and pharmacodynamic (PD) data using appropriate software like Covance’s Phoenix WinNonlin system (Pharsight). - Collaborate with bioanalysis vendors for interim analysis to ensure timely data transfers and resolve data queries. - Perform pharmacokinetic (and pharmacodynamic) analysis for interim analysis to support dose progression. - Interpret and prepare the pharmacokinetic component of Clinical Interpretation Meeting materials. - Write the pharmacokinetic sections of clinical study reports and scientific manuscripts. - Review technical validity of non-compartmental analyses performed by peers as quality control. - Assist in developing departmental guidelines, processes, software, and training materials for non-compartmental analysis. - Train and mentor other pharmacokinetists based on experience. - Support Manager and Clinical Pharmacologists with Health Authority queries. - Prepare submission documentation and other documents for Health Authorities related to non-compartmental pharmacokinetic analyses.Essential Skills/Experience- Bachelor’s degree in Science or Pharmacy - 6-10 years experience in pharmacokinetic data analysis (i.e. Phoenix WinNonlin or similar) and report writing. - Knowledge of regulatory agency guidelines. - Effective time management and organizational skills.Desirable Skills/Experience- Experience with PK-PD modeling - Team player works with others respectfully and cordially. - The ability to adapt, work through conflicts, and persuasively influence outcomes. - Effectively cope with change and is comfortable changing direction and acting without complete information. - Ability to develop and deliver effective presentations and written/oral communications. - Thrives in a fast-paced business environment. - Good oral and written English language fluency.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 our passion for science and our commitment to making a difference. We are dedicated to treating, preventing, modifying, and even curing some of the world's most complex diseases. By fusing data and technology with scientific innovations, we aim to achieve breakthroughs that positively impact billions of patients worldwide. Our inclusive environment encourages collaboration across academia, biotechs, and industry, allowing us to create swift impacts on disease. Here, curiosity thrives as we explore without limits, empowered to make bold decisions.Ready to make an impact? Apply now to join our team at AstraZeneca!Date Posted25-Sept-2025Closing Date05-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>Senior Level

Astrazeneca India Private Limited

Group Lead, Medical CommunicationsJob Description SummaryTo achieve excellence in scientific communication by providing operational and compliance support while delivering high quality medical communication assets (publication and medical education) ensuring consistent and appropriate coordination with the US TA Medical Communications Leads. Job DescriptionPosition SummaryTo achieve excellence in scientific communication by providing operational and compliance support while delivering high quality medical communication assets (publication and medical education) ensuring consistent and appropriate coordination with the US TA Medical Communications Leads.Responsibilities include:<ul><li>Provides single point of contact between USMA Med Comms and Novartis Corporate Center (NoCC). Acts as a liaison with and helps maintain highest standards for publications, MSL tools, congress content and other medical education deliverables.</li><li>Works proactively with scientific writers for implementing deliverables and brand-specific internal or external style guidelines, copyediting, language editing, and proofreading of scientific communication deliverables</li><li>Ensures compliance with Novartis and Medical Communication's specifications, project management standards, and policies for assigned therapeutic areas. Ensures timely communication and follow-up with the team members to prepare team for compliance readiness.</li><li>Complies with audit and standard operating procedure (SOP) training requirements. Works with manager - operations to conduct process audit, measure training compliance, and compliance with workload tracker.</li><li> Develops report and presents recommendations to the leadership team to improve compliance. Conducts periodic quality checks to ensure accuracy and compliance with internal and external publication and communication standards for assigned therapeutic areas (such as Good Publication Practice, Sunshine Act).</li><li>Assist in the development or update of departmental SOPs, working practices, or processes. Lead publication excellence projects of medium complexity and implement changes. Leads operational initiatives to enhance quality of work, reduces cycle time, and improves compliance. Shares observations, ideas, and feedback based on interactions with the team to bring process improvements.</li><li>Leads a team of 30 - 50 FTEs ensuring delivery of medical communications deliverables for US Medical Affairs. Codevelops KPIs. Monitors and reports established KPIs for the team. Takes proactive action to continuously strive for process/quality improvements. Sets direction, aligns and motivates team members to achieve set goals and objectives.</li><li>Supports resource planning, workload distribution, budget input, cost reporting, and tracking demand for work. Supports new technologies and digital communication channels for future readiness. Owns, contributes and ensures deployment and completion of initiatives, programs and AI/Automation opportunities across content development towards creating scientific and functional excellence. Recruits' talent manages performance (set objectives, review performance and plan compensation) and develops associates.</li></ul>Essential Requirements<ul><li>Minimum: B.Sc./equivalent or M.Sc./M.Pharm with commensurate experience.</li><li>Preferred: Doctoral Degree in Medical Sciences; preferably in healthcare-related field.</li><li>5 -10 years medical affairs experience. 3-5 years medical communications experience.</li><li>Ability to work in a highly matrixed environment with multiple stakeholders.</li><li>Strong written and verbal communication skills.</li><li>Working knowledge of US Healthcare landscape knowledge.</li><li>Travel internationally/domestically as required.</li><li>Ability and willingness to work off hours and holidays if required.</li></ul>Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture  You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards  Commitment to Diversity and Inclusion:   Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.   Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network. Skills DesiredAgility, Agility, Clinical Practices, Cross-Functional Collaboration, Data Analysis, Drug Development, Employee Development, Healthcare Sector Understanding, Health Sciences, Influencing Skills, Innovation, Inspirational Leadership, Integrated Evidence Generation, Medical Affairs, Medical Communication, Medical Education, Patient Care, People Management, Pharmaceutics, Priority Disease Areas Expertise, Product Launches, Product Strategy, Real World Evidence (RWE), Regulatory Compliance, Research Methodologies {+ 3 more}<h4>Experience Level</h4>Senior Level

Senior Associate, Field Medical Excellence Operations<h4>Career Category</h4>Operations<h4>Job Description</h4>About Us: Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.Role Description: The Field Medical Excellence Operations Associate Manager supports core operational activities that enable Amgen’s Field Medical teams to operate efficiently and effectively. This role focuses on reporting, user support, system documentation, and CRM maintenance, contributing to Amgen’s mission of scientific excellence through high-quality operational delivery.Reporting to the Manager or Senior Manager of Field Medical Excellence Operations, this position provides hands-on execution of training development, system testing, SharePoint management, and documentation activities. This individual will contribute to the buildout of analytics, platform adoption, and user engagement.Roles and Responsibilities:<ul><li>Execute routine support activities for CRM platforms (Veeva/Salesforce) and reporting tools.</li><li>Automate recurring tasks by identifying opportunities, developing and maintaining solutions, and ensuring efficiency, reliability, and compliance with organizational standards.</li><li>Develop and maintain training materials (QRGs, FAQs, manuals, and videos) to support end users.</li><li>Manage mailboxes, portals, and user requests globally, ensuring timely resolution and documentation.</li><li>Contribute to system enhancement projects through testing, impact assessment, and documentation.</li><li>Support ad hoc stakeholder requests, report generation, and data validation.</li><li>Build wireframes and mockups for new system features and reporting capabilities.</li><li>Perform basic data auditing and validation to support CRM data quality.</li><li>Support internal and external country specific audits with accurate data with regulatory standards and company policies.</li><li>Develop SharePoint-based tools and documentation in alignment with internal standards.</li><li>Assist in designing and documenting CRM processes, business workflows, and system integrations.</li><li>Participate in user training and onboarding activities for new field users.</li><li>Collaborate with cross-functional teams (e.g. Medical Data and Analytics, training, and IS partners) on platform continuity and updates.</li></ul>Basic Qualifications and Experiences:Advanced scientific degree:<ul><li>Bachelor’s degree &amp; 6 years of directly related industry experience OR</li></ul><ul><li>Associates degree &amp; 8 years of directly related industry experience </li></ul>Functional Skills:Preferred Qualifications:<ul><li>Foundational understanding of medical systems operations (MSO)</li><li>Experience in report development using analytical tools such as Tableau or Smartsheet</li><li>Proficiency in Microsoft Excel (data analysis, reporting, automation) and PowerPoint (presentation development and storytelling)</li><li>Familiarity with SharePoint design, testing, and documentation</li><li>Strong written communication and technical documentation skills</li><li>Experience in training content development and system documentation</li><li>Exposure to system testing, QA, and validation practices</li><li>Knowledge of system lifecycle management and basic IT governance</li><li>Detail-oriented with a strong sense of ownership and follow-through</li></ul>Competencies:<ul><li>Execution &amp; Delivery: Executes tasks accurately and efficiently, ensuring consistency and adherence to process requirements and timelines.</li><li>Learning Agility: Quickly learns new tools, systems, and procedures while seeking feedback and applying it to improve performance.</li><li>Documentation &amp; Communication: Demonstrates clarity in documentation, process summaries, and training materials; communicates effectively within the team.</li><li>Attention to Detail: Maintains high standards in documentation, testing, and data quality efforts, reducing errors and rework.</li><li>Team Collaboration: Contributes to a team-oriented environment; is receptive to direction and collaborates well with others.</li><li>Service Orientation: Responds to end-user needs and ad hoc requests in a timely and helpful manner, fostering trust and reliability.</li><li>Initiative: Proactively identifies gaps or issues and surfaces them to management, offering suggestions or potential improvements.</li><li>Adaptability: Adjusts to changes in project scope, technology, and priorities with a flexible and positive attitude.</li></ul>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation..<h4>Experience Level</h4>Senior Level

Amgen Technology Private Limited

Healthcare Product Manager_Q2•	Payer/ Provider/ PBM organizations
•	Product Management/Product Engineering /Healthcare Operations 
•	Experience working with industry leading Enrollment, Claims, Billing or EHR systems.
•	Managing product lifecycle in whole – from ideation, exploration, approval, development, implementation, measurement, and ongoing development.
•	Expertise in US Government Program Line of Business - Medicare, Medicaid, Duals, Marketplace
•	Plan Sponsor &amp; Product, Enrollment &amp; Billing, Provider Data Management, Provider Network Management, Claims, Encounters, Medicare, and Marketplace Risk Adjustment.
•	Developing results-oriented strategies to solve complex and open-ended business problems.
•	Market Analysis and Product fitment
•	Communicating and facilitating architecture design discussions/decisions and impacts to key stakeholders.
•	Customer success on managing customer engagements and requirements.
•	Leading business pursuits and product demonstrations.
•	Agile Product Development Methodology •	Experience in market leading healthcare products (key emphasis).
•	Proven track record of at least 8 years in software product management roles.
•	Capability/Feature planning and design, manage the specifications of their development, and monitor their on-going operation to better understand customer experiences.
•	Clearly communicating progress towards delivery, technical challenges that may occur.
•	Act as a thought leader and subject matter expert in the assigned product area, develop essential product documentation including business case, business requirements and use cases.
•	Own product backlog and collaborate closely with the platform engineering team.
•	Create Journey Maps that re-imagine/re-define the healthcare problematic process areas.
•	Understanding of trends affecting customer adoption.
•	Experience of working with enterprise customers, both technical and business, and at all levels.
•	Influence leaders in diverse functional areas
•	Strong business acumen including experience in estimation and pricing, market research. 
•	Demonstrated ability to navigate ambiguity and adapt quickly to modern technology and processes.
•	Strong analytical ability with exposure to data science and automation
•	Teaming/Collaboration - Demonstrates exceptional leadership and team management skills, with a collaborative and empowering approach to achieve results through influence.
•	Excellent communication, presentation, and interpersonal skills to develop lasting relationships with senior business or technical leaders with the highest levels of business acumen and technical expertise. As a ‘Senior Product Manager’ you will be pivotal to creating roadmap, owning release plan for multiple capabilities that is futuristic and meets industry and client needs. You will be responsible for continuous backlog management, prioritizing the backlog considering the needs and objectives of every stakeholder. As a thought leader in your business domain, bring in industry best practices, learnings from client demos and interactions into designing. You will anchor business pursuit initiatives, sales demo. You will have the opportunity to shape the Infosys platform that enables payers and providers to deliver better care.

Infosys

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