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Sr. Executive <ul><li>Qualification - M.sc/ B. Pharm/ M.Pharm</li><li>Department - QC (Micro)</li><li>Work Experience - 7-15 years</li></ul> Share your updated resume now.

Coral Drugs Pvt Ltd

Senior Executive

Staff Nurse - Nursing

 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>Senior Level

Apollo Hospitals Enterprise Limited

Staff Nurse

Cssd Assistant - Central Sterile Supply Department (CSSD)

 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

Healthcare Assistant

Flow cytometry Data analyst<h4>Responsibilities</h4><ul><li>Analyze Flow Cytometry Patient and Quality Control Data</li><li>Address Data Inquiries and Investigations</li><li>Data Entry, Resulting and Release into clinical database</li><li>Draft and review standard operating procedures (SOP)</li><li>Sophisticated instrument troubleshooting</li><li>Reagent qualifications</li><li>Participation in validation of new assays working closely with our scientific team</li><li>Interact with clients and internal stakeholders on data troubleshooting</li></ul>Education/ Qualification:<ul><li>Bachelor or Master degree in Biomedical sciences, Biological sciences Medical Technologist, Medical Lab Technology (medische laboratoriumtechnologie)</li><li>1-3 years experience in a similar role or in a lab environment</li><li>Experience with Flow Cytometry with emphasis on data analysis is seen as advantage!</li><li>Preferably experience with analysis of Flow Cytometric data</li><li>Experience in data analysis with WinList, FlowJo, FCSExpress, etc. is preferred</li><li>Significant experience with Microsoft Excel is also preferred</li><li>Ability to read and understand Standard Operating Procedure in English</li><li>Born problem solver with an eye for detail and customer oriented attitude</li><li>Ability to work under pressure and analytical mindset</li><li>Good communication skills are required</li><li>Fluency in English, Dutch and French are seen as an advantage</li></ul>Labcorp is proud to be an Equal Opportunity Employer:Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to applyIf you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our <a href="https://careers.labcorp.com/global/en/accessibility" rel="noopener noreferrer" target="_blank">accessibility site</a> or contact us at <a href="mailto:Disability_apply@LabCorp.com" rel="noopener noreferrer" target="_blank">Labcorp Accessibility.</a> For more information about how we collect and store your personal data, please see our <a href="https://www.labcorp.com/about/web-privacy-policy" rel="noopener noreferrer" target="_blank">Privacy Statement</a>.<h4>Experience Level</h4>Mid Level

LabCorp

Medical Laboratory Assistant

Nursing 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

Nursing Superintendent

Consultant - General SurgeryJob Purpose                                  Qualification:Graduate; 1st division in 10th, 12th and GNM Nursing/BSc Nursing/M.Sc Nursing Relevant Experience:    3 months – 5 years of experience in field of Nursing assessing patient’s health problems, providing care to sick, disabled, recovering or injured patients, maintaining important medical records, implementing a nursing care plan and advising patients about maintaining health. Responsibilities<ul><li>Recording medical history and symptoms</li><li>Administering medication and treatment</li><li>Collaborating with teams for patient care</li><li>Performing point of care tests</li><li>Conducting nursing assessment</li><li>Monitoring patient’s health</li><li>Providing support and education to patient and family</li><li>Maintaining inventory</li><li>Providing bedside care</li><li>Operating and care of medical equipment</li><li>Attending regular in-service education</li></ul>Requirements and skills<ul><li>Interpersonal relationship skills</li><li>Listening</li><li>Team building</li><li>Perceptual</li><li>Communication</li><li>Coordination and cooperation</li><li>Initiative</li><li>Moral support and physical approach to patient</li><li>Computer literacy</li><li>GNM Nursing/BSc Nursing/M.Sc Nursing</li></ul> 


 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

General Physician

Registered Nurse - Nursing

 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

Registered Nurse

Info Specialist - Asset Rights ManagementJob Description SummaryEnsure timely, compliant, and high-quality access to scientific and medical literature by managing document delivery and copyright permissions in support of regulatory and business needs. Serve as a first point of contact for NKC InfoDesk enquiries, providing guidance and resolution tracking. Through efficient sourcing, permissions handling, and user support, contribute to the responsible use of information assets and enable informed decision-making across Novartis Job DescriptionInfo Specialist - Asset Rights Management Location – Hyderabad #LI Hybrid About the Role:Ensure timely, compliant, and high-quality access to scientific and medical literature by managing document delivery and copyright permissions in support of regulatory and business needs. Serve as a first point of contact for NKC InfoDesk enquiries, providing guidance and resolution tracking. Through efficient sourcing, permissions handling, and user support, contribute to the responsible use of information assets and enable informed decision-making across Novartis.Key Responsibilities:<ul><li>Carry out basic database searches to verify bibliographic citations </li><li>Get the subscribed materials online and ensure that they are accessible. Escalate access issues and broken links. </li><li>Obtain material not held in Novartis Knowledge Center collection, selecting the best possible option</li><li>Copyright permissions are verified under license / terms of use and laws. </li><li>Independently handle incoming customer requests, escalate items if not re-solved. </li><li>Provide learning programs and front-line guidance to users. </li><li>Use InfoDesk Tracking system (ATT) to ensure proper tracking and resolution. </li><li>Conduct Asset Rights Management projects, as required. </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 or equivalent degree/diploma in Library and Information Science.</li></ul><ul><li>At least 3-5 years of experience with interlibrary loan / document delivery including verification of bibliographic citations and location of items required. </li></ul><ul><li>Experience practicing intellectual property law required, specifically in the areas of copyright and licensing will be an added advantage. </li></ul><ul><li>Proven experience in customer service, preferably in a library environment. </li></ul><ul><li>Broad knowledge of healthcare online tools and e-resources (database, e-journals, etc.) </li><li>A keen interest in, and enthusiasm for, developments in library and information science.  </li><li>Attention to detail with the ability to complete a large volume of work quickly and independently</li></ul>Desirable Requirements:<ul><li>Excellent written and oral English skills are required. Additional language skills advantageous. </li><li>Ability to collaborate with global colleagues </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, Safety<h4>Experience Level</h4>Mid Level

Novartis India

Asset Operations Administrator

Senior Clinical Database DeveloperJob Description Summary-Provide timely &amp; professional ongoing Mgmt of Data Mgmt/Coding/CDDRA-Database Development/DAP deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials within Clinical Data Mgmt. Ensure consistently high quality data available for analysis and reporting. Develop content and redefine training modules into engaging &amp; interactive applications. Leverage technology to ensure process simplification and training delivery. Follows Good Clinical Practices (GCP), data-handling procedures and guidelines. Participates in the review of clinical research protocols, reports and statistical analysis plans. Drives participation and input within Data Operations (DO) in the delivery of quality data and programs, processes and documentation -Manage data Load, Transfer and conform of Clinical trial data to NCDS compliant standards. The position is a key contributor with Data Provisioning team in ensuring that pharmaceutical drug-development plans in Novartis Global Drug Development are executed efficiently with timely and high quality deliverables. Job DescriptionMajor accountabilities: <ul><li>Provides DM leadership across assigned trial (s) and Acts as the Trial Data Manager where needed -Demonstrates a business understanding of the compound (s) profile to identify and assist in successful application of data Mgmt processes.</li><li>Provides feedback to assure well written protocols and amendments.</li><li>Recognize and resolve protocol issues that may impact database design, data validation and /or analysis/reporting and that do not make the best use of available standards -Performs DM activities for start up of a study, Data Handling plan , Data Review Plan and performing user acceptance testing (UAT) -Manage local lab set up for the Clinical Database as applicable -Leads process and training deliverables within platform or processes.</li><li>Accountable for all aspects of the Process and Training within remit to ensure full compliance to all applicable global regulatory requirements is maintained and business objectives are achieved.</li><li>Accountable for all quality related aspects -Centralizes and aligns DO for audits and inspections.</li><li>Manages and measures Quality -Coordinates exception requests, deviations and corrective /preventative action plans -Performs DM hands on activities during the course of the study Performs ongoing review of all data generated from the clinical study including Third party and local lab data as well as SAE reconciliation where applicable -Responsible and accountable to ensure consistency of assigned trials with program level standards across DM documentation -Has proven abiity to use the tools available to generate listings for data review and where necessary provides these to the study teams.</li><li>Generates the study status reports for use at Clinical trial team meetings.</li><li>Supports and assists Junior staff for assigned trials -Provides effective input into DM initiatives and innovations for quality, efficiency and continuous improvement in scientific and operational excellence -Leads /Coordinates synonym review activities and dictionary version upgrade activities at trial /Program level.</li><li>Serves as primary study lead ensuring timely and quality deliverables by establishing and maintaining strong working relationships with study teams, and functional lines.</li><li>Acts as a technical consultant as required.</li><li>Lead DAP activities for assigned /Project level activities for phase I to IV clinical studies in Novartis Global Drug Development.</li><li>Lead independently or participate in improvement initiatives and /or nonclinical projects.</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)</li></ul>Key performance indicators: <ul><li>Achieve high level of quality, timeliness, cost efficiency and customer satisfaction across Data Mgmt activities and deliverables.</li><li>No critical audit findings due to Data Mgmt -Adherence to Novartis policy and guidelines -Customer / partner/ project feedback and satisfaction</li></ul>Minimum Requirements: Work Experience: <ul><li>Cross Cultural Experience.</li><li>Functional Breadth.</li><li>Project Management.</li></ul>Skills: <ul><li>Clinical Data Management.</li><li>Data Governance.</li><li>Data Integrity.</li><li>Data Management.</li><li>Data Quality.</li><li>Data Science.</li><li>Databases.</li><li>Project Management.</li></ul>Languages :<ul><li>English.</li></ul> Skills DesiredClinical Data Management, Databases, Data Governance, Data Integrity, Data Management, Data Quality, Data Science, Waterfall Model<h4>Experience Level</h4>Senior Level

Clinical Informatics Executive

Senior 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

IQVIA

Safety Coordinator

Associate Manager, Clinical Data ManagementJob Overview Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements.Essential Functions • Manage a team of professional Data Management staff. Size of team could vary from 4+ upwards -8, depending on the Data Management Function. Define resource requirements and work with supervisor to prioritize resource assignments across projects. Directly responsible for utilization of staff. Assess and document competency of staff to satisfy position responsibilities. Regularly set goals and evaluates and documents performance. Propose promotion and termination actions. Participate in recruitment of new staff. Implement department/office objectives. Provide review and guidance for production of Data Management documentation or deliverables that are produced by the Data Management Function. For example, an Associate Manager of Clinical Data Programming would provide expert review and guidance for database design and set-up, validation definition and programming, and database deliverables to internal and external customers. Provide technical advice and solutions with internal and external customers to solve problems and improve efficiency. Participate in the implementation of new processes and technology. Ensure that staff is trained and compliant with current operating procedures and work instructions and project scope of work. Identify and address professional development/training needs of staff. Mentor staff members to develop Data Management process and system expertise. Primary customer interactions at project level with a focus on specific Data Management Function. With established customers, provide operational input into proposals and scope of work • participate in proposal defenses. May participate in customer meetings and lead discussions of project requirements and strategic planning. Understand scope of work, budget, and scope assumptions. Identify out of scope work and contribute to estimating costs of this work. Ensure project milestones pertaining to Data Management Function are met according to agreed upon timelines with high quality. May spend significant time performing work tasks associated with Data Management Function, typically in a lead role. Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work • appraising performance and guiding professional development • rewarding and disciplining employees • addressing employee relations issues and resolving problems. Approve actions on human resources matters.Qualifications • Bachelor's Degree Clinical, biological or mathematical sciences or related field, or nursing qualification Req • 9-15 years of relevant work experience in Clinical Data Management.• Equivalent combination of education, training and experience. • Advanced knowledge of Data Management processes and systems. Broad understanding of clinical drug development process. Good oral communication skills.• Excellent organizational skills and demonstrated ability to manage projects. Effective problem solving skills. Proven leadership skills.• Ability to establish and maintain effective working relationships with coworkers, managers and clients. Advanced knowledge of Data Management processes and systems.• Broad understanding of clinical drug development process. Good oral communication skills. Excellent organizational skills and demonstrated ability to manage projects.• Effective problem solving skills.•Proven leadership skills. Ability to establish and maintain effective working relationships with coworkers, managers and clients.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>Mid Level

Associate Director Evidence GenerationJob Description Summary#LI-Hybrid Location: Hyderabad, India Step into a role where your scientific expertise can shape the future of medicine. As Associate Director of Evidence Generation, you’ll lead the development of innovative, non-interventional studies and Real-World Evidence programs that influence global healthcare decisions. You’ll collaborate with cross-functional teams and external stakeholders to deliver impactful, fit-for-purpose evidence that supports access, adoption, and optimal use of Novartis medicines. This is your opportunity to reimagine how evidence drives patient outcomes and regulatory success and make a meaningful difference in the lives of millions. Job Description<h4>Key Responsibilities</h4><ul><li>Lead design and execution of non-interventional studies aligned with Integrated Evidence Plans</li><li>Develop study concepts, protocols, reports, and contribute to final analyses and publications</li><li>Ensure scientific rigor and relevance in evidence strategy, study design, and data interpretation</li><li>Engage with global stakeholders including key opinion leaders, advisory boards, and patient groups</li><li>Represent Novartis in external collaborations and lead/co-chair steering committees for studies</li><li>Support development of innovative methodologies and technologies to enhance evidence generation</li><li>Stay current with trends and drive adoption of emergent evidence approaches across teams</li></ul><h4>Essential Requirements</h4><ul><li>Advanced degree in life sciences or healthcare; MBA or equivalent preferred</li><li>10+ years of experience in pharma, academic research, or healthcare with focus on evidence generation</li><li>Strong expertise in non-interventional study design and Real-World Evidence methodologies</li><li>Proven ability to communicate complex scientific concepts to diverse internal and external audiences</li><li>Demonstrated success working in cross-functional, global matrix environments</li><li>Excellent collaboration, organizational, and strategic thinking skills</li></ul> 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>Mid Level

Senior Associate

Associate Director Medical Information Group LeadJob Description SummaryThis role is accountable for managing and leading a Medical Information delivery team to produce high- quality medical information documents and responses Job DescriptionAssociate Director Medical Information Group Lead Location – Hyderabad #LI Hybrid About the Role:This role is accountable for managing and leading a Medical Information delivery team to produce high-quality medical information documents and responsesKey Responsibilities:<ul><li>Responsible for the performance of the assigned Medical Information team to deliver as designed with quality, timeliness and in a compliant manner.</li><li> Track progress and identifies improvement opportunities and best practices. Ensure that best practices are shared across the Medical Information delivery teams.</li><li>Co-ordinate capacity and workforce planning for assigned programs and deliverables, to ensure adequate assignment of resources to meet business needs.</li><li>Drive functional excellence and consistency in delivery.</li><li>Stakeholder Management – identify, engage and manage stakeholder expectations.</li><li>Escalation point for issues and ensure effective and efficient resolutions, initiating and leading remediation plans where appropriate.</li><li>Supports operational governance and business planning with standardization of processes, ensuring quality and compliance with all relevant internal SOPs/guidelines and external regulatory requirements.</li><li> Responsible for recruiting and retaining talent, managing performance, and developing associates. Responsible for developing high performing teams in a constructive culture. · Ensure compliance and inspection /audit readiness.</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>Advanced degree (PhD, PharmD, MD) in life science/healthcare or relevant experience. Desirable: MBA</li><li>&gt;10 years of pharmaceutical industry experience in Medical Information ·</li><li>&gt;/= 3 years of people management experience ·</li><li>Proven track record in customer delivery environments and experience with the development of MI services in shared service centers .</li><li> Deep understanding of good practices in medical enquiry management, medical information writing, and medical content review Experience with developing, implementing and maintaining processes that adhere to company, industry and HA requirements ·</li><li>Superior people management skills with demonstrated positive leadership, innovative and collaborative behaviors · Proven ability in interpersonal, communication, negotiation and diplomacy skills. Demonstrated influencing and leadership skills in an international matrixed environment.</li></ul>Desirable Requirements:<ul><li>Demonstrated success in resource (budget and headcount) planning and management.</li><li>Strong financial and business acumen</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>Mid Level

Medical Record / Health Informatics Executive

Associate Director Evidence Partnerships & SolutionsJob Description Summary#LI-Hybrid Location: Hyderabad, India Are you ready to reimagine how evidence shapes the future of medicine? As Associate Director Evidence Partnerships &amp; Solutions, you’ll be at the forefront of pioneering strategic collaborations and innovative methodologies that drive impactful evidence generation across therapeutic areas. This role offers a unique opportunity to influence global healthcare outcomes by integrating cutting-edge technologies and real-world data into the development of life-changing treatments. Join us in shaping the future of evidence excellence at Novartis. Job Description<h4>Key Responsibilities</h4><ul><li>Drive identification and scaling of strategic partnerships and solutions aligned with business priorities</li><li>Pilot innovative methodologies and digital tools to enhance evidence generation impact and scalability</li><li>Recommend fit-for-purpose data and integrated evidence solutions to support product access and adoption</li><li>Translate evidence generation needs into scalable technology requirements in collaboration with cross-functional teams</li><li>Connect internal and external stakeholders to ensure consistent implementation of advanced solutions</li><li>Promote adoption of novel scientific methods including pragmatic studies and hybrid trial models</li><li>Develop learning content and toolkits to support new evidence capabilities across global teams</li><li>Build and evaluate partnerships with medical societies, academic institutes, and data owners</li><li>Ensure compliance with regulatory and ethical standards in partnership and solution development</li><li>Maintain data quality and integrity across research initiatives in alignment with global best practices</li></ul><h4>Essential Requirements</h4><ul><li>Advanced degree or equivalent education/degree in life science/healthcare required. MBA or equivalent preferred</li><li>Minimum 10 years experience and 5 years’ in pharma, academic research, or healthcare with focus on evidence generation</li><li>Proven expertise in interventional and non-interventional trial design and RWE methodologies</li><li>Strong understanding of global regulatory and access environments</li><li>Excellent communication skills with ability to simplify complex scientific concepts</li><li>Experience working across geographies and navigating global healthcare systems</li></ul><h4>Desirable Requirements</h4><ul><li>Prior experience in strategic partnerships and alliances, including managing external scientific collaborations</li><li>Strong leadership background in international, multidisciplinary drug development or country-level product teams</li></ul> 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>Mid Level

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