Job Overview: Data Management leadership on studies and take responsibility for the development of the project documentation, system set-up, data entry and data validation procedures and processes assigned to more junior staff. Assume responsibility for all
Career CategoryClinical Job Description The department of Clinical Pharmacology, Modeling and Simulation (CPMS) within Amgen is dedicated to the development of novel, effective, and safe medicines. We are seeking a highly experienced Senior Associate to join the CPMS
Company – Novo Nordisk Global Business Services (GBS) Department – Clinical Data Science Location – Bangalore, India Drive life-changing innovation through data, where your programming expertise transforms clinical trials into breakthrough therapies for millions. Your new role As
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring
ROLE SUMMARY As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Associate Database Analyst is responsible for the programming of high-quality clinical databases. Responsible for supporting assigned
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Position Summary: The Senior Clinical Data Associate provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating
Clinical Trial Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart
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The Senior Clinical Research Associate I is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and
Use Your Power for Purpose Reporting to the Research & Development division, you will be integral in bridging evidence-based medical decision support with colleagues and stakeholders to enhance health and treatment outcomes. By developing frameworks to
Role Description The Clinical Research Associate - Entry Level role is a full-time, on-site position based in Hyderabad. In this role, the associate supports the planning, setup, and monitoring of clinical trials under the guidance of senior clinical research staff. Day-to-day
About the Role Evervie is building a new specialty care vertical focused on womens health, a ground-up clinical model spanning diagnosis, treatment protocols, and a physician panel. Were hiring a Clinical Associate to sit in the founders office and
Job Title: Clinical Research Associate (CRA)/ Senior Clinical Research Coordinator Company: MS Clinical Research Pvt Ltd Experience: Minimum 3 years About Us MS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We
Role Description The Clinical Data Management Associate (Freshers) role is a full-time position based out of Bengaluru, Hyderabad, or Chennai, providing an opportunity to start a career in clinical data management. In this role, the associate will support clinical data review
Role Description The Clinical Trial Associate – Fresher role is a full-time, on-site position based in Bengaluru. The role involves supporting the clinical operations team in planning, organizing, and tracking clinical trial activities. Day-to-day responsibilities include maintaining and updating the
Career CategorySafety Job Description The Global Safety Therapeutic Areas serve as the safety experts for all Amgen products globally and are accountable for the safety strategy and major safety deliverables for each Amgen product. Leaders in
We are Growing! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization. Biorasi is looking
Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the