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
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
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
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
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
What we want to accomplish and why we need you Suki is a leading technology company that provides AI voice solutions for healthcare. Its mission is to reimagine the healthcare technology stack, making it invisible and
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
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
Job title : Associate Clinical Data coordinator Experience : 1.5 to 3 years Location : Kochi and Bangalore Mode of work : Office based Job Overview Perform/Assist the Data Manager in managing various data management projects as per
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
Clinical Research Associate (Freshers Only) Location: Remote Organization: Clinogenesis Research Organization Department: Clinical operations Type: Full-Time | Freshers Only About the Role: Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research
Role Overview An entry-level Clinical Research Associate (CRA) to monitor clinical trial sites, verify data quality and ensure GCP compliance and patient safety across assigned studies. Key Responsibilities ■ Support and conduct site visits for study initiation, monitoring and
Role Description The Clinical Documentation Associate - Fresher role is a full-time. The role involves reviewing and organizing clinical documents, ensuring accuracy and completeness of medical records, and maintaining standardized documentation formats. Responsibilities include supporting clinical teams by updating patient
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
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
Clinical Research Associate (Freshers Only) Location: RemoteOrganization: Clinogenesis Research Organization Department: Clinical operationsType: Full-Time About the Role:Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research Associate. Key Responsibilities: Assist with on-site coordination