Clinical Research Jobs

Location: GBS, Bangalore Shape the future of transformative therapies through rigorous data science and clinical trial excellence. Your new role As a Senior Clinical Data Management Professional, you'

Senior Clinical Python Programmer ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellen

Clinical Nurse Reviewer ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we

Senior CVA, Chennai, Office based ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellen

Centralized Clinical Trial Manager ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excelle

Manager, Clinical Systems ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and

Job Overview Responsible for study design, edit specifications and system configurations. The Clinical database designer is accountable for associated quality and timely delivery of assigned study des

Job Title: Associate Director, Non-Clinical Data and Documents Introduction to role This Associate Director, Non-Clinical Data and Documents role leads a specialist team that underpins high-quality re

Summary Is responsible for executing label design and reviewing related tasks in alignment with label strategy defined by the Label Lead and the established processes. This role ensures t

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted a

Primary Job Function: The Site-ICRA I, based in India, is primarily responsible for support services in partnership and collaboration with the US and EMEA Clinical Site Operations team. Primary focu

Job Description Primary Job Function: The Site-ICRA I, based in India, is primarily responsible for support services in partnership and collaboration with the US and EMEA Clinical Site Operations team

Primary Job Function: The Site-ICRA I, based in India, is primarily responsible for support services in partnership and collaboration with the US and EMEA Clinical Site Operations team. Primary focu

Primary Job Function: The Clinical Contracts Associate (India) will support the US & CALA Clinical Contracts, Budgets & HCP Agreements team, responsible for developing & amending site budgets, initi

Job Description Primary Job Function: The Site-ICRA I, based in India, is primarily responsible for support services in partnership and collaboration with the US and EMEA Clinical Site Operations team

As part of the Clinical Data and Information Sciences (CDIS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Data Manager is responsible for time

The Clinical Evaluation Specialist in the Medical Affairs team plays the lead role in the planning, creation, update of Clinical Evaluation Reports Clinical Benefit-Risk Assessments, Clinical Evaluati

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation

Summary Clinical Trial Supply Manager (CTSM) defines and executes an optimal clinical trial supply strategy for a clinical trial including effective risk management to ensure supply conti

Job Description 1. Provide clinical support and guidance to doctors, nurses, and hospital staff on product usage. 2. Conduct product demonstrations and in-service training at hospitals and healthcare