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Clinical Research Clinical Data Management (CDM)Pharmacovigilance Medical Writing Trial Master File (TMF)Medical Coding SAS Data Sciences Medical Science Liaison (MSL)Medical Reviewer RWE / HEOR

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Clinical Research Clinical Data Management Pharmacovigilance Trial Master File (TMF)Regulatory Affairs Medical Reviewer Medical Coding Pharmacist Medical Devices

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CRA, Bioanalytical, Vendor Qualification, Project Management, Regulatory Affairs (EU, US), MICC, Medical reviewers, ICSR, Aggregate Reporting

Pharmazone

2 - 6 Years

July 7, 2026

Online Application

Complaint Handling Investigator

Philips

2–3 Years

July 7, 2026

Online Application

Safety Writer

Fortrea

2 - 3 Year+

July 7, 2026

Online Application

Associate Scientist Quality Control-Bioanalytical

QPS Bioserve

0–5 Years

July 7, 2026

Walk In Interview

Medical Writer

Indian Immunologicals (IIL)

2–5 Years

July 6, 2026

Online Application

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Roche

Freshers - 1 Years

July 6, 2026

Online Application

Medical Science Liaison (MSL) | Medical Affairs

Bayer

July 6, 2026

Online Application

Business Analyst

Advarra

0–3 Years

July 6, 2026

Online Application

Medical Writer

Imaging Endpoints

1+ Years (Medical Writer), 3+ Years (Senior Medical Writer)

July 4, 2026

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Safety & PV Submission Specialist I

Syneos Health

2 years

July 3, 2026

Online Application

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