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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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Associate Content Analyst – Data Annotation

Clarivate

0 - 2 Years

February 12, 2026

Online Application

Safety Science Analyst

Fortrea

0 - 6 Months

February 12, 2026

Online Application

Document Specialist I

Parexel

3 Years

February 12, 2026

Online Application

Senior Researcher / Associate Analyst

GlobalData

0–1 Year

2.75 – 3.75 LPA

February 11, 2026

Online Application

Scientist – Bioanalytical Lab

Syngene

1–3+ years

February 11, 2026

Online Application

Medical Affairs Intern

Novartis

Freshers

February 11, 2026

Online Application

Safety & Pharmacovigilance Coordinator (CT/Literature)

Syneos Health

1+ year

February 11, 2026

Online Application

Site Solutions & SVR Specialist

IQVIA

2 - 8 Years

February 11, 2026

Online Application

Business Operations Analyst

IQVIA

0 - 1 Years

February 11, 2026

Online Application

Senior Regulatory Document Coordinator

IQVIA

2 - 3 Years+

February 10, 2026

Online Application

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