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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 & Safety

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

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Bioinformatics Biostatistics Data Science & Analytics Clinical SAS Programming HEOR & Real-World Evidence Medical Writing Scientific Writing Medical Science Liaison

Manufacturing & Quality

Quality Assurance (QA)Quality Control (QC)Pharmaceutical Production R&D & Formulation Pharmaceutical Microbiology Pharmaceutical Packaging Pharmaceutical Warehouse Pharmaceutical Engineering Environmental Health & Safety Effluent Treatment Plant (ETP)Technology Transfer (TDS)

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Regulatory Operations – Regulatory Data Management

Alcon

2–5 years

September 21, 2026

Online Application

TMF Document Coordinator I

Indero

Entry level

September 21, 2026

Online Application

Senior Scientific Writer

Indegene

2–5 Years

7–15 LPA

September 21, 2026

Online Application

Analyst Data QC & Data Processing & Global Data Management

IQVIA

2 - 8 Years

September 21, 2026

Online Application

Drug Safety Analyst

Springer Nature

3 - 5 Years

September 21, 2026

Online Application

Medical Science Liaison Oncology

Johnson & Johnson

0 - 2 Years

September 18, 2026

Online Application

Data Management Associates

Labcorp

2 Years+

September 17, 2026

Online Application

TMF Specialist

ICON plc

2+ years

September 17, 2026

Online Application

Assistant Quality Manager – Clinical Laboratory Services, Medical Writing Team, Biostatistician, and Executive – Purchase & Procurement

Spinos Life Science

0 - 5 Years

September 17, 2026

Email Application

Associate Medical Writing

Eli lilly

experience in technical/regulatory scientific writing.

September 17, 2026

Online Application

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