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

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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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Clin Data Coder 1

IQVIA

2 years

May 16, 2025

Online Application

Centralized Monitoring Assistant

IQVIA

6 Months - 3 Years

May 16, 2025

Online Application

Drug Safety Physicians

ICON Plc

2 - 5 Years

May 15, 2025

Online Application

Operations Specialist 1 - Japanese Linguist (Pharmacovigilance)

IQVIA

1 - 3 Years

May 15, 2025

Online Application

Periodic Report Exp Oversight (PRE)

IQVIA

3-5 years

May 15, 2025

Online Application

Medical Affairs Executive

Wellesta Healthcare

1 - 6 Years

4 - 6 LPA

May 15, 2025

Online Application

Senior Medical Reviewer

Novo Nordisk

1-2 years

May 13, 2025

Online Application

Associate Study Coordinator

Labcorp

2 - 4 Years

May 13, 2025

Online Application

Medical Writer I

Parexel

2–4 years

May 12, 2025

Online Application

Medical Writing, Quality Assurance, Bioanalytical Department

BION Clinicals

Freshers

May 11, 2025

Walk In Interview

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