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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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Clinical Data Coordinator

Phastar

2–5 Years

September 8, 2026

Online Application

Clinical Validation Analyst

Icon Plc

2+ Years

September 8, 2026

Online Application

Associate Consultant - Market Research And Analytics

IQVIA

2-5 Years

September 8, 2026

Online Application

Clinical Studies Specialist Coordinator

Medtronic

2 Years+

September 8, 2026

Online Application

Case Specialist for Clinical Trial Cases

ProductLife Group

4 years

September 8, 2026

Online Application

Clin DB Validation

IQVIA

1–2 years of relevant Clinical DB Testing experience

September 7, 2026

Online Application

Primary Market Research Associate Consultant

IQVIA

3-4 Years

September 7, 2026

Online Application

Clinical Data Insights Analyst

Novo Nordisk

2+ years

September 7, 2026

Online Application

Clinical Coordinator I – Ophthalmology; Clinical Project Manager I

Voiant Clinical

1 - 3 Years+

September 4, 2026

Email Application

Senior Specialist Clinical Trial Coordinator

Merck

5–8 years

September 4, 2026

Online Application

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