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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

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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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Senior Associate Clinical Outcome Assessment

Parexel

2–3 years

August 12, 2026

Online Application

Project Associate Clinical Portfolio

Syneos Health

1–3 years

August 11, 2026

Online Application

Aggregate Report Writer

COD Research

1 - 6 Years

August 11, 2026

Online Application

Senior Clinical Data Analyst

Parexel

6+ Years

August 11, 2026

Online Application

Associate Clinical Data Coordinator

IQVIA

0 - 1 Years

August 11, 2026

Online Application

Grants Specialist – Clinical Site Payments

ICON plc

0–3 years officially; 6–12 months preferred

3.5–6 LPA

August 10, 2026

Online Application

Clinical Trial Associate

ICON

0 - 2 Years

August 10, 2026

Online Application

Analytics with Japanese Language Specialist, Intern, Primary Market Research Analyst

IQVIA

0 - 5 Years

August 10, 2026

Online Application

EDC Administration Specialist

Regeneron

2+ years

August 10, 2026

Online Application

Production, Packing & IPQA

Aizant Drug Research Solutions

2–5 Years

August 10, 2026

Walk In Interview

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