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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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Quality Assurance Coordinator

Clario

1 year

July 9, 2026

Online Application

Data Operations Coordinator

IQVIA

July 9, 2026

Online Application

PV Scientist

IQVIA

2–3 years

July 9, 2026

Online Application

Project Coordinator

Clario

1–3 years of pharma or CRO experience

July 8, 2026

Online Application

STEM Content Analyst (Market Access/Managed Care Data/PBM)

Clarivate

Minimum 2 Years

July 8, 2026

Online Application

Quality Assurance Auditor II

Novotech

2 Years

July 8, 2026

Online Application

Analyst – Health Economics & HTA | Analyst – Life Sciences Consulting

IQVIA

0 - 3 Years

July 7, 2026

Online Application

CRA I/II

ICON Plc

3 years

July 7, 2026

Online Application

Centralized Monitoring Analysts

Thermo Fisher Scientific

2 years

July 7, 2026

Online Application

Drug Safety Associate

Freyr Solutions

1 - 4 Years

July 7, 2026

Online Application

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