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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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Health Operations Associates

Accenture

0 - 3 Years

June 27, 2026

Online Application

Safety Associate

IQVIA

1 to 2.5 years

June 26, 2026

Email Application

Global Data Management Professionals

IQVIA

Strong Clinical Data Management expertise.

June 26, 2026

Online Application

Technical Reporting Associate I

Labcorp

0–2 years

June 26, 2026

Online Application

Medical Writing Support Coordinator

Parexel

June 26, 2026

Online Application

Medical Writer

Syneos Health

3–5 years

June 25, 2026

Online Application

Sr Documents Specialist

IQVIA

2–4 years

June 25, 2026

Email Application

Sample Management Specialist

Precision Medicine Group

2 - 3 Years

June 25, 2026

Online Application

Associate Data Scientist

Clario

1 - 3 Years

June 25, 2026

Online Application

Lab Cent Project Coord 1

IQVIA

Freshers / Interns Preferred

June 24, 2026

Online Application

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