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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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Medical Physician, Medical Writer & Regulatory Roles

Fortrea

1 - 3 Years+

July 16, 2025

Online Application

Medical Writer

Remedium

1 - 3 Years

July 15, 2025

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Medical Surveillance Specialist

IQVIA

2 to 6 years

July 15, 2025

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Sr Project Support Team Coordinator

IQVIA

1-3 years

July 15, 2025

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CRA, Medical Writer & QA Manager

Ardent CRO

2 - 6 Years

July 14, 2025

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Safety Associate (Aggregate)

Navitas Life Sciences

1-3 years

July 14, 2025

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Holter Specialist

IQVIA

1+ years

July 14, 2025

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eTMF Specialist

OrciMed Life Sciences

3 years

July 14, 2025

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Junior Medical Writer

Medzen Innovations

0 - 2 Years

July 14, 2025

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Medical Representative (MR)

Group Pharmaceuticals

0 – 6 years

July 13, 2025

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