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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 Trial Assistant

eAspire Technolabs Inc.

0–1 Year

November 2, 2026

Online Application

Clinical Data Management Associate, Medical Writer, Pharmacovigilance Associate, and Research Associate

eAspire Technolabs

0–2 Years

November 2, 2026

Online Application

Clinical Data Associate

Novotech

6 Months – 2 Year Preferred

November 2, 2026

Online Application

Clinical Data Processor, Specialty Solutions

Clario

0 - 2 Years

November 2, 2026

Online Application

Technical Officer – SAS Programming – CT / SAS Programmer (Late Phase)

Lambda Therapeutic Research Ltd.

1 - 3+ years of SAS programming experience in Pharma/CRO setup

November 1, 2026

Online Application

Clinical Systems Quality Assurance (CQA)

Prime Services CRO (MERIL)

1 Years+

November 1, 2026

Email Application

Analyst, Research Analytics

Inizio Ignite – Putnam

2–5 Years

October 30, 2026

Online Application

Project Associates in Clinical Operations

ICON

1–3 Years

October 30, 2026

Online Application

Clinical Database Designer

Medpace

1 Years+

October 30, 2026

Online Application

Clinical Trial Associate

ICON

Prior experience in clinical research or a strong interest in clinical research

October 30, 2026

Online Application

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