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Medical Writer (Contractor)

US · Remote · Contract · Others

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About the role

Risk ManagementClinical Research
This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Medical Writer (Contractor) based in the United States. As a Medical Writer, you will contribute to the development and maintenance of high-quality clinical and drug safety documentation supporting pharmaceutical product development and post-marketing surveillance. You will analyze clinical and non-clinical safety data, prepare regulatory reports, and help ensure compliance with global pharmacovigilance requirements. Working alongside drug safety professionals, clinical research teams, and regulatory specialists, you will play an important role in protecting patient safety and supporting informed regulatory decisions. This contract opportunity offers exposure to diverse therapeutic areas and a variety of medical and regulatory documents. You will also contribute scientific expertise to signal assessment, risk management, and safety reporting activities. Ideal for a detail-oriented medical writing professional, this role combines scientific rigor, regulatory knowledge, and cross-functional collaboration in a technology-enabled life sciences environment.