Medical Writer / Medical Reviewer Consultant – Oncology (Ovarian Cancer)

New

ClinChoicePharmaceuticals / Biotech

United StatesContractMiddle

Salary not disclosed

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Job Details

Experience: 3–8+ years

Requirements

MD, PharmD, PhD, or Master's degree in Life Sciences, Oncology, Pharmacy, or related field.
3–8+ years of medical writing or medical review experience in pharmaceutical, biotech, CRO, or medical communications environments.
Demonstrated expertise in Oncology, specifically Ovarian Cancer.
Familiarity with ICH, GCP, GPP, FDA, EMA, and international regulatory requirements.
Knowledge of epithelial ovarian cancer, BRCA and HRD biomarkers, PARP inhibitors, and immuno-oncology.
Ability to interpret clinical trial data and publication practices.
Experience with NCCN, ESMO, and ASCO treatment guidelines.
Preferred: Experience with EndNote, PubMed, and Veeva Vault.

Responsibilities

Develop and review clinical study reports (CSRs), protocols, manuscripts, abstracts, posters, and educational materials.
Summarize and interpret clinical data related to ovarian cancer therapies and biomarkers.
Perform scientific and medical review of promotional and non-promotional materials to ensure accuracy and compliance.
Support MLR (Medical-Legal-Regulatory) review processes.
Conduct literature reviews and evidence synthesis from peer-reviewed journals and congress proceedings.
Collaborate with Medical Affairs, Clinical Development, Regulatory Affairs, and Biostatistics teams.

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