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

United States full time

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Remote

senior

H1B: yes

Clinchoice Medical Writer / Medical Reviewer Consultant at Clinchoice specializes in ovarian cancer oncology. The role develops and reviews scientific and medical content ensuring compliance and scientific accuracy.

Responsibilities

Medical Writer / Medical Reviewer – Oncology (Ovarian Cancer)
Position Summary
We are seeking an experienced Medical Writer or Medical Reviewer with expertise in Ovarian Cancer and Gynecologic Oncology to support the development, review, and delivery of high-quality scientific and medical content. The successful candidate will collaborate with Medical Affairs, Clinical Development, Regulatory Affairs, Biostatistics, and external experts to ensure scientific accuracy, compliance, and timely execution of deliverables. The role requires a strong understanding of ovarian cancer biology, treatment landscape, clinical trial data, and publication practices.
Develop and review scientific and medical materials, including:
Clinical study reports (CSRs)
Protocols and amendments
Investigator brochures
Manuscripts, abstracts, and posters
Slide decks and educational materials
Medical information responses and FAQs
Congress presentations and publication plans
Summarize and interpret clinical data related to ovarian cancer therapies and biomarkers.

Qualification

MDAdvanced degree preferredDemonstrated expertise in OncologyExperience with clinical developmentFamiliarity with ICHPublication experience (manuscriptsFamiliarity with EndNote

Required

MD, PharmD, PhD, or Master's degree in Life Sciences, Oncology, Pharmacy, or related field.
Advanced degree preferred.
3–8+ years of medical writing or medical review experience in pharmaceutical, biotechnology, CRO, or medical communications environments.
Demonstrated expertise in Oncology, with significant experience in Ovarian Cancer.
Experience with clinical development, publications, and medical affairs deliverables.
Familiarity with ICH, GCP, GPP, FDA, EMA, and international regulatory requirements.