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

Role overview

Qualifications

  • 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, biotechnology, CRO, or medical communications environments
  • Demonstrated expertise in Oncology, with significant experience in Ovarian Cancer
  • Familiarity with ICH, GCP, GPP, FDA, EMA, and international regulatory requirements

Responsibilities

  • Develop and review scientific and medical materials, including clinical study reports, protocols, investigator brochures, manuscripts, 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
  • Provide expert input regarding ovarian cancer treatment guidelines and emerging therapies

About the company

ClinChoice logo

ClinChoice

Contract Research Organizations (CRO)

ClinChoice is a full-service global clinical CRO dedicated to offering high-quality, efficient and flexible solutions to pharmaceutical, biotechnology, medical device, and consumer products clients worldwide. With a 25 year history of success, ClinChoice continues to be The Standard of Excellence for biostatistics, clinical operations, data management, statistical programming, CDISC, regulatory affairs, medical affairs and pharmacovigilance. ClinChoice has established major delivery centers across US, China, Europe, Canada, India, Japan and the Philippines. It has over 4,000 employees globally, with a strong and talented team, and a growing clinical operations presence in seven countries across Asia, North America and Europe.

Company details

Company typeLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

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Job description

Job Description – Medical Writer / Medical Reviewer (Ovarian Cancer Oncology Expertise)

Position Title

Medical Writer / Medical Reviewer – Oncology (Ovarian Cancer)

Location

Remote / Hybrid

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.

Key Responsibilities

Medical Writing

  • 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.
  • Ensure consistency with ICH, GCP, GPP, and company standards.
  • Conduct literature reviews and evidence synthesis from peer-reviewed journals and congress proceedings.
  • Collaborate with cross-functional teams to support regulatory submissions and medical affairs activities.

Medical Review

  • Perform scientific and medical review of promotional and non-promotional materials.
  • Verify scientific accuracy, consistency, and compliance with regulatory requirements.
  • Review clinical data, references, and claims for accuracy and balance.
  • Support MLR (Medical-Legal-Regulatory) review processes.
  • Provide expert input regarding ovarian cancer treatment guidelines and emerging therapies.

Scientific Expertise

  • Maintain current knowledge of:
    • Epithelial ovarian cancer
    • Platinum-sensitive and platinum-resistant disease
    • BRCA and HRD biomarkers
    • PARP inhibitors
    • Antibody-drug conjugates
    • Immuno-oncology approaches
    • NCCN, ESMO, and ASCO treatment guidelines
  • Monitor publications, clinical trials, and congress updates (ASCO, ESGO, SGO, ESMO).

Required Qualifications

Education

  • MD, PharmD, PhD, or Master's degree in Life Sciences, Oncology, Pharmacy, or related field.
  • Advanced degree preferred.

Experience

  • 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.

Preferred Qualifications

  • Experience supporting ovarian cancer assets or clinical trials.
  • Knowledge of biomarker-driven therapies and companion diagnostics.
  • Publication experience (manuscripts, abstracts, posters).
  • Experience participating in MLR review processes.
  • Familiarity with EndNote, PubMed, Veeva Vault, and reference management tools.

 

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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