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ClinChoice

Global CRO providing full-service clinical development

Medical Writer / Medical Reviewer Consultant - Oncology, Ovarian Cancer

Technical WritingConfirmed live in the last 24 hours
Full-timeRemote in USANo salary listed

About the Job

Requirements

  • 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

Responsibilities

  • 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
  • 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
  • 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)

Desired 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

About the Company

ClinChoice

Global CRO providing full-service clinical development

ClinChoice is a global contract research organization (CRO) that provides outsourced clinical development services across the full lifecycle for pharmaceutical, biotechnology, medical device, and consumer health customers. It delivers services such as clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance to support trials from early development through post-approval. The company differentiates itself with a large, global workforce—over 4,000 professionals in more than 30 countries—and growth through mergers and acquisitions, enabling multinational trial execution. Its goal is to help clients accelerate approvals and navigate complex regulatory environments by offering flexible project-based and FSP engagement models for end-to-end development and lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Whitemarsh Township, Pennsylvania
Founded
1995

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