Clinchoice Inc.

Clinchoice Inc.

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

United States · Senior

Sponsorship not specifiedDetected 119 days ago
GCPClinical TrialsFDA RegulatoryCommunicationPublic SpeakingBiostatisticsRegulatory Affairs

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odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Employer immigration record

from this employer's Department of Labor filings

Green-card follow-through: 90%

Of 10 labor certifications old enough to have been used, 1 expired without the employer filing the next step. Median time from filing to decision: 490 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • 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.

Requirements

  • MD, PharmD, PhD, or Master's degree in Life Sciences, Oncology, Pharmacy, or related field.
  • Demonstrated expertise in Oncology, with significant experience in Ovarian Cancer.
  • Familiarity with ICH, GCP, GPP, FDA, EMA, and international regulatory requirements.

Nice to have

  • 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.
  • Clinical study reports (CSRs)
  • Protocols and amendments
  • Investigator brochures

Benefits

  • Medical Writing
  • Develop and review scientific and medical materials, including:
  • Slide decks and educational materials
  • Medical information responses and FAQs
  • Collaborate with cross-functional teams to support regulatory submissions and medical affairs activities.
  • Medical Review

This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.