Jobs / United States / Clinchoice INC
Medical Writer / Medical Reviewer Consultant – Oncology (Ovarian Cancer)
Clinchoice INC · 🇺🇸 United States
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 17 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 5 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Clinchoice INC paid sponsored hires in similar roles1 certified filing for “Associate Director, Medical Writing” (Natural Sciences Managers) in NY: $150k–$150k, median $150k. Most were filed at wage level II (100%) — 2 lottery entries, ≈31% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Clinchoice INC
The US Department of Labor certified 17 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 5 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Clinchoice INC →
About the role
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.