Freelance Medical Writer (QC Specialist)

About Zoe MedCare Zoe MedCare is a specialized medical and regulatory writing agency providing high-quality scientific, regulatory, and medical communication services to pharmaceutical, biotechnology, and healthcare organizations worldwide. We are expanding our network of experienced freelance medical writers to support quality control (QC) activities for Clinical Study Reports (CSRs) and scientific manuscripts. Position Overview We are seeking a detail-oriented and experienced Freelance Medical Writer with strong expertise in Quality Control (QC) of Clinical Study Reports (CSRs) and scientific manuscripts.

The ideal candidate will be responsible for ensuring the accuracy, consistency, completeness, and regulatory compliance of documents prior to client submission. Key Responsibilities Perform comprehensive QC reviews of Clinical Study Reports (CSRs) in accordance with ICH E3 and sponsor-specific requirements. Review scientific manuscripts for accuracy, consistency, grammar, style, and scientific integrity.

Verify data consistency across text, tables, figures, listings, and appendices. Ensure appropriate cross-referencing, citations, numbering, and formatting throughout documents. Identify discrepancies between source data and document content.

Review documents for compliance with applicable regulatory guidelines and publication standards. Provide clear and actionable comments to authors and project teams. Ensure high-quality deliverables within agreed timelines.

Qualifications Advanced degree in Life Sciences, Pharmacy, Medicine, Biotechnology, or a related field (PharmD, PhD, MD, MSc preferred). Minimum 3 years of experience in medical writing, regulatory writing, or document QC. Strong experience reviewing Clinical Study Reports (CSRs).

Experience reviewing scientific manuscripts intended for peer-reviewed journals. Excellent English language, grammar, and editing skills. Strong attention to detail and ability to identify inconsistencies.

Preferred Familiarity with ICH E3, GCP, CONSORT, and publication guidelines. Experience working with pharmaceutical, biotechnology, or CRO clients. Knowledge of statistical outputs, tables, figures, and listings (TFLs).

Experience with oncology, rare diseases, or other therapeutic areas is a plus. What We Offer Opportunity to work on diverse regulatory and publication projects. Competitive hourly/project-based compensation.

Long-term collaboration opportunities for high-performing freelancers. Collaborate with a team of experienced and passionate professionals. Enjoy the freedom and flexibility of freelance, remote work.

Ready to Get Started? You may send your CV to [email protected] We look forward to connecting with you!