Medical Writer / Scientific Writer (Part-Time, Contractor)

Traverse Health is expanding its global research and analytics team, and we’re looking for a part-time Medical Writer / Scientific Writer to support the development of high-quality clinical, scientific, and real-world evidence (RWE) materials across multiple therapeutic areas (cardiometabolic, oncology, autoimmune, neurology, and more).This is a remote B2B contractor role, ideal for someone who excels in scientific communication, clinical documentation, and translating complex data into clear, impactful materials.As a Medical Writer at Traverse Health, you will contribute to the preparation, refinement, and quality control of clinical and scientific documents that support research, evidence generation, and client-facing deliverables. You will work closely with clinicians, data scientists, and project teams to ensure scientific accuracy, regulatory alignment, and clear communication.Approx. 10–20 hours/week, flexible.Key Responsibilities: 1. Scientific & Clinical Document Development• Draft, edit, and refine clinical and scientific documents, including:Study synopses & protocolsStatistical Analysis Plans (SAPs)Clinical study reportsScientific summaries and literature reviews• Ensure consistency, clarity, and alignment with GCP/ICH and scientific standards• Conduct background research and integrate scientific sources into deliverables2. Research Communication & Reporting• Prepare structured reports, progress updates, and evidence summaries• Support the development of materials for ethics submissions and regulatory documentation• Contribute to manuscripts, slide decks, and other scientific communication materials3. Medical Content & Insights Support• Provide scientific input for medical and market access dashboards• Collaborate with data teams to interpret clinical outputs and ensure accuracy• Help communicate research findings to both technical and non-technical audiences4. Cross-Functional Collaboration• Work with internal research teams to translate study requirements into well-structured documentation• Ensure alignment between client expectations and scientific deliverables• Participate in internal calls to provide methodological and scientific insightQualifications: • Degree in Medicine, Pharmacy, Life Sciences, Biomedical Sciences, Public Health, or a related field• Demonstrated experience in medical writing, scientific writing, clinical research documentation, or RWE projects• Strong understanding of clinical research methods, study design, and GCP/ICH guidelines• Exceptional scientific writing, editing, and literature research skills• Ability to translate complex clinical and scientific concepts into clear, structured material• Fluent English (Spanish/Portuguese is a plus)• Ability to work independently in a remote, fast-paced environment