Lead the strategic planning, development, and oversight of scientific content across multiple therapeutic areas. Ensure that publications, manuscripts, abstracts, posters, and presentations are scientifically accurate and ethically compliant. Collaborate with internal teams and freelance contributors to guide content creation and ensure timely delivery of high-quality materials.
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- Define the scope of formatting, report publishing, or Clinical Study Reports (CSR) Appendices activities with the document author.
- Coordinate and track activities and perform detailed quality reviews; import and route documents in the regulatory information management systems (RIMS).
- Contribute to the development, implementation, and maintenance of medical writing operations business processes; act as subject matter expert (SME) for the master file system.
This position requires a strong candidate with expertise in the analysis of medical literature, data from clinical trials and pre-clinical studies, and sound knowledge of applicable regulations and standards. The position will mainly focus on the development of Clinical Evaluation Plans (CEPs) & Clinical Evaluation Reports (CERs). The purpose of this job is to collaboratively develop strategies for the creation of CEPs followed by the development of clinical evaluation reports (CERs) per EU MDR, to meet essential requirements in support of submission for CE Mark application to obtain Declaration of Conformity and EU market clearance, re-certification and proposed indication/labeling changes.
This position within Medical Communications is fundamental to building credibility and strengthening relationships with healthcare providers, patients, and industry clients, delivering industry-leading services such as call center staffing and medical writing.
This position is responsible for leading the development and delivery of scientific training programs for the North America Medical Affairs team with a primary focus on diabetes and Abbott Products. The role ensures scientific and operational readiness through structured onboarding, continuous education, and performance coaching. It also supports field deployment during territory vacancies and contributes to cross-functional initiatives aligned with business priorities and compliance standards.
You will create accurate, engaging, well-written referenced scientific content for a variety of life sciences training deliverables (e.g., self-study curricula assets, workshops) and represent the scientific team on assigned projects. The role involves researching material, writing referenced drafts, incorporating instructional design elements, and collaborating with internal team members.
Serving as a key link among essential functions, the Scientific Communications Medical Writer ensures the clear, precise, and accessible communication of critical information. By interpreting clinical study results and collaborating with healthcare professionals and cross-functional teams, the medical writer will prepare journal manuscripts and conference materials to support product development and marketing efforts.
Reporting to the Senior Director, Scientific Communications, the Director, Scientific Communications will drive publication and data dissemination strategy across the lifecycle of an asset, developing and executing a comprehensive publication plan and supporting overall Medical Affairs communication plans, collaborating closely with Clinical Development, Biostatistics, Brand Team, and Medical Affairs to ensure strategic alignment and seamless execution.
This is a field-based role where you'll engage in non-promotional, customer-facing activities, discussing scientific issues regarding Viatris medicines. Responsibilities include KOL relationship management, developing medical education materials, and communicating insights related to company objectives. You will also provide training to internal Viatris functions on products and disease states.
The Scientific Director, Medical Affairs will serve as a TIL cell therapy therapeutic area expert in educational, strategic, and tactical discussions/presentations with internal colleagues as well as external experts and investigators. They will support field clinical activities and lead the development of impactful content for the Field Medical Team. Strong cell therapy expertise and recent clinical experience is required.