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Medical Writer - Remote
Veröffentlicht am
- Arbeitsort
- Soweto, Deutschland
- Gehaltsschätzung
- 45.000–65.000 € brutto/Jahr · KI-Schätzung von Salary Quick anhand von Jobtitel und Ort (Stand 2026-09-14). Arbeitszeit und individuelle Konditionen können den Betrag verändern. Keine Gehaltszusage.
Stellenbeschreibung
About the Role
Our client is seeking a talented and experienced Medical Writer to join their global team, working entirely remotely. This role is responsible for creating clear, accurate, and scientifically sound documents for a variety of audiences, including regulatory bodies, healthcare professionals, and patients. You will translate complex scientific and clinical data into high-quality written content, ensuring consistency and adherence to relevant guidelines. This is an excellent opportunity for a skilled writer to contribute to impactful medical communications from a remote setting, working collaboratively with cross-functional teams to disseminate critical information about pharmaceutical products.
Key Responsibilities
- Write, edit, and review various medical documents, such as clinical study reports (CSRs), protocols, Investigator's Brochures (IBs), and submission dossiers.
- Develop patient-facing materials, including summaries of clinical trial results and educational content.
- Ensure all medical documentation is scientifically accurate, compliant with regulatory requirements, and meets internal quality standards.
- Collaborate with subject matter experts (SMEs) including clinicians, scientists, and regulatory specialists.
- Manage multiple writing projects simultaneously, adhering to strict deadlines.
- Stay updated on industry best practices and regulatory guidelines for medical writing.
Requirements
- Advanced degree (e.g., Master's, PhD) in a life science, medical, or related field.
- Minimum of 5 years of experience as a Medical Writer in the pharmaceutical or biotechnology industry.
- Proven ability to write clear, concise, and scientifically accurate documents.
- Thorough understanding of clinical trial processes and regulatory submission requirements.
- Excellent command of English grammar, style, and scientific terminology.
- Strong organizational skills and ability to manage projects independently in a remote setting.
Benefits
- Competitive annual salary based on experience and qualifications.
- Fully remote work opportunity, providing ultimate flexibility.
- Comprehensive medical, dental, and vision insurance coverage.
- Generous paid time off and professional development allowances.
- Opportunity to work on diverse and critical medical communication projects.