We are seeking a highly skilled Medical Writer with expertise in clinical research and a solid understanding of preclinical scientific work. The ideal candidate holds a PhD in a biomedical or clinical discipline and brings extensive experience developing scientific, regulatory, and clinical documentation.

In this role, the Medical Writer will work cross-functionally with Medical Affairs and Clinical Success teams, supporting communication across clinical development and translational research. This role is suited to someone who thrives in a detail-oriented but also business focused environment and can translate complex scientific concepts into clear, accurate and engaging written materials.

Key Responsibilities

• Planning, develop, write, and edit scientific and clinical documents, including:

• Clinical study protocols and clinical study reports,

• Investigator brochures

• Regulatory documents (e.g., ethics applications, informed consent forms)

• Manuscripts for peer-reviewed journals

• Scientific summaries, white papers, and conference materials

• Work cross-functionally with Medical Affairs, Clinical, Commercial, and Marketing departments to ensure alignment of clinical messaging, scientific accuracy, and documentation needs.

• Ensure all deliverables meet the highest regulatory and scientific standards.

• Support documentation needs for clinical trials across multiple phases.

• Maintain high-quality standards, ensuring accuracy, clarity, and consistency across all materials.

• Stay current with literature in relevant therapeutic areas, particularly musculoskeletal disorders and translational science.

Required Qualifications

• PhD in biomedical sciences, life sciences, medicine, or a related field.

• Demonstrated experience writing in clinical research (clinical trials, human subject studies, etc.) and regulatory documents.

• Strong understanding of research methodologies and translational frameworks.

• Excellent ability to communicate complex scientific information to varied audiences.

• Excellent ability to collaborate across functions and areas of expertise.

• Exceptional attention to detail with strong editing and project-management skills.

• Familiarity with ICH-GCP, clinical development processes, and regulatory/ethical expectations.

• Fluent in English, Swedish a bonus but not required.

Preferred Qualifications

• Experience in musculoskeletal disorders, orthopaedics, rheumatology, or related fields.

• Background in immunology or mesenchymal stem cell (MSC) research.

• Publication record in peer-reviewed journals.

• Experience in industry, CROs, academic clinical research units, or biotech/medtech organizations.

• Experience preparing documentation for ethics committees or health authorities.

About Cellcolabs

Cellcolabs is a biotech impact startup pioneering the large-scale production of high-quality mesenchymal stem cells (MSCs). With efficient, GMP-compliant manufacturing, we aim to accelerate the adoption of cell therapies worldwide, ultimately improving global health.

Department

Medical Affairs

Locations

Stockholm

Remote status

Hybrid

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