Medical Writer

TRIO - Translational Research in Oncology; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A global academic clinical research organization in Germany is seeking an experienced Medical Writer to support the preparation and finalization of clinical trial documents. The role involves managing multiple trials, ensuring compliance with ICH guidelines, and collaborating with internal teams. Candidates should have a relevant degree and 3-5 years of experience in medical writing, along with strong communication skills. This home-based position offers flexibility and various employee benefits including 30 days of vacation.

Leistungen

Annual compensation review

30 days paid vacation

Flexible work hours

Qualifikationen

• 3-5 years of experience as a medical writer, including clinical trial documents.
• Strong ability to write clear, accurate, and engaging medical/scientific content.
• Solid understanding of clinical research concepts, ICH guidelines, and drug development.

Aufgaben

• Prepare, edit, and finalize trial-related documents.
• Coordinate document-related meetings and ensure they meet regulatory guidelines.
• Perform quality control checks and address findings.

Kenntnisse

Clear writing

Communication skills

Collaboration

Ausbildung

Bachelor’s degree in a medical-related field or life sciences

Post-graduate degree preferred

Tools

Microsoft Office

Reference management tools

Jobbeschreibung

Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to bringing the cancer treatments of the future to the patients of today.

TRIO is seeking a Medical Writer to join our Medical Writing and Training team. This position reports to the Medical Writing Manager and is home-based in Germany.

This position is a fixed-term role starting on March 2, 2026, and ending at the end of August 2026.

Responsibilities

• Prepare, edit, and finalize trial-related documents, including:
  • Clinical Trial Protocols and Synopses
  • Clinical Study Reports
  • Patient Narratives
  • Safety Update Reports
  • Abstracts and Manuscripts for publication
• Coordinate document-related meetings, including agendas and minutes.
• Ensure documents meet timelines, regulatory guidelines (ICH), SOPs, and sponsor requirements.
• Perform quality control checks and address findings.
• Maintain and update SOPs and templates for medical writing deliverables.
• Collaborate on data analysis and interpretation to ensure accuracy in documents.
• Submit abstracts, presentations, and manuscripts to conferences or journals.
• Stay current with industry standards and regulatory requirements.
• Suggest process improvements to enhance quality and efficiency.

Qualifications

• Bachelor’s degree in a medical-related field or life sciences (post-graduate degree preferred).
• 3-5 years of experience as a medical writer, including clinical trial documents.
• Strong ability to write clear, accurate, and engaging medical/scientific content for diverse audiences.
• Proven experience managing multiple trials and related documentation.
• Solid understanding of clinical research concepts, ICH guidelines, and drug development processes.
• Familiarity with statistical principles applied to clinical trials.
• Strong communication and collaboration skills with internal and external stakeholders.
• Proficiency in Microsoft Office and reference management tools.
• Native English speaker or highly proficient in English.
• Must be legally authorized to work in the country.

What TRIO Offers

• Annual compensation review and opportunities for growth
• 30 days paid vacation
• 1 volunteer day per year
• Retirement Savings Plan available
• Flexible work hours to promote work-life balance
• Out of country work: employees can request to work internationally for short periods each year
• Monthly internet allowance with a one-time home office allowance
• Employee Assistance Program for you and your family