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Jobs in Frankfurt, Germany

Medical Writer

Translational Research in Oncology

Berlin
Remote
EUR 60,000 - 80,000
26 days ago
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Teamlead (gn) SAP Basis

jungwild GmbH

Germany
Remote
EUR 90,000 - 110,000
26 days ago

Account Executive (German/English) - Remote Germany

Vistaprint

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Remote
EUR 40,000 - 60,000
26 days ago

BEYONDinfluence - Marketing Coordinator

JobRack

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Remote
EUR 40,000 - 60,000
26 days ago

Senior Fraud Specialist

Xsolla

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EUR 40,000 - 60,000
26 days ago
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Senior DevOps / Platform Engineer (m/w/d) – Kubernetes & API-Plattform | 100% Remote

peoplesource GmbH

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EUR 70,000 - 90,000
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puro Personaldienstleistung GmbH

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EUR 44,000 - 52,000
26 days ago

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Akkodis

Sindelfingen
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EUR 50,000 - 70,000
26 days ago
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Medical Writer

TRIO - Translational Research in Oncology

Berlin
Remote
EUR 60,000 - 80,000
26 days ago

Creative Strategist / Copywriter (m/w/d) 100% Remote

4creative

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EUR 60,000 - 90,000
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Munderkingen
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EUR 60,000 - 80,000
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EUR 20,000 - 40,000
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EUR 45,000 - 55,000
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26 days ago

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EUR 52,000 - 85,000
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EUR 40,000 - 55,000
26 days ago

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EUR 30,000 - 45,000
26 days ago

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EUR 55,000 - 80,000
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Medical Writer
Translational Research in Oncology
Remote
EUR 60.000 - 80.000
Full time
26 days ago

Job summary

A global academic clinical research organization is seeking a Medical Writer for its team. This home-based role in Germany involves preparing and finalizing critical trial documents, ensuring compliance with regulations, and collaborating on data analysis. Candidates should have a Bachelor’s degree in a medical field, 3-5 years of medical writing experience, and strong communication skills. The organization offers growth opportunities, flexible hours, and employee support programs.

Benefits

Annual compensation review
30 days paid vacation
Flexible work hours
Monthly internet allowance
Employee Assistance Program

Qualifications

  • 3-5 years of experience as a medical writer.
  • Strong ability to write clear and engaging content.
  • Proven experience managing multiple trials with documentation.

Responsibilities

  • Prepare and finalize trial-related documents.
  • Coordinate document-related meetings.
  • Ensure compliance with regulatory guidelines.
  • Perform quality control checks.
  • Collaborate on data analysis and interpretation.

Skills

Medical writing
Clinical research understanding
Strong communication skills
Collaboration
Proficient in Microsoft Office
Reference management tools

Education

Bachelor’s degree in a medical-related field

Tools

Microsoft Office
Statistical software
Job description

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 paidvacation
  • 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

Prior to applying please review TRIO's Applicant Information Notice

Teamwork · Passion · Integrity · Innovation

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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