Medical Writer, EU
Syneos Health
full-time
Posted on:
Location Type: Remote
Location: Remote • 🇩🇪 Germany
Visit company websiteJob Level
Mid-LevelSenior
About the role
- Leads the clear and accurate completion of medical writing deliverables
- Manages medical writing activities associated with individual studies
- Completes a variety of documents that may include clinical study protocols and clinical study reports
- Adheres to established regulatory standards
- Coordinates quality and editorial reviews
- Reviews documents as needed
- Acts as peer reviewer for internal team documents
- Provides technical support, training, and consultation to department and other company staff
- Mentors and leads less experienced medical writers on complex projects
Requirements
- 3-5 years of relevant experience in science, technical, or medical writing
- Experience working in the biopharmaceutical, device, or contract research organization industry
- Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices
- Experience writing relevant document types
- Extensive knowledge of English grammar and ability to communicate clearly; strong familiarity with AMA Manual of Style
Benefits
- career development and progression
- supportive and engaged line management
- technical and therapeutic area training
- peer recognition and total rewards program
- Total Self culture where you can authentically be yourself
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
medical writingclinical study protocolsclinical study reportsregulatory standardstechnical supportmentoringpeer reviewingEnglish grammarAMA Manual of Style
Soft skills
communicationleadershipmentoringorganizational skills