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Medical Writer – Future Roles
Syneos HealthMedical Writer leading medical writing deliverables in biopharmaceutical organization. Managing activities across studies and ensuring accuracy of scientific documents formatted as per regulatory guidelines.
About the role
Key responsibilities & impact- Leads the clear and accurate completion of medical writing deliverables
- Manages medical writing activities associated with individual studies
- Completes a variety of documents including clinical study protocols, clinical study reports, informed consents, and more
- Adheres to established regulatory standards
- Coordinates quality and editorial reviews
- Acts as peer reviewer for internal team
- Provides technical support, training, and consultation
Requirements
What you’ll need- 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
Comp & perks- health insurance
- career development and progression
- supportive and engaged line management
- technical and therapeutic area training
- peer recognition
- total rewards program
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
medical writingclinical study protocolsclinical study reportsinformed consentsregulatory standardstechnical supporttrainingconsultationFDA regulationsICH regulations
Soft Skills
communicationpeer reviewcoordinationeditorial reviewattention to detailclarity in writingorganizational skillsteam collaborationcritical thinkingproblem-solving