Senior Medical Writer – Sponsor Dedicated
Syneos Health
full-time
Posted on:
Location Type: Remote
Location: Spain
Visit company websiteExplore more
Job Level
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 including clinical study protocols, reports, and manuscripts
- Adheres to established regulatory standards
- Coordinates quality and editorial reviews
- Acts as peer reviewer for internal team
- Provides feedback to define statistical output requirements
- Mentors and leads less experienced medical writers
Requirements
- 3-5 years of relevant experience in science, technical, or medical writing
- Experience working in the biopharmaceutical, device, or contract research organization industry required
- Strong understanding of FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly required
- Experience writing relevant document types required
- 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
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 reportsmanuscriptsregulatory standardsstatistical output requirementsEnglish grammarAMA Manual of Style
Soft skills
leadershipmentoringcommunicationpeer reviewingfeedback provision