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Senior Medical Writer – Client Aligned
Thermo Fisher ScientificSenior Medical Writer responsible for developing clinical and regulatory documents for Thermo Fisher Scientific. Collaborating with teams to ensure accuracy and compliance with regulatory guidelines.
About the role
Key responsibilities & impact- Write and edit clinical and regulatory documents
- Collaborate with cross-functional teams
- Ensure documents align with regulatory guidelines and industry best practices
- Review documents prepared by team members
- Manage timelines and deliverables for projects
- Mentor junior medical writers
Requirements
What you’ll need- Bachelor's degree in a scientific discipline or equivalent
- Regulatory writing experience comparable to 5+ years
- Experience in the pharmaceutical/CRO industry
- Experience in managing complex medical writing projects
- EU CTR experience preferred
- Excellent organizational and program management skills.
- Proven leadership skills to manage and mentor a team of medical writers.
- Extensive knowledge of regulatory guidelines and drug development processes.
- Strong interpersonal and communication skills.
- Understanding of quality control processes.
Benefits
Comp & perks- Professional development opportunities
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
Clinical Document WritingRegulatory Document EditingMedical Writing Project ManagementQuality Control ProcessesDrug Development Processes
Soft Skills
Organizational SkillsInterpersonal SkillsCommunication Skills
Certifications
Bachelor's Degree in Scientific Discipline