(Remote â U.S., Central or Pacific Time Zones)
đ§žÂ About the Role
Thermo Fisher Scientific (via PPD clinical research services) is expanding its Medical Writing FSP Team. As a remote Senior Medical Writer, youâll serve as the key author on a variety of regulatory documentsâfrom study protocols to clinical study reportsâensuring accuracy, compliance, and clarity. Youâll play a vital role in supporting clinical research efforts in infectious diseases, oncology, and beyond, contributing to therapies that improve health outcomes globally.
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 Position Highlights
⢠Full-time, fully remote
⢠Schedule: Standard (MondayâFriday)
⢠Location: U.S. Central or Pacific time zones preferred
⢠Competitive compensation + extensive benefits
⢠Mission-driven: Help bring life-changing therapies to market faster
⢠Category: Clinical Research
đ What Youâll Own
⢠Write and revise clinical and regulatory documents (CSRs, IBs, INDs, protocols, MAAs, etc.)
⢠Serve as lead author on routine to complex projects, including summary data interpretation
⢠Collaborate with cross-functional teams, sponsors, and stakeholders
⢠Mentor junior writers and review their work
⢠Ensure compliance with quality standards and global regulatory guidelines
⢠Participate in program-level planning, including timelines, budgets, and contracts
⢠Contribute to client-specific best practices and documentation strategies
đŻÂ Must-Have Traits
⢠Bachelorâs degree in life sciences or related field (advanced degree preferred)
⢠5+ years of relevant experience (pharma/CRO industry strongly preferred)
⢠Solid grasp of global regulatory guidelines and clinical trial processes
⢠Strong command of medical writing, grammar, and editing
⢠Familiarity with document management systems, client templates, and tools like Excel
⢠AMWA, EMWA, or RAC certifications are a plus
⢠Ability to work independently with cross-functional teams and mentor others
⢠Experience in a client-dedicated or multi-project FSP role is ideal
đťÂ Remote Requirements
⢠Must be based in the United States (Central or Pacific time zones preferred)
⢠Must be able to work standard business hours
⢠Reliable internet and home office setup required
đĄÂ Why Itâs a Win for Remote Job Seekers
Youâll join a mission-driven CRO thatâs as focused on employee growth as it is on scientific progress. With award-winning L&D programs, meaningful projects, a flexible work culture, and global collaboration, you wonât just contribute to the future of medicineâyouâll grow alongside it.
đ Perks & Benefits
⢠Competitive salary
⢠Comprehensive health, dental, vision, and life insurance
⢠Generous PTO and paid holidays
⢠Tuition reimbursement + paid certifications
⢠Career advancement pathways
⢠Flexible work environment
⢠Award-winning culture (collaboration, well-being, innovation)
âď¸Â Call to Action
Ready to write the next chapter in medical innovation? Apply now and help accelerate breakthroughs that matter.