Medical Writing Program Manager - Qc And Publishing Lead (fsp)

Thermo Fisher Scientific UK

Competitive salary; not specified; extensive benef...
8+ years experience in medical writing
Experience with csr protocol icf ib documents
Strong project management and resource allocation skills
The role serves as the primary point of contact for clients, ensuring high satisfaction while managing complex document review activities

Job Summary

  • The role serves as the primary point of contact for clients, ensuring high satisfaction while managing complex document review activities.
  • Candidates must have extensive experience reviewing regulatory submission documents such as CSRs, Protocols, and Informed Consent Forms.
  • Thermo Fisher Scientific offers an award-winning learning program, competitive salary, and a flexible working culture focused on work-life balance.

Matching Summary

The role serves as the primary point of contact for clients, ensuring high satisfaction while managing complex document review activities.

Salary

Competitive salary; Not specified; Extensive benefits package including health and well-being focus

Skills & Requirements

Must-have

  • 8+ years experience in medical writing
  • Experience with CSR Protocol ICF IB documents
  • Strong project management and resource allocation skills
  • Excellent oral and written communication abilities
  • Knowledge of global document development guidelines

Nice-to-have

  • AMWA or EMWA certification advantageous
  • RAC certification preferred
  • Experience mentoring entry-level staff
  • Ability to work under pressure meeting tight deadlines
  • Background in pharmaceutical or CRO industry

Key Requirements

  • Bachelor's degree in scientific discipline required
  • Advanced degree preferred
  • 8+ years of relevant experience
  • Medical writing or document review background mandatory
  • Regulatory submission document expertise required

Work Rights

Not specified

Tailored Resume

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