Regulatory Medical Writing Program Lead

ThermoFisher Scientific

Brussel Hoofdstad

Sur place

EUR 80 000 - 110 000

Plein temps

Il y a 7 jours
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Résumé du poste

Thermo Fisher Scientific is seeking a Program Manager within our Regulatory Medical Writing team in Brussels. You will lead client programs with high visibility, manage relationships, and ensure timely delivery and quality of program documents.

Join a global team that supports top pharma and biotech partners, overseeing budgets, timelines, and processes while mentoring junior writers and driving process improvements.

Qualifications

  • Bachelor's degree in a scientific discipline or equivalent; advanced degree preferred.
  • 8+ years of relevant experience in medical writing/regulated environment.
  • Experience managing and directing complex medical writing projects.
  • Experience in pharmaceutical/CRO industry preferred.
  • AMWA/EMWA or RAC qualifications advantageous.

Responsabilités

  • Develop project timelines, budgets, forecasts and contract modifications for assigned projects; liaises with other departments on changes.
  • Lead client programs and manage relationships to ensure timely delivery and quality of documents.
  • Escalate or resolve risks to project quality, budget, or timeline as needed.
  • Ensure compliance with global/document development guidelines across programs.
  • Provide training for medical writers on processes and program management.
  • Backup medical writer duties including researching and editing complex clinical documents.

Connaissances

Program management
Budgeting
Forecasting
Client engagement
Risk management
Communication
Mentoring

Formation

Bachelor's degree in a scientific discipline
Advanced degree preferred

Description du poste

Thermo Fisher Scientific is seeking a Program Manager within our Regulatory Medical Writing team in Brussels. You will lead client programs with high visibility, manage relationships, and ensure timely delivery and quality of program documents.

Join a global team that supports top pharma and biotech partners, overseeing budgets, timelines, and processes while mentoring junior writers and driving process improvements.

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