Principal Medical Writer

October 9

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Fortrea

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Description

• Work for one sponsor, imbedded on their team. • Serve as an expert contributor on partner’s project teams. • Write, advise, and coordinate development of complex clinical regulatory documents. • Lead the development of critical documents that shape and align with project strategy. • Serve as a key liaison, managing writing projects and collaborating with stakeholders.

Requirements

• Advanced degree (PhD or Masters) • Minimum 6 years eCTD submission writing experience, including 3 years as medical writing project lead. • Experience and proficiency in writing and leading development of a variety of clinical regulatory medical writing deliverables. • Proven experience leading stakeholders/project teams through submission document development.

Benefits

• Medical • Dental • Vision • Life • STD/LTD • 401(K) • ESPP • Paid time off (PTO) or Flexible time off (FTO) • Company bonus where applicable.