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You will be updated with latest job alerts via emailWe are on a mission to deliver solutions that bring life-changing treatments to patients faster.
But we can´t do it alone. We are seeking a Principal Medical Writer to lead authoring and development of high complexity clinical regulatory documents that are critical to the strategic goals of our partner.
This is why we need you. Join Fortrea. Your job matters.
WHAT YOU WILL DO
This is a full-time, remote job, EMEA.
You will work for one sponsor, imbedded on their team. Under this framework, you will act as an:
Expert Contributor.
You will serve as an expert contributor on our partner’s project teams. You will use your expertise and experience to write, advise, and coordinate development of complex clinical regulatory documents including Clinical Study Protocols, Clinical Study Reports, Investigator Brochures, and clinical summary and overview documents in CTD/eCTD format for regulatory submissions world-wide.
Strategist.
This job is tailor-made for Medical Writers passionate about leading development of key documents that inform and align with project strategy.
Project Manager.
You will be the nexus where multiple teams´ expertise converge. You will leverage your experience to manage writing projects, coordinate and collaborate with stakeholders, steer discussion, drive consensus and facilitate decision-making to propel the document development cycle forward.
YOU NEED TO BRING…
To drive development of documents of this scale forward, this role requires visibility, proactivity, collaboration/teamwork, and excellent communication skills:
Integration within the partner´s team is crucial, requiring readiness to assume augmented responsibilities and adaptability across environments and therapeutic areas.
A UNIQUELY DIVERSE CAREER
At Fortrea, your career path is yours to shape. We empower our team to steer their own development. Where are you in your career journey?
Your aspirations drive your journey with us.
Full Time