At Fortrea, we deliver clinical development solutions to pharmaceutical and medical device companies. Our services span across 20+ therapeutic areas, covering over 90 countries worldwide.
About the Role
This leadership position requires a seasoned Medical Writer to develop high-complexity clinical regulatory documents that are pivotal to our partners' projects.
The ideal candidate will possess exceptional communication skills, team leadership abilities, and adaptability in managing complex tasks and processes. They should be comfortable working with various stakeholders and confidently contributing their expertise to project teams.
This job involves using your expertise to write, advise, and coordinate the development of critical documents such as Clinical Study Protocols, Clinical Study Reports, Investigator Brochures, clinical summary modules, and overview documents for regulatory submissions globally.
Key Responsibilities Include:
* Leading authoring and development of high-complexity clinical regulatory documents
* Collaborating with project teams to ensure document alignment with project strategy
* Developing and implementing efficient writing processes and quality control measures
As a key member of our team, you will contribute to shaping the future of drug and device development for our partners and patients worldwide.
We offer comprehensive training and support to help you grow professionally and take on new challenges. Whether you're interested in advancing your medical writing skills or exploring management opportunities, we provide the resources to help you succeed.