
Clinical Documentation Specialist
1 day ago
Seeking an experienced regulatory medical writer with advanced writing and editing skills to coordinate, write and edit clinical study documents.
Job DescriptionAs a medical writer, you will be responsible for coordinating, writing and editing Investigator Brochures (IBs), Clinical Study Protocols (CSPs), Participant Information and Consent Forms (PICFs), Clinical Study Reports (CSRs) and other clinical study documents.
Responsibilities- Write and edit high-quality clinical study documents.
- Collaborate with cross-functional teams to develop and implement effective content strategies.
- Advanced degree in a scientific or relevant discipline.
- Minimum 2 years of experience as a medical writer with prior experience in preparation of IBs, CSPs, PICFs, CSRs or other clinical trial documents.
- Strong research report writing skills and/or demonstrated experience in writing peer-reviewed journal articles.
A dynamic work environment with opportunities for career growth and professional development. Collaborative team culture promoting open communication and mutual respect.
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