Senior Medical Writer
2 days ago
A senior medical writer is responsible for creating high-quality regulatory documents for the pharmaceutical and biotechnology industries.
About the PositionThis role involves coordinating, writing, and editing of Investigator Brochures, Clinical Study Protocols, Participant Information and Consent Forms, Clinical Study Reports, and other clinical study documents.
Key Responsibilities- Creation and maintenance of quality processes.
- Mentoring junior writers to ensure consistency in document production.
- Liaison with internal departments and clients to ensure smooth communication.
- Bachelor's degree in a scientific or relevant field.
- Strong research report writing skills and experience in peer-reviewed journal articles.
- Knowledge of ICH GCP, ICH E3 guidelines, medical terminology, and clinical trials processes.
- Excellent time management, organisational, and communication skills.
The ideal candidate will possess strong analytical skills, attention to detail, and the ability to work effectively in a team environment. If you are a motivated individual with a passion for medical writing, we encourage you to apply for this exciting opportunity.
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Senior Medical Writer
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Medical Writer II
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