Senior Medical Document Specialist
17 hours ago
A highly skilled Medical Writer II is required to coordinate, write and edit clinical study documents. The role involves:
- Coordinating, writing and editing of Investigator Brochures (IBs), Clinical Study Protocols (CSP), Participant Information and Consent Forms (PICFs) and other clinical study documents.
- Serving as primary technical contact for clinical study documents assigned.
- Mentoring junior Medical Writers on their tasks and maintaining quality processes.
The ideal candidate will possess strong research report writing skills, knowledge of ICH GCP guidelines, medical terminology and clinical trials processes. They should also have excellent time management and organisational skills, with the ability to work unsupervised and contribute to a positive team culture.
Benefits and CultureThis company offers a supportive and collaborative environment, long term career prospects and flexible working arrangements. As a growing business, they are looking for professionals who share their values to join their team.
The company culture prioritises employee-centric practices, which provides opportunities for growth and development. If you're passionate about medical writing and want to be part of a dynamic team, this could be the perfect opportunity for you.
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