Description
We are seeking a Clinical Document Coordinator to join our team. As a Clinical Document Coordinator, you will be responsible for the preparation and review of clinical documents such as patient safety narratives and clinical study report (CSR) appendices.
Key responsibilities include:
- Preparing and reviewing patient safety narratives
- Providing support to project management of narrative projects
- Compiling CSR appendices
- Preparing lower complexity documents such as synoptic or abbreviated CSRs under the guidance of more senior staff
- Assisting Medical Writers in the preparation and background writing of clinical study protocols, CSRs, and subject narratives
- Ensuring timely delivery of high-quality documents to internal customers and Sponsors
- Maintaining excellent working relationships with all clients, both internal and external
Requirements:
- Minimum of first degree in life sciences (or equivalent)
- Advanced degree (e.g., PhD or Masters) preferred
- 1-2 years of narrative writing experience
- Excellent command of written and spoken English
- Good written and verbal communication skills
- Knowledge of MS Word
- Good organisational and time management ability
- Excellent interpersonal skills
- Scientific or Clinical research experience desirable