Responsibilities:
- Writing, editing, and developing regulatory documents such as CSRs, protocols, clinical overviews and summaries, and safety documents, across a range of therapeutic areas
- Medical communications experience advantageous
- Proactively contributing creative ideas, concepts, or suggestions to provide added value to projects
- Liaising with clients, authors and colleagues to progress projects effectively, both remote and on-site
- Developing and continuing relationships with clients to ensure long-term partnerships and collaborations
- Working both independently with minimal supervision and as part of a team
Remuneration:
- Negotiable salary based on experience
- Company and personal performance-related bonuses
- Company pension scheme
- Opportunity for career progression and development
- Fully remote-based role