We’re looking for a regulatory medical writer,

UK-based only!

Requirements:

• Up to 3 years’ of experience with demonstrable success
• Exceptional scientific and medical writing skills
• Ability to understand and process complex information
• Meticulous attention to detail to deliver quality
• Proficient use of Word, Excel, PowerPoint, Outlook, Adobe
• Proficient use of internet searches including PubMed

• Excellent time management to deliver on time and budget
• Experience in regulatory medical writing an advantage
• Competent and confident liaising with clients
• Able to take feedback, learn, develop, grow, and contribute
• Minimum degree requirement: Bachelor’s

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