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
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