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SENIOR REGULATORY MEDICAL WRITER

5066

My clients a successful medical communications agency with an exceptional track record of delivering to global Partners in pharma, biotech & medical device companies.

" 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

" 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

" Negotiable salary based on experience " Company and personal performance-related bonuses " Company pension scheme " Opportunity for career progression and development " Fully remote-based role

Fully remote homebased

There are no specialist Health & Safety issues related to this role.

Permanent (unless otherwise stated in the job title above).

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To apply for this position you must be eligible to live and work in the UK. Wynne Consulting Limited acts as an Employment Agency as defined by the Conduct of Employment Agencies and Employment Businesses Regulations 2003.

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