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Reference No: J11976

Senior Medical Writer - Available due to growth and internal promotion
Home-based (occasional travel to offices/client meetings)
Salary and Benefits:
£30,000 - £40,000
•20% bonus
•Private healthcare

Company/Role Overview:
My client is a global technical leader in the life sciences industry, and they are actively looking for a passionate and driven individual to join their fast-growing and expanding company as a Senior Medical Writer (within Regulatory Affairs - clinical trial focus). Your position at the company will entail working within a welcoming environment, and one that is driven to expand and deliver constant high-quality expertise to the industry.
A Senior Medical Writer plays a critically important role in executing Outsourcing projects. They work as part of high-performing teams on challenging assignments involving the processing of complex scientific, medical and technical information.
Medical Writing projects will typically involve filtering, cleaning, migration, analysis, reporting and publication of clinical data and information. These activities are undertaken according to defined processes and operating procedures, which will be subject to internal and external audit.

Main Job Responsibilities:
•Writing, editing, and summarising clinical documents (clinical study reports, summaries...)
•Produce external scientific communications/publications
•Developing journal manuscripts and clinical trial-related documents
•Undertake projects independently in defined timelines
•Participating in client meetings as required

Candidate Requirements:
•2-3 years Medical Writing experience
•Relevant scientific degree (the more advanced, the more advantageous)
•Experience of global clinical trials in addition to significant clinical research (or academic) experience
•Excellent ICH-GCP guideline knowledge
•Knowledge of EU Disclosure work, clinical study reports, investigator brochures, and patient safety narratives

This role enables a person with the above values and experience to enter a company who are leading professionals in their industry. The position offers the chance to work across Europe and the UK with world-renowned clients.

If this role appears to suit your ambitions and experience, please contact Ridda at Regulatory Professionals on 0118 952 2797 or via email

This role is available due to internal promotions within our client’s company, if the role is not suitable for you, we are offering an excellent referral bonus of £250 in vouchers for anyone you refer to us who go on to get placed in the role.

Please find the link to the results of our salary survey for 2014: – a complementary hard copy can be ordered from the website.

Key words: Regulatory Affairs Medical Writer Clinical Trials ICH GCP Clinical Documentation Writing Home Based UK Home Working

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