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Saturday, November 16, 2013

Senior Medical Writer (Regulatory) - Home based - UK - Employment, career opportunity in UK

Job Title:  Senior Medical Writer (Regulatory) - Home based - UK
Job Type    Permanent
Location    Cambridge
Start Date    ASAP
Salary    Excellent
Ref No    139135-LJ4674-1111


I am currently looking for a high-performance Senior Medical Writer to join our client's dynamic international medical and scientific writing team on a full-time basis.

The company has a strong team of 60+ writers working worldwide, with writers based across the UK, EU and US.

The person suitable for this position will be located in the UK and will either work from home or at our clients HQ based in Cambridge.

The Senior Medical Writer is responsible for researching, preparing, and coordinating scientific publications. The Senior Medical Writer is also responsible for researching, writing, and editing clinical/statistical reports and study protocols, and summarizing data from clinical studies for submission to the Food and Drug Administration (FDA).

When in this position you will need:
*Experience in IND's, NDA's and IMB briefings
*Excellent grammatical, editorial and proofreading skills
*The ability to interpret and present complex data

In this position you will receive;
*Fantastic opportunities for career growth and development
*The opportunity to join a growing CRO with 12,000 professionals and offices in 46 countries worldwide
*Great salary and package

If you have the skills and ambition required please contact Lyndsey Jewitt today by either calling me on +44 (0) 1273 727930 or alternatively send an updated CV to Lyndsey@stelfoxuk.com.

Lyndsey is a Talent Acquisition Consultant for Stelfox UK who specialise in Global Pharmaceutical Recruitment, placing individuals in medical communications positions across the UK, Europe, Asia and South America.

regulatory writing, medical writing, regulatory writer, medical writer, CSRs, protocols, IBs, CTD manuscripts, homebased, home-office, Writing, editing, proofreading, project planning, clinical trials, regulatory submissions, CRO, clinical study protocols, study reports

Stelfox operates on a very simple maxim:
Find out what people want and give it to them.

Please call for details of this or any other opportunities on 01273 727 930



Click to Apply Now



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