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New Medical Writing opportunities within a Cambridgeshire based global clinical research organisation have just become available- the result of unprecedented organisational growth. These positions liaising closely both with other internal departments and clients, offer genuine career progression opportunities for any medical writer looking to progress their career. These new positions have the following key responsibilities: ? Independently drafting and revising integrated clinical statistical reports (ICSR) in accordance with SOPs and WPDs: ? Writing and revising clinical trial protocols from detailed outlines provided by the sponsor or internal therapeutic expert. ? Assists in producing regulatory submission documents (CTAs, MAAs, investigator brochures). The successful candidates will have a Life Sciences degree and some medical writing experience preferably gained within a CRO, pharmaceutical or similar clinical research organisation. In addition to excellent medical writing skills, candidates must be able to evaluate and interpret medical research data and be able to follow SOPs and WPDs. Strong communication, organisation and problem solving skills are a pre-requisite as is a strong attention to detail within all aspects of your work. Interested? Send a copy of your CV to mel@squarepegs.biz or call Mel on 0131 473 2343.


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