FierceBiotech and FiercePharma Jobs
Associate Director Medical Writing-MA - The Cambridge Group LTD
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Website: http://cambridgegroup.com
Position Description
Associate Director Medical Writing
The Associate Director of Medical Writing (ADMW) will focus on the production of high quality publications (eg, manuscripts, abstracts, review articles) and other written communication material (eg, slide presentations, posters) for the company’s Multiple Sclerosis program. Publications and other communication material must conform to high ethical standards for transparency in communicating clinical research results as outlined by GCPs and industry guidelines, as well as the company’s policies and procedures. The AD MW will also collaborate closely with the Medical Affairs department on publication strategy and process. This is an exciting opportunity to be part of a high-profile, high-impact clinical program and to work in a highly dynamic, empowered and collaborative setting. The successful candidate will participate in the development of strategic publication plans and tactics; attend publication planning team meetings. Prepare high quality publications and other written communication material. Manage external resources in the development of publications to meet objectives in a cost-efficient and timely manner, effectively using project management skills. Work closely with lead external authors and assure that their primary responsibility for content adheres to ICJME standards. Liaise with internal and external contributors, including authors and key health care decision makers. Ensure that strategically aligned scientific communication points are delivered and that statements and conclusions are accurate and supported by appropriate data. 3 years previous experience writing and editing peer-reviewed clinical publications (manuscripts, abstracts, posters, oral presentations, review articles, etc.) is required. The incumbent must have been a lead author of at least 8 clinical publications or formal medical writing acknowledgment in at least 8 clinical publications. Solid understanding of manuscript-writing processes for publication in peer-reviewed journals, including familiarity with external clinical publication practices and standards (eg, ICMJE, AMA, CONSORT). Excellent writing and editing skills, including a clear, concise scientific style with attention to detail and the ability to write concise summaries of complex issues. Ability to critically analyze and synthesize complex scientific information from a broad range of scientific disciplines and clinical therapeutic areas. Excellent data interpretation and presentation skills, including some background with biostatistics. Ability to think strategically. Thorough understanding of the clinical drug development process. Demonstrated ability to manage several projects simultaneously. Excellent interpersonal skills, matrix management, negotiation, and leadership skills. Demonstrated ability to make effective decisions even in the absence of complete information and when under pressure. Proficiency in Microsoft Office applications (Word, Excel, PowerPoint) and knowledge of reference and bibliographic software and creation of reference databases are essential. The candidate must have an advanced degree in life sciences along with 6 or more years of pharmaceutical and/or biotech industry experience in publication writing. Experience writing in neurology or multiple sclerosis.
