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Senior Medical Writer, Early Phase

Laboratory Corporation of America Holdings (Covance)

Leeds, United Kingdom

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Covance by Labcorp are seeking an accomplished Medical Writer to join our Clinical Pharmacology Services team in the Early Phase division. This is a full time and permanent, office-based position in Leeds or home-based anywhere in the U.K. The Lead Writer is independently responsible for the preparation of clinical study protocols, clinical study reports (CSRs) and other documents as needed for lower complexity studies. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><strong><span style="color: black;">Your duties will include but not be restricted to:</span></strong></span></p><ul><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Write and coordinate the development of protocols, CSRs or other clinical documents including those of a more complex nature.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Provide support in development of submission level documents under guidance of senior staff.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Oversees management and coordination of complex narrative projects.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Produces scientific papers, abstracts and/or posters, and presentations.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Responsible for all medical writing aspects of project development and coordination, adherence to timelines and budget.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">To prioritize and plan workload to a high standard. Effectively manage multiple assignments in parallel.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Prepare documents in accordance with Covance/Client Standard Operating Procedures and specifications as applicable, and relevant ICH and regulatory/industry guidelines.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Review of Statistical Analysis Plan (SAP) and Tables, Figures and Listings (TFLs) to ensure appropriate data presentation for CSR purposes. Provide feedback on SAP and TFLs to project team as needed.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Act as medical writing contact for major clients and partners.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Keep up to date with developments in Medical Writing.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">In consultation with more experienced staff, show initiative and ability to deal with complex project situations.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Inform management of medical writing problems promptly and propose solutions.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Provide advice on Medical Writing issues to project team members (internal and external) and help to resolve problems.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Contribute to Medical Writing initiatives to develop and improve processes.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Mentor and provide guidance and training to other medical writing staff.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Provide peer review and input on deliverables prepared by colleagues.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Provides scientific leadership and support to colleagues in the data management and reporting team.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Provide support for Business Development opportunities such as time and cost estimates, attendance at client bid defense meetings, industry conferences.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Review Covance SOPs and associated documents.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Represent department in audits and inter-department working groups.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Comply with Covance internal processes and procedures.</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;">Get ready to redefine what’s possible and discover your extraordinary potential at Covance by Labcorp. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 10pt; color: black; font-family: arial, helvetica, sans-serif;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Join us and see why Covance by Labcorp has been named by Forbes as one of the World's Best Employers 2020 and more than 90% of the top 20 global pharmaceutical companies are repeat customers. We can offer you not only a job, but a stable, long-term international career.</span></span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Minimum of first degree in life sciences (or equivalent); advanced degree (e.g., PhD or Masters) preferred.</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Recent and significant medical writing experience including two years as medical writing project lead.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Excellent command of written and spoken English.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Excellent written and verbal communication skills.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">In-depth knowledge of MS Word.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Excellent organizational and time management ability.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Detailed knowledge of ICH guidelines applicable to medical writing.</span></li><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Good understanding of medical/scientific terminology and experience in data analysis and interpretation.</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"><span style="color: black;">#LI-SP2, #LI-REMOTE</span></span></p><p style="margin: 0px;"> </p>

Job posted: 2021-05-25

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