Senior medical Regulatory writer - Homebased
A Senior Medical Regulatory writer job position has opened up at an international contract research organisation providing drug discovery, lifecycle management and laboratory services. With offices in over 45 countries and approximately 13,000 professionals, this company provide innovative ideas behind multiple sectors. This position can be home, or office based in UK, Spain or Switzerland. As part of this CRO's on-going growth, they are currently recruiting for a Senior Medical Writer to join their rapidly expanding team of over 90 regulatory writers based in Europe, North American and Asia Pacific. Role Overview:The Phase II-IV Medical Writing group, which is part of the Biostatistics Department, includes Writers who prepare documents in support of clinical trials and who assist Regulatory Affairs professionals with marketing applications, INDs, paediatric investigational plans, clinical trial applications, and other types of regulatory documents. This company's team of writers possess strong leadership and project management skills, are creative problem solvers and decision makers, are engaging mentors and enthusiastic members of the department with an eagerness to continually improve our offerings and deliver a market leading service to our clients. In return, the medical writing department offers a highly competitive compensation package together with excellent opportunities for personal development and progression within the field. All within a friendly, fast paced and exciting environment. The Medical Writer collaborates with internal and sponsor team members to interpret, distil, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarisation of preclinical and clinical studies for preparation of investigator's brochures and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications. Skills and Requirements: * Education to Bachelor’s/advanced degree level in a scientific discipline * Prior experience within regulatory medical writing * Excellent grammatical, editorial and proofreading skills * Effective organisational and planning skills * Motivation, initiative and adaptability * Ability to work effectively in a team * This position can be home, or office based in UK, Spain or Switzerland. To Apply:Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable. In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website - www.proclinical.com. A full job description is available on request. ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.