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Senior Medical Affairs Advisor United Kingdom,  

Posted on : 26 December 2016

Project Description

Req #: 16001677 Location: Hillingdon, England UK Job Category: Clinical Development Work Location: Stockley Park, UK 1 Longwalk Road Stockley Park Hillingdon UB11 1DB Organization: Celgene UK Marketing LTD Schedule: Full-time Shift: Day Job Employee Status: Regular Job Type: Standard Job Level: Individual Contributor Travel: No DescriptionPurpose The Senior Medical Advisor is a critical role within the I&I medical team. This role will be responsible for ensuring the development and delivery of the full range of medical activities undertaken in the UK&Ire Affiliate. This will include the opportunity to line manage the existing medical advisors. The accountability of these activities will remain with the Director of Medical Affairs. This role will be expected to have a strong history and demonstrably successful track record in medical affairs. He/she will be able to demonstrate a deep understanding of the ABPI Code of Practice to ensure accuracy and compliance.   Role and Responsibilities: " Act as therapy area expert to provide strategic medical input into the company decisions on specified therapeutic areas as required. " Develop and maintain strong scientific partnerships with key external experts and professional bodies. " To advise on compliance issues, review and  approve materials  in accordance with the ABPI/IPHA Codes of Practice  and Celgene Standard Operating Procedures (SOP) " Line management of existing medical advisors " Take responsibility for  and manage the  execution of the medical strategic plan " To provide leadership and support to others in the  Medical Affairs teams "  Provide support to the Director, Medical Affairs in developing and implementing Medical Affairs initiatives to support the needs of Celgene UK & Ireland: " Ensuring training of staff to meet technical, medical and interpersonal challenges of their roles " Provide scientific support to Marketing, Regulatory, Market Access, Pharmacovigilance and Risk Management groups " Ensure adverse events and pregnancy reports are duly processed in line with company procedures and assist in assessment of adverse event reports originating in the UK and Ireland for completeness, consistency and reporting requirements " Provide portfolio of data and medical/scientific input to HTA or other market access submissions as required " Advise on medical safety or clinical issues as required QualificationsSkills and Knowledge Requirements: " Registered Medical Doctor " Must be a Final Signatory " Extensive pharmaceutical industry experience including experience in medical affairs- " Demonstrable understanding of the ABPI Code of Practice " Previous line management experience is desirable " Excellent verbal and written communication and organisational skills " Strong identification with Celgene s values " Understanding of pharmaceutical industry " Excellent interpersonal skills " Good team working skills " Leadership qualities " IT aptitude Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.   *LI-KL1 *MONEU 


Hillingdon England UK

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