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Scientific Affairs Advisor - 12 month fixed term contract United Kingdom,  

Posted on : 27 March 2017

Project Description

Req #: 17000529 Location: Hillingdon, England UK Job Category: Medical 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: Limited Term Job Type: Experienced Job Level: Individual Contributor Travel: No DescriptionCelgene 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.SummaryProvide a comprehensive medical information service to internal and external customers and to support improvements and maintenance of medical information systemsManage out of hours calls and the out of hours service provider contractProvide scientific advisory support for claims / materials development and approval, ensuring compliance with the relevant Code s of Practice and legislationAct as a key member within the cross-functional disease team, working closely with Medical Affairs, Marketing, Market Access and Regulatory, maintaining high levels of Code compliance whilst supporting commercial and medical aims and activitiesRole responsibilitiesProvide scientific advisory support for claims/ materials development, ensuring medical accuracy of scientific content, and compliance with  relevant Code s of Practice and legislation. Responsible for data provision and ensuring data maximises commercial potentialInput into Code of Practice defence of claims from competitor companies, healthcare professions and regulatory authorities as requiredActively involved in the development and implementation of operational plans including disease team and medical plansSupporting Medical Affairs and the Marketing team to develop market leads for developing and driving the disease team plan and leveraging clinical scientific data to optimise the adoption of the promotional campaignsPrepare and deliver brand-related presentations and  training to field teams as requiredAct as a point of escalation for medical information queries  Support and manage the third party service provider including management of contracts, working practices and regular quality control checks to ensure compliance with relevant procedures and legislationFormulate high quality written and telephone responses reflecting the most recently available data on Celgene products in response to enquiries received from both internal and external customers and ensure responses conform to both company guidelines and practices and the ABPI code of practiceDevelop and maintain Medical Information standard responses for use in The UK and Republic of Ireland in collaboration with Global Medical InformationFurther develop and maintain the internal Medical Information databasePerform weekly quality checks (QC) checks on medical information responses, liaising with US colleagues to ensure global consistency and provide reports for all safety enquiries received via Medical Information, to the drug safety team for reconciliationSupport out-of-hours emergency cover in collaboration with Medical Director / Associate Director Medical AffairsEnsure 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 requirementsAttends medical congresses to staff medical affairs booths and acts as an information resource for the company s products. Ensures the disease team are updated on relevant data acquired from medical congressesManage the company s Copyright licences. Liaison with the Copyright Licensing Agency to ensure all clinical papers distributed or received are within copyright laws and our licenceResponsible for the development/maintenance of relevant SOPs, in collaboration with the Medical Director and Associate Director of Quality and Regulatory AffairsQualificationsMedical/Scientific background with a minimum of degree level qualification in pharmacy/pharmacology or relevant biological sciencePast Pharmaceutical Industry experience is desirablePrior experience in the provision of Medical Information service Proven working knowledge of ABPI Code of Practice Past experience in the Inflammation and / or Immunology therapy areas desirableProven skills in:Literature database searching and related computer skillsClinical data interpretationMedical writing skillsCustomer communication skills including a good telephone manner*MONEU


Hillingdon England UK

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