Medical Affairs Advisor Haematology

Celgene ,
London, Greater London

Overview

Req : 1900996 Location: Hillingdon, United Kingdom Job Category: Medical Work Location: 1 Longwalk Road UB11 1DB Organization: Medical Operations Employee Status: Full-time Job Type: Regular Celgene , a wholly owned subsidiary of Bristol-Myers Squibb, is a global biopharmaceutical company committed to changing the course of human health through bold pursuits in science, life-enhancing therapies, and a promise to always put patients first. At the core of that mission are the talented individuals who contribute their unique skill sets to help us drive innovation and deliver truly life-changing drugs for our patients. As we continue to pursue that mission, we're looking for talented professionals like you to join our team. What unique gene will you bring to Celgene? In the Medical Affairs team, you will deliver our mission by assisting in the development of, and conduct a variety of Medical Affairs initiatives. You will also provide technical/scientific consultation to both the medical and the commercial team to ensure accuracy and compliance with the Celgene standard and local rules and regulations. You will have a high level of therapy area expertise and will develop a network of external opinion leaders and other stakeholders in order to develop and deliver medical affairs initiatives. In the Medical Affairs Advisor role, you will support this goal by: Acting as therapy area expert to provide strategic medical input into the company decisions on specified therapeutic areas as required Attending scientific congresses and meetings to maintain therapy area knowledge and to develop/maintain relationships with external customers and influential bodies on behalf of Celgene as required Leading on key congress activities such as Scientific Reviews or Advisory Boards Providing strategic input into the development and execution of clinical trials activities and publication plans Provide scientific input & feedback on IIT proposals Advising on compliance issues, review andapprove materials to ensure all claims are substantiable by scientific data and are in accordance with the ABPI/IPHA Codes of Practice (for example those materials and arrangements related to advisory boards) Working collaboratively within the brand team to provide strategic medical and scientific input into brand plans to develop an appropriate product strategy Take responsibility for and manage theexecution of the medical strategic plan Providing leadership and support to other Medical Affairs teams (medical liaison and medical information) Providing 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 Developing scientific presentations (for example those for RML use, or educational materials) Developing and reviewing training documents to check medical accuracy and compliance with regulatory requirements in order to deliver training to medical and commercial colleagues on such matters as therapy area awareness,competitor data, congress updates etc. Provide scientific support to Marketing, Regulatory, Market Access, Pharmacovigilance and Risk Management groups Ensuring 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 Providing portfolio of data and medical/scientific input to HTA or other market access submissions as required Advising on medical safety or clinical issues as required Skills and Knowledge Requirements: UK registered Medical doctor or Pharmacist (essential due to ABPI Code requirements for signatories) Prior experience as Final Medical Signatory or well underway to becoming a Final Medical Signatory Extensive pharmaceutical industry experience including experience in medical affairs Previous experience in Haematology/Oncology is desirable Demonstrable understanding of regulatory, pharmacovigilance and clinical development Excellent verbal and written communication and organisational skills Strong identification with Celgene's values Leadership qualities Compliance with ABPI Code of Practice Project and time management skills Adaptability About Us COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients. Our vision as a company is to build a major global biopharmaceutical corporation while focusing on the discovery, the development, and the commercialization of products for the treatment of cancer and other severe, immune, inflammatory conditions. "At Celgene, we seek to deliver truly innovative and life-changing drugs for our patients." There are more than 300 clinical trials at major medical centers using compounds from Celgene. Investigational compounds are being studied for patients with incurable hematological and solid tumor cancers, including multiple myeloma, myelodysplastic syndromes, chronic lymphocytic leukemia (CLL), non-Hodgkin's lymphoma (NHL), triple-negative breast cancer and pancreatic cancer. As committed as we are to clinical accomplishment, we are equally committed to patient support, which is a guiding principle at Celgene. We believe all who can benefit from our discoveries should have the opportunity to do so. Celgene puts patients first with industry-leading programs that provide information, support and access to our innovative therapies.