Medical Affairs Advisor - Haematology

Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease areas such as oncology, cardiovascular, immunoscience and fibrosis. Join us and make a difference. We hire the best people and provide them with a work environment that places a premium on diversity, integrity, collaboration and personal development. Through a culture of inclusion, we create a better, more productive work environment. We believe that the diverse experiences and perspectives of all our employees help to drive innovation and transformative business results. Celgene , a wholly owned subsidiary of Bristol Myers Squibb, is looking for a Medical Affairs Advisor to join the UK Medical team in an interesting and challenging role. 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 or Oncology is desirable + Demonstrable understanding of regulatory, pharmacovigilance and clinical development + Excellent verbal and written communication and organisational skills + Leadership qualities + Compliance with ABPI Code of Practice + Project and time management skills + Adaptability Bristol-Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees the resources to pursue their goals, both at work and in their personal lives. **Company:** Bristol-Myers Squibb **Req Number:** R1522494_EN **Updated:** 2020-05-22 00:00:00.000 UTC **Location:** Hillingdon,United Kingdom Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without reg