Celgene Associate Director, Medical Affairs - Immunology and Inflammation in Stockley Park, United Kingdom
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.
The Associate Director, Medical Affairs will assist in the development of, and conduct a variety of Medical Affairs initiatives. He/she 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.
The successful candidate will be able to interact with a wide group of external opinion leaders and other stakeholders in order to deliver medical affairs initiatives. They will also have the opportunity to manage a small team.
Role and Responsibilities
Act as therapy area expert to provide strategic medical input into the company decisions on specified therapeutic areas as required.
Attends 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.
To lead on key congress activities such as Scientific Reviews or Advisory Boards.
To provide strategic input into the development and execution of clinical trials activities and publication plans.
Provide scientific input & feedback on post marketing study proposals.
To review and approve materials to ensure all claims are substantiated by scientific data and are in accordance with the ABPI/IPHA Codes of Practice.
To work 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 the execution of the medical strategic plan.
To provide leadership and support to other Medical Affairs teams (medical liaison and medical information).
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.
Develop scientific presentations (for example those for RML use, or educational materials).
Develop and review 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.
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 Health Technology Appraisals or other market access submissions as required.
Advise on medical safety or clinical issues as required.
Skills and Knowledge Requirements
Medical degree or registered pharmacist - essential.
Experience of the UK pharmaceutical industry including experience in medical affairs - essential.
Demonstrable understanding of regulatory, pharmacovigilance and clinical development.
MHRA Registered ABPI Code of Practice Signatory - preferred.
Excellent verbal and written communication and organizational skills.
Strong identification with Celgene’s values.
Excellent interpersonal skills.
Good team working skills.
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.
Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.COMMITTED TO IMPROVING THE LIVES OF PATIENTS WORLDWIDE