Celgene Manager, Medical Affairs in Zurich, Switzerland
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 Manager Medical Affairs is part of the Medical Team and provides a bridge between clinical research and the commercial organization. This position provides operational and scientifically input to the professional functions, and also manages communication-, scientific and/or medical education projects in alignment with the agreed European & Swiss strategy. Opportunity to shape the future of the upcoming I&I Franchise in close collaboration with the commercial local I&I lead.
Responsibilities will include, but are not limited to, the following:
Provide proactive input in the strategic medical and marketing management
Share knowledge and technical expertise with other team members
Develop and implement strategic direction within key therapeutic areas
Develop effective relationships with key influencers and external organizations
Collaboration in cross-functional teams and in formulating and implementing medical strategy
Develop and design of medical information materials and presentations
Answer medical questions on products
Provide training to field representatives and other internal staff
Evaluate and profile potential investigators/sites to participate in clinical development studies and supervise the performance and progress of clinical trials
Initiate, coordinate and provide clinical protocol expertise to physician investigators by collaborating, reviewing, evaluating and assisting with the development, implementation and publication of Investigator Initiated Trials (IITs).
Participates and collaborates with international Medical Affairs team
Lead planning, execution and reporting of key medical projects (e.g, Advisory Boards, communication events, Satellite Symposia, etc)
Support the Regulatory team and Access team with scientific advice as needed in their communications with stakeholders on regulatory and reimbursement matters for Celgene products at any registration stage and indication
Medical degree, Masters Degree or PhD in Pharmacy, Biology or in other relevant scientific fields
Minimum 2 years business experience required in the biotech- and/or pharmaceutical industry, preferable in the Swiss market
Preference given to persons with experience in the Dermatology and/or Rheumatology field
Understanding of commercialization process and clinical development. Knowledge of molecular biology, immunology and pharmacology;
Excellent communication and project management skills
Excellent skills in interacting with internal and external stakeholders
Strong computer skills required, specifically Windows software, including Word, Excel and PowerPoint and Outlook
Fluent written and spoken German, English, French
Strong identification with Celgene’s values
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