Manager US Medical Affairs

Profile

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.

POSITION SUMMARY:

The Manager role will coordinate and provide scientific/medical leadership and support for compounds in various stages of clinical development, as well as approved products in that therapeutic area. This individual will support the design and implementation of a strategic disease area medical plan, under the direction of the Director and in coordination with the US Franchise Team. They will serve as the Biology/Pathway disease expert. They will also support the execution of Celgene sponsored medical affairs trials (as needed) and registries and will also assist in the evaluation and support of investigator-initiated trials. The role will report to the Director/US Disease Lead (Multiple Myeloma). He/she will be headquarters based.

Responsibilities will include, but are not limited to, the following:

Collaborate with Medical Affairs colleagues to guide and execute therapeutic area strategy and tactics with appropriate use of resources. Assist Director on behalf of the Disease Lead as a therapeutic area expert in both internal and external venues including the Medical Affairs sub-teams, and advisory boards / steering committees. Support various Medical Affairs cross-functional working groups. Represent Celgene at professional meetings, congresses, and local symposia. Support the planning and execution of Medical Affairs Sponsored Trials (MAST) and registries (as needed), within appropriate standards for compliance, quality, timeliness, and budget. Provide high quality scientific/clinical input and review of disease strategy plans, abstracts, posters, slides, manuscripts, educational materials, webcasts, IIT protocols, Commercial Brand plans, Scientific educational grant requests and patient advocacy grant requests. Track priority Medical Affairs tactics and performance to goals/budget. Partner with Scientific Communications on developing publication strategy, data gap analysis, and key messages. Assist with scientific searches, data summaries, preparation for site visits/corporate visits/payor presentations Interaction with key stakeholders, as a scientific and strategic expert.

Internal:

Medical Affairs partners in therapeutic area

Global Medical Affairs Leadership

Marketing

Market Access

Clinical

Statistics

Translational Research

Regulatory Affairs

Project Leadership

External:

Investigators, KOLs

Global steering committees

Scientific Advisory Boards

Advocacy groups

Cooperative groups

The ideal candidate will have the following mix of professional and personal characteristics:

Advanced degree in molecular biology, genomics, cancer biology or other relevant life sciences area.

Solid experience in clinical /translational research and/or medical affairs in hematology or oncology with 3 -5 years industry experience. Master’s degree holders with 5 years relevant industry experience may also apply.

Experience in the conduct of clinical trials in hematology/oncology preferred.

Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.

Experience with mining databases and other bioinformatics skills will be a strong plus.

Proficiency in scientific and clinical data review and interpretation.

Matrix leadership of cross-functional teams.

Strong organization skills.

Excellent oral and written communication skills, including presentations to large groups, facilitation of interactive discussions, and 1:1 discussion with thought leaders.

Demonstrated customer focus orientation & credibility with customers.

Knowledge/application of data sources, reports and tools for the creation of solid plans.

Possess experience creating and managing budgets

Regular travel will be required (approx 20%)

WORK ENVIRONMENT

Corporate office environment

Cross-functional interactions

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.

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Company info

Bristol-Myers Squibb Company
Website : http://www.bms.com