Scientific Director, US Medical Affairs, Lymphoma

1 week ago


Madison, New Jersey, United States Bristol-Myers Squibb Full time

**Working with Us**

Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Youll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

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 with the resources to pursue their goals, both at work and in their personal lives. Read more: .

Scientific Director, US Medical CT Lisocel will report to the, US Disease Lead. He/she will be headquarters based with field responsibilities to support CAR T field medical team , and will provide scientific/medical leadership and support for compounds in various stages of clinical development, as well as approved products in that therapeutic area for cell therapy. This individual will support the design and implementation of a strategic disease area medical plan, under the direction of the US Disease Lead, and in coordination with the US PAN CART Team. They will serve as disease expert. They will also take a leadership role for the execution/support of BMS sponsored medical affairs trials (as needed) and registries and will also assist in the evaluation and support of investigator-initiated trials.

He/she will represent US Medical Affairs as needed on behalf of the US Disease Lead, serving as a therapeutic area expert in scientific, strategic and tactical discussions and presentations with internal colleagues as well as with external experts and investigators. Responsibilities will include, but are not limited to, the following: 1. Collaborate with Medical Affairs colleagues to guide and execute therapeutic area strategy.

**Position Responsibilities**

+ Collaborate with Medical Affairs colleagues to guide and execute therapeutic area strategy and tactics with appropriate use of resources

+ Assist US Disease Lead as necessary for various activities Represent US Medical Affairs on behalf of the Disease

+ Lead as a therapeutic area expert in both internal and external venues including Medical Affairs sub-teams, and advisory boards / steering committees Lead/support various Medical Affairs cross-functional working groups including support to the CAR T MSL with site onboarding, activation and maintenance

+ Represent BMS at professional meetings, congresses, and local symposia. Drive 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

+ Lead/Track priority Medical Affairs tactics and performance to goals/budget & develop functional lymphoma budget/plan Partner with Scientific Communications on developing publication strategy, 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:

**Required Qualifications & Experience**

+ Advanced degree in medicine, 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 7-10 years of clinical, academic/industry experience. Masters degree holders with 10+ 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 discussions 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 25%)

**#LI-Hybrid**

_If you come across a role that intrigues you but doesnt perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career._

**Uniquely Interesting Work, Life-changing Careers**

With a single vision as inspiring as Transforming patients lives through science , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

**On-site Protocol**

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit ) eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

**Company:** Bristol-Myers Squibb

**Req Number:** R

**Updated:** :00:57.850 UTC

**Location:** Madison-NJ

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, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.



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