Field Medical Director, Cell Therapy Central Region
Working with UsChallenging.
Meaningful.
Life-changing.
Those aren t 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.
You ll 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:
careers.
bms.
com/working-with-us.
The Field Medical Director, US Medical Affairs will report to the VP of USM Hematology.
He/she will be field based but expected to attend headquarter based activities in Summit, New Jersey (up to 25%).
This individual will represent US Medical as therapeutic area expert in Cell Therapy and provide clinical/scientific leadership and support for approved CAR T products as well as Cell Therapy compounds in various stages of clinical development.
He/she will be accountable for the oversight of the nonconformed CAR T expanded access protocols including taking the role as the clinical trial physician as indicated.
He/she will be accountable for the clinical research scientist(s) overseeing the EAP studies.
He/she will provide clinical expertise and support for the CART CIBMTR registries.
He/she will assist the CAR T Field Medical team with site on boarding activities including training in collaboration with the CAR T Field Medical directors, scientific directors and disease leads.
This individual s responsibilities will include strategic and tactical planning of medical Cell Therapy program site support and provide oversight for the FMDs who are the point of contact for internal site launch experience.
He/she will need to have the capability to travel and provide on-site support for designated CAR T sites as needed in collaboration with the Field Medical directors and medical field team.
He/she will represent US Medical as needed, serving as a therapeutic area expert in Cell Therapy products.
Responsibilities will include, but are not limited to, the following:
Medical director point of contact for field medical team (MSL) and CAR T sites within designated region.
Ensure positive first CAR T clinical experience for each product at individual sites.
Ensure sites continue to meet certification criteria after initial certification.
Point of contact for escalated calls from HCPs treating patients with BMS CAR T products that come thru the 24hr/7day call center or medical unsolicited requests.
Assist the field medical team (MSL) and cross-functional partners during CAR T program site qualification and certification process.
In collaboration with the MSL national director, ensure all CAR T sites have medical support.
Assist and lead post-launch CART site support and strategy in collaboration with the field medical team (MSL).
Point of contact for clinical issues related to nonconforming products including participation in internal material review board and primary medical person responsible to communicate information to treating physicians related to nonconforming products.
Collaborate in the development of training materials for sites and medical field team and provide training for both external and internal stakeholders including REMS.
Lead and support various Medical cross-functional working groups with priority to activities related to CAR T site qualification, verification and post-launch CAR T site support.
Responsible for refining strategies and identify best practices for optimal medical support for Cell Therapy programs.
Understand and develop site points of pain problem lists with clinical relevance.
Develop tools to assist sites in ease and quality of care to patients.
Work with EMR support/clinical pathways.
Collaborate with Medical launch leads to define, guide and execute CAR T strategies and tactics with appropriate use of resources.
Support CAR T medical affairs studies (e.
g.
registries, protocols).
Provide therapy area medical and scientific expertise to clinical study teams and key stakeholders.
Represent the US Medical Affairs as a therapeutic expert at ad boards and steering committee.
Represent BMS at professional meetings, congresses, and local symposia.
In collaboration with field medical team (MSL), lead and execute on external KOL engagement plan.
Cultivate and nurture strong collaborations, relationships and support with Investigators, Academic partners and KOL s.
Provide high quality clinical input and review of the following but not limited to:
CAR T strategy plans, abstracts, posters, slides, manuscripts, educational materials, steering committee and advisory board meeting objectives, Medical information letters, and Commercial Brand plans.
The ideal candidate will have the following mix of professional and personal characteristics:
MD, preferable with clinical, research and/or industry experience in cellular therapy and Hematology/Oncology.
A minimum of 5-7 years academic/industry experience strongly preferred.
Expertise in cellular therapy/hematopoietic stem cell transplantation and/or hematological malignancies is a strong plus.
Demonstrate clinical management knowledge and skills.
Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.
Proficiency in critical data review and interpretation.
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 and credibility with customers.
Knowledge/application of data sources, reports and tools for the creation of solid plans.
Regular travel will be required ( approx.
75%).
Demonstrated ability to work as part of a team and problem solving skills.
The starting compensation for this job is a range from $173,000 $217,000, plus incentive cash and stock opportunities (based on eligibility).
The starting pay takes into account characteristics of the job, such as required skills and where the job is performed.
Final, individual compensation is decided based on demonstrated experience.
For more on benefits, please visit our BMS Careers site.
Eligibility for specific benefits listed in our careers site may vary based on the job and location.
#LI-RemoteIf you come across a role that intrigues you but doesn t 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 CareersWith 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 adastaffingsupport@bms.
com.
Visit careers.
bms.
com/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.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
Meaningful.
Life-changing.
Those aren t 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.
You ll 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:
careers.
bms.
com/working-with-us.
The Field Medical Director, US Medical Affairs will report to the VP of USM Hematology.
He/she will be field based but expected to attend headquarter based activities in Summit, New Jersey (up to 25%).
This individual will represent US Medical as therapeutic area expert in Cell Therapy and provide clinical/scientific leadership and support for approved CAR T products as well as Cell Therapy compounds in various stages of clinical development.
He/she will be accountable for the oversight of the nonconformed CAR T expanded access protocols including taking the role as the clinical trial physician as indicated.
He/she will be accountable for the clinical research scientist(s) overseeing the EAP studies.
He/she will provide clinical expertise and support for the CART CIBMTR registries.
He/she will assist the CAR T Field Medical team with site on boarding activities including training in collaboration with the CAR T Field Medical directors, scientific directors and disease leads.
This individual s responsibilities will include strategic and tactical planning of medical Cell Therapy program site support and provide oversight for the FMDs who are the point of contact for internal site launch experience.
He/she will need to have the capability to travel and provide on-site support for designated CAR T sites as needed in collaboration with the Field Medical directors and medical field team.
He/she will represent US Medical as needed, serving as a therapeutic area expert in Cell Therapy products.
Responsibilities will include, but are not limited to, the following:
Medical director point of contact for field medical team (MSL) and CAR T sites within designated region.
Ensure positive first CAR T clinical experience for each product at individual sites.
Ensure sites continue to meet certification criteria after initial certification.
Point of contact for escalated calls from HCPs treating patients with BMS CAR T products that come thru the 24hr/7day call center or medical unsolicited requests.
Assist the field medical team (MSL) and cross-functional partners during CAR T program site qualification and certification process.
In collaboration with the MSL national director, ensure all CAR T sites have medical support.
Assist and lead post-launch CART site support and strategy in collaboration with the field medical team (MSL).
Point of contact for clinical issues related to nonconforming products including participation in internal material review board and primary medical person responsible to communicate information to treating physicians related to nonconforming products.
Collaborate in the development of training materials for sites and medical field team and provide training for both external and internal stakeholders including REMS.
Lead and support various Medical cross-functional working groups with priority to activities related to CAR T site qualification, verification and post-launch CAR T site support.
Responsible for refining strategies and identify best practices for optimal medical support for Cell Therapy programs.
Understand and develop site points of pain problem lists with clinical relevance.
Develop tools to assist sites in ease and quality of care to patients.
Work with EMR support/clinical pathways.
Collaborate with Medical launch leads to define, guide and execute CAR T strategies and tactics with appropriate use of resources.
Support CAR T medical affairs studies (e.
g.
registries, protocols).
Provide therapy area medical and scientific expertise to clinical study teams and key stakeholders.
Represent the US Medical Affairs as a therapeutic expert at ad boards and steering committee.
Represent BMS at professional meetings, congresses, and local symposia.
In collaboration with field medical team (MSL), lead and execute on external KOL engagement plan.
Cultivate and nurture strong collaborations, relationships and support with Investigators, Academic partners and KOL s.
Provide high quality clinical input and review of the following but not limited to:
CAR T strategy plans, abstracts, posters, slides, manuscripts, educational materials, steering committee and advisory board meeting objectives, Medical information letters, and Commercial Brand plans.
The ideal candidate will have the following mix of professional and personal characteristics:
MD, preferable with clinical, research and/or industry experience in cellular therapy and Hematology/Oncology.
A minimum of 5-7 years academic/industry experience strongly preferred.
Expertise in cellular therapy/hematopoietic stem cell transplantation and/or hematological malignancies is a strong plus.
Demonstrate clinical management knowledge and skills.
Excellent analytical skills and solid experience in translating medical/clinical information into medical affairs strategies.
Proficiency in critical data review and interpretation.
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 and credibility with customers.
Knowledge/application of data sources, reports and tools for the creation of solid plans.
Regular travel will be required ( approx.
75%).
Demonstrated ability to work as part of a team and problem solving skills.
The starting compensation for this job is a range from $173,000 $217,000, plus incentive cash and stock opportunities (based on eligibility).
The starting pay takes into account characteristics of the job, such as required skills and where the job is performed.
Final, individual compensation is decided based on demonstrated experience.
For more on benefits, please visit our BMS Careers site.
Eligibility for specific benefits listed in our careers site may vary based on the job and location.
#LI-RemoteIf you come across a role that intrigues you but doesn t 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 CareersWith 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 ProtocolPhysical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
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 adastaffingsupport@bms.
com.
Visit careers.
bms.
com/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.
.
Estimated Salary: $20 to $28 per hour based on qualifications.
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