Bristol-Myers Squibb
Associate Medical Director, Eliquis Worldwide Medical Affairs
Bristol-Myers Squibb, Princeton, New Jersey, us, 08543
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.
Employer:
Bristol-Myers Squibb Company
Position:
Associate Medical Director, Eliquis Worldwide Medical Affairs (ref.# 4150)
Location:
3401 Princeton Pike, Lawrenceville, NJ 08648
Duties:Lead research and strategic planning to determine and develop a better understanding of unmet medical needs.Drive and engage in clinical investigation, research and development by leading the cross-functional Atrial Fibrillation (AF) Diagnosis Workstream in partnership with Alliance counterpart.Generate integrated evidence generation and communication plan for Diagnosis Workstream.Execute key projects with external stakeholders representing technology platforms as the internal scientific expert.Serve as functional area lead and scientific point for agency development of medical content for scientific venues including international congresses, advisory boards, scientific publications.Lead scientific development and conduct medical training for Worldwide (WW) field-based and HQ-based medical team members.Analyze emerging clinical data landscape and keep current with relevant therapeutic literature by attending conferences and meetings.Guide medical literacy across agency groups and provide understanding on cardiovascular (CV) disease states, clinical trials, treatment, and landscape competition by articulating effectively verbally and in writing complex scientific principles.Establish and maintain external scientific thought leader (physicians, scientists, and medical organizations) peer-to-peer relationships in the Diagnosis arena to identify additional areas to improve patient outcomes.Provide WW medical review of scientific content utilized in medical-to-medical and promotional materials and guide in-country teams for similar activities.Ensure that all medical affairs activities are compliant with policies and processes.Support Head of Eliquis WW Medical Affairs in development and oversight of the cross-matrix execution of the annual medical plan and associated medical deliverables.
Requirements:
Doctorate degree (or foreign equivalent) in medicine, biomedical engineering, pharmacy or life sciences plus 3 years of post-baccalaureate experience. Experience must include working in cross-functional teams in a highly matrixed environment and managing external agencies; generating, analyzing and interpreting clinical trial and published data; and scientific communication and presentation. The required skills do not need to be maintained over the full term of required experience to reflect demonstrable ability in the skill set described in the job duties.
Contact:
Althea WilsonEmail:
Resume.com@bms.com
Compensation:
The starting compensation for this job is a range from $161,500 to $218,500/year, 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.
Benefits:
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Career Site.
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 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.
Covid-19 Vaccination:
BMS 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.#J-18808-Ljbffr
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.
Employer:
Bristol-Myers Squibb Company
Position:
Associate Medical Director, Eliquis Worldwide Medical Affairs (ref.# 4150)
Location:
3401 Princeton Pike, Lawrenceville, NJ 08648
Duties:Lead research and strategic planning to determine and develop a better understanding of unmet medical needs.Drive and engage in clinical investigation, research and development by leading the cross-functional Atrial Fibrillation (AF) Diagnosis Workstream in partnership with Alliance counterpart.Generate integrated evidence generation and communication plan for Diagnosis Workstream.Execute key projects with external stakeholders representing technology platforms as the internal scientific expert.Serve as functional area lead and scientific point for agency development of medical content for scientific venues including international congresses, advisory boards, scientific publications.Lead scientific development and conduct medical training for Worldwide (WW) field-based and HQ-based medical team members.Analyze emerging clinical data landscape and keep current with relevant therapeutic literature by attending conferences and meetings.Guide medical literacy across agency groups and provide understanding on cardiovascular (CV) disease states, clinical trials, treatment, and landscape competition by articulating effectively verbally and in writing complex scientific principles.Establish and maintain external scientific thought leader (physicians, scientists, and medical organizations) peer-to-peer relationships in the Diagnosis arena to identify additional areas to improve patient outcomes.Provide WW medical review of scientific content utilized in medical-to-medical and promotional materials and guide in-country teams for similar activities.Ensure that all medical affairs activities are compliant with policies and processes.Support Head of Eliquis WW Medical Affairs in development and oversight of the cross-matrix execution of the annual medical plan and associated medical deliverables.
Requirements:
Doctorate degree (or foreign equivalent) in medicine, biomedical engineering, pharmacy or life sciences plus 3 years of post-baccalaureate experience. Experience must include working in cross-functional teams in a highly matrixed environment and managing external agencies; generating, analyzing and interpreting clinical trial and published data; and scientific communication and presentation. The required skills do not need to be maintained over the full term of required experience to reflect demonstrable ability in the skill set described in the job duties.
Contact:
Althea WilsonEmail:
Resume.com@bms.com
Compensation:
The starting compensation for this job is a range from $161,500 to $218,500/year, 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.
Benefits:
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit our BMS Career Site.
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 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.
Covid-19 Vaccination:
BMS 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.#J-18808-Ljbffr