Lead Hematology Medical Data Generation

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.

Qualifications:

Overall responsibility for Hematology conduct of studies/trials that are investigator-sponsored or medically-led

Responsible for overseeing the writing and monitoring of BMS-sponsored, medically-led research studies and ensures their timely accrual and completion

Chair Review Committees (or provide oversight where appropriate) for investigator-sponsored research studies and BMS-sponsored, medically-led research studies

Approves final protocols, amendments and budgets for studies under remit

Interface with WW Medical Disease-based teams in the Integrated Development plan

Serve as the subject matter expert on the current book of work for studies under remit and give updates to key stakeholders across the organization

Oversee the development and renewal of areas of interest for investigator-sponsored research studies through cross-functional interface with key global and regional stakeholders

Clinical decision-making responsibility for all studies within remit, including safety queries, departures from standard inclusion/exclusion criterion and questions/concerns from investigators and internal team members arising from patients on study

Supervising and mentoring Clinical Trial Leads within reporting line

Meet with investigators and cross-functional internal team involved in studies under remit to discuss barriers, budget concerns, and/or data readouts

Meet with investigators and cross-functional internal team involved in studies under remit to discuss barriers, budget concerns, and/or data readouts.

Requirements:

MD preferred, with 5 years of clinical trial experience; non-MD applicants with a strong track record of clinical trial experience in the pharmaceutical industry will be considered

Demonstrated track record of leadership in a complex, matrix environment; experience delivering successful results in a variety of business situations

Excellent communication skills and experience with difficult discussions

Demonstrate strong decision-making skills

Successful track record of leading through influence and working across complex, global organizational matrices

HQ based position with travel requirement of 25% dependent on the state of future congress attendance.

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