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Bristol Myers Squibb Clinical Trial Lead, Myeloid Diseases, Medical Data Generation in Lawrence Township, New Jersey

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Position Summary

Clinical Trial Lead, Myeloid Diseases will be responsible for driving the development, tracking, and maintenance of the Integrated Evidence Plans for the Myeloid assets. Additionally, he/she will provide the day-to-day oversight and conduct of the Investigator Sponsored Research (ISR) Book of Work for Myeloid assets.

Key Responsibilities

  • Lead the development, tracking, and maintenance of the Integrated Evidence Plans (IEP) and facilitate the cross-functional alignment for assets in Myeloid, in the form of slide decks and/or tech enablement platform

  • Develop IEP(s) that reflects asset strategy, market priorities, and Medical Data Generation support (investigator vs company sponsored research) in partnership with the Myeloid Global Medical Disease Team and cross-functional teams including (but not limited to) Global Drug Development (GDD), Translational Development, HEOR, and others

  • Develop Areas of Interest (AOI) based on key open data questions (ODQ) identified in the IEP with market input in collaboration with the Myeloid Global Medical Disease Team

  • Assess and identify any disease area gaps not addressed by the IEP(s)

  • Responsible for ongoing Myeloid ISR work, including non-clinical research studies and serve as the subject matter expert and interface with all key stakeholders across the matrix, including (but not limited) to Worldwide and Local Medical, Global Development Operations (GDO), GDD, Field Medical, Commercial, and HEOR

  • Conduct regular book of work reviews in partnership with GDO with key medical and development stakeholders, under their remit

  • Interface with Market contacts (Field Medical and/or Medical) on the conduct of ongoing ISRs, as well as new and concepts/protocols in development

  • Partner with Business Insights and Analytics for acquiring metrics on ongoing studies and the development of visualization tools to analyze the performance of the ongoing book of work.

  • Identify studies at risk for failing to meet timelines and negotiated mitigation plans with key internal stakeholders and investigators

  • Accountable for ISR data reporting and major congresses to inform medical capabilities and other internal stakeholders

  • Assist in the reviews of concepts through RFP process, as appropriate, including providing context for ongoing book of work, area of interest development, and upcoming data read-outs

  • Chair concept reviews, as delegated

Qualifications & Experience

  • PharmD, PhD or MD

  • 2+ years of experience with Investigator Initiated Clinical Trial oversight

Key Competency Requirements

  • 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

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

Travel Required

  • Domestic and International travel may be required

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or 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.

Company: Bristol Myers Squibb

Req Number: R1541390

Updated: 2021-06-15 09:45:06.261 UTC

Location: Lawrence Township,New Jersey

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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