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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Director, Translational Medicine - Neurology

Biology & BiotechConfirmed live in the last 24 hours
Full-time

About the Job

Requirements

  • PhD or MD/PhD in neuroscience and at least 10 years of translational medicine experience.
  • At least 7 years of late-stage clinical biomarker experience in biotech or pharmaceutical organizations.
  • Recognized expertise in translational biomarkers in neurology.
  • Experience in late-stage drug development and activities related to clinical trial initiation, maintenance, and completion.
  • Strong verbal and written communication skills.
  • Experience interacting with contract research organizations and academic thought leaders to manage projects and timelines.
  • Scientific and leadership expertise, including working in teams, mentoring people, and managing projects.
  • Ability to prioritize risks and implement contingency plans.
  • Ability to provide expert guidance to multidisciplinary teams and senior management, deliver results, drive continuous improvement, and build effective cross-functional networks.

Responsibilities

  • Design and implement program-specific late-development biomarker and translational plans; aid in creating clinical protocols, statistical analysis plans, statements of work, and lab manuals; and interface with contract research organizations to execute services alongside Biospecimen Operations and Procurement.
  • Determine appropriate assays and vendors for clinical biomarkers, and manage outsourcing of biomarker assay development and validation in partnership with Translational Sciences colleagues when applicable.
  • Manage clinical biomarker data delivery, analysis, and associated timelines by working with relevant internal functions and contract research organizations.
  • Prepare and deliver internal and external translational and biomarker presentations.
  • Maintain timelines for biomarker-data-related publications through interaction with Medical Communications and the Publications team as needed.
  • Keep current with relevant scientific and technical literature, apply external knowledge to internal research programs as appropriate, and critically evaluate literature regarding the asset and disease biology as a subject-matter expert within the team.
  • Work with translational medicine laboratory scientists and academic thought leaders to address nonclinical translational questions.
  • Participate in post-hoc biomarker analysis and publication efforts.
  • Support regulatory submissions and regulatory interactions as needed.
  • Serve as translational lead for neurological and neuropsychiatric indications, setting strategy for translational activities, including clinical biomarker activities supporting drug development programs.
  • Represent translational medicine on global program teams and biomarkers on study teams; develop biomarker plans for individual trials and ensure appropriate collection, timely analysis, and reporting of final biomarker data.
  • Answer key translational medicine questions related to assigned assets and diseases in collaboration with the translational medicine laboratory team and academic thought leaders.
  • Communicate regularly and prepare and deliver presentations within the department, to governance and senior leadership bodies, and externally as requested.
  • Recognize cross-functional issues and communicate them within the larger organization.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

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