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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Director, Global Clinical Physician - Neuroscience

Biology & BiotechPosted on Nov 11
Full-timeUxbridge, UKNo salary listed

About the Job

Requirements

  • An MD or U.S.-equivalent degree is required.
  • At least 5 years of industry experience and/or clinical trials experience is required.
  • Ability to communicate information clearly and lead presentations in scientific and clinical settings.
  • Expertise in the scientific method for testing hypotheses, including statistical design, analysis, and interpretation.
  • Expertise in the drug development process.
  • Expertise in the components needed to execute effective clinical plans and protocols.
  • Strong leadership skills and the ability to lead and work effectively in a team environment.

Responsibilities

  • Contribute as a key member of a high-performing Study Delivery Team and potentially as a member of the Clinical Development Team.
  • Lead medical data review of trial data, including eligibility review.
  • Manage site interactions with the Clinical Scientist on medical questions and education, including safety management guidelines.
  • Assess key safety-related serious adverse events with Worldwide Patient Safety and oversee safety narratives.
  • Collaborate with Clinical Scientists and provide medical strategic oversight and input into protocols, including inclusion/exclusion criteria and other safety-related clinical considerations.
  • Fulfill Good Clinical Practice and compliance obligations for clinical conduct and maintain required training.
  • Collaborate with the Clinical Development Lead to design and develop clinical plans and protocols based on knowledge of the asset or drug, disease area, and relevant science, supporting regulatory and disease strategy targets.
  • Provide medical oversight and accountability for a group of studies.
  • Lead benefit-risk analysis for clinical development protocols in a matrix team environment with Clinical Scientists.
  • Partner with Clinical Scientists to support study execution, including site activation, enrollment status, and adjudication of protocol violations and significant or non-significant deviations.
  • Identify and build relationships with principal investigators, and cultivate thought leaders to obtain input on emerging science in drug and biomarker research, disease knowledge, and clinical development study and program design.
  • Maintain a strong medical and scientific reputation in the disease area through in-depth knowledge of its etiology, natural history, diagnosis, and treatment, including conference attendance and ongoing literature review.
  • Monitor development and regulatory issues related to competitive or relevant compounds and assess the portfolio's competitive landscape.
  • Provide ongoing medical education with Clinical Scientists, including protocol-specific training for study teams, investigators, and others.
  • Serve as a medical point of expertise in key Health Authority interactions and advisory board meetings as a Senior Clinical Trial Physician.
  • Author or draft clinical content for clinical study reports, regulatory reports, briefing books, and submission documents to support study closure, clinical narratives, reporting, and filing.

Desired Qualifications

  • Subspecialty training in an applicable therapeutic area.

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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