Senior Global Clinical Scientist — Trials Lead

Bristol Myers Squibb EU Policy

Madison (NJ)

On-site

USD 151,000 - 183,000

Full time

35 hours ago
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Job summary

Bristol Myers Squibb is seeking a Senior Manager, Global Clinical Scientist to design and deliver clinical studies in neuroscience. You will collaborate with cross-functional teams, lead trial activities, and drive data review plans in partnership with Data Management and Programming.

The role requires expertise in GCP/ICH, clinical operations, and medical writing, with strong communication skills to interact with external partners and governance committees.

Qualifications

  • Degree in Life Sciences or equivalent; MD/PhD/PharmD/MS/RN preferred.
  • Knowledge of GCP/ICH, drug development, study design and statistics.
  • Experience in clinical operations and medical writing is expected.
  • Strong planning and project management skills are required.

Responsibilities

  • Design and execute assigned clinical trial activities and collaborate with the clinical team.
  • May serve as Clinical Trial Lead for one or more trials.
  • Lead or support trial activities with appropriate supervision.
  • Co-lead study team meetings and coordinate with governance committees.
  • Develop Protocol and ICF documents and present to governance meetings.
  • Submit clinical contributions to CSRs and regulatory documents.

Skills

GCP/ICH knowledge
Clinical study design
Medical writing
Data monitoring & review
Project management
Regulatory documentation
Cross-functional collaboration
MS Office tools

Education

Life sciences degree (MD/PhD/PharmD/MS/RN or equivalent)

Tools

Pt Profiles
Report generating tools

Job description

Bristol Myers Squibb is seeking a Senior Manager, Global Clinical Scientist to design and deliver clinical studies in neuroscience. You will collaborate with cross-functional teams, lead trial activities, and drive data review plans in partnership with Data Management and Programming.

The role requires expertise in GCP/ICH, clinical operations, and medical writing, with strong communication skills to interact with external partners and governance committees.

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