Bristol Myers Squibb
Director, Global Trial Lead(m/w/x)
Full-timeOn-siteSenior
Boudry
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BRBristol Myers Squibb
Senior Director, Clinical Development Leader(m/w/x)
Boudry
Full-timeOn-siteSenior
Nejo AI Summary
Leading clinical development strategies and managing physicians for novel oncology drugs. At least 10 years of MD experience required. Work-life balance programs, employee resource groups.
Requirements
- At least 10 years relevant experience MD required
- Deep understanding of clinical principles
- Demonstrated leadership in clinical trials design and execution
- Significant experience as senior clinical leader
- Synthesize data for clinical strategy
- Ensure viable registrational strategy
- Assess personnel needs and hiring strategy
- Ensure enterprise level strategy for assets and indications
- Demonstrated sustained excellent performance as Clinical Trial Physician
- Demonstrated sustained excellent performance as Clinical Scientist
- Verifiable track record of people management and development
- Leadership in a matrix team
- Excellent skills in clinical development strategy
- Clinical components of regulatory submission
- External focus on disease area treatment trends
- Ability to build relationships with external partners
- Ability to build relationships with thought leaders
- Partner with Early Development colleagues
- Assure seamless transition into late stage development
- Lead and develop CTP group
- Ensure scientific and technical excellence of programs
- Domestic and International travel may be required
- Encouraged to apply even if resume doesn't perfectly align
Tasks
- Lead and develop clinical development strategies
- Manage and motivate cross-functional teams
- Ensure clinical trials align with regulatory goals
- Directly manage clinical trial physicians
- Develop and retain top clinical talent
- Design and execute clinical studies
- Contribute to clinical content for regulatory documents
- Champion quality and compliance in clinical trials
- Represent Clinical Development in internal and external forums
- Partner with patient safety physicians for safety data review
- Co-lead cross-functional clinical development teams
- Provide clinical expertise in disease area strategies
- Collaborate with key opinion leaders
- Serve as primary clinical representative in regulatory interactions
- Evaluate strategic options against Target Product Profile
- Develop and manage asset-level risk plans
- Set and prioritize executional deliverables
- Support top-line data analysis and reporting
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Benefits
Other Benefits
- Competitive benefits
- Employee resource groups
- Reasonable workplace accommodations
Flexible Working
- Work-life balance programs
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bristol Myers Squibb and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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BRBristol Myers Squibb
Senior Director, Clinical Development Leader(m/w/x)
Boudry
Full-timeOn-siteSenior
Nejo AI Summary
Leading clinical development strategies and managing physicians for novel oncology drugs. At least 10 years of MD experience required. Work-life balance programs, employee resource groups.
Requirements
- At least 10 years relevant experience MD required
- Deep understanding of clinical principles
- Demonstrated leadership in clinical trials design and execution
- Significant experience as senior clinical leader
- Synthesize data for clinical strategy
- Ensure viable registrational strategy
- Assess personnel needs and hiring strategy
- Ensure enterprise level strategy for assets and indications
- Demonstrated sustained excellent performance as Clinical Trial Physician
- Demonstrated sustained excellent performance as Clinical Scientist
- Verifiable track record of people management and development
- Leadership in a matrix team
- Excellent skills in clinical development strategy
- Clinical components of regulatory submission
- External focus on disease area treatment trends
- Ability to build relationships with external partners
- Ability to build relationships with thought leaders
- Partner with Early Development colleagues
- Assure seamless transition into late stage development
- Lead and develop CTP group
- Ensure scientific and technical excellence of programs
- Domestic and International travel may be required
- Encouraged to apply even if resume doesn't perfectly align
Tasks
- Lead and develop clinical development strategies
- Manage and motivate cross-functional teams
- Ensure clinical trials align with regulatory goals
- Directly manage clinical trial physicians
- Develop and retain top clinical talent
- Design and execute clinical studies
- Contribute to clinical content for regulatory documents
- Champion quality and compliance in clinical trials
- Represent Clinical Development in internal and external forums
- Partner with patient safety physicians for safety data review
- Co-lead cross-functional clinical development teams
- Provide clinical expertise in disease area strategies
- Collaborate with key opinion leaders
- Serve as primary clinical representative in regulatory interactions
- Evaluate strategic options against Target Product Profile
- Develop and manage asset-level risk plans
- Set and prioritize executional deliverables
- Support top-line data analysis and reporting
Work Experience
- 10 years
Education
- Doctoral / PhD
Languages
- English – Business Fluent
Benefits
Other Benefits
- Competitive benefits
- Employee resource groups
- Reasonable workplace accommodations
Flexible Working
- Work-life balance programs
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bristol Myers Squibb and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Bristol Myers Squibb
Industry
Pharmaceuticals
Description
The company is dedicated to transforming patients’ lives through science and promotes global participation in clinical trials.
Not a perfect match?
- Bristol Myers Squibb
Director, Global Trial Lead(m/w/x)
Full-timeOn-siteSeniorBoudry - Takeda Manufacturing Austria AG
Associate Director, API Process Engineering(m/w/x)
Full-timeOn-siteManagementZürich, Neuenburg, Oranienburg - Bristol Myers Squibb
.Manager, Quality Operations(m/w/x)
Full-timeOn-siteExperiencedBoudry - Bristol Myers Squibb
Executive Director, Global Logistics Solutions Lead (EMEA)(m/w/x)
Full-timeOn-siteSeniorBoudry - INTEGRA LIFESCIENCES CORP
Quality Compliance Manager - ECMP Site Facilitator(m/w/x)
Full-timeOn-siteSeniorLe Locle, Rietheim-Weilheim