Bristol Myers Squibb
Senior Director, Clinical Development Leader(m/w/x)
Vollzeitnur vor OrtSenior
Boudry
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BRBristol Myers Squibb
Director, Global Clinical Physician(m/w/x)
Boudry
Full-timeOn-siteExperienced
Nejo AI Summary
Medical accountability for Phase 1-3 drug development studies, reviewing medical data and trial eligibility. MD or equivalent with subspecialty training and scientific method expertise required. 4-day work week, company car for private use.
Requirements
- MD or equivalent
- Clear scientific and clinical communication
- Subspecialty training in applicable therapeutic area
- Expertise in scientific method and statistical analysis
- Knowledge of drug development process
- Knowledge of clinical plan and protocol execution
- Strong leadership and teamwork skills
Tasks
- Serve as primary medical accountability for clinical trials
- Manage Phase 1-3 studies with decision-making capabilities
- Provide medical and scientific expertise to cross-functional teams
- Contribute to high-performing Study Delivery Teams
- Review medical data and trial eligibility
- Interact with clinical trial sites for medical questions and education
- Assess and manage safety-related serious adverse events
- Collaborate on protocol development and medical strategic oversight
- Fulfill GCP and compliance obligations
- Design and develop clinical plans and protocols
- Provide medical oversight for a group of studies
- Lead benefit/risk analysis for clinical development protocols
- Support study execution, including site activation and enrollment
- Build relationships with principal investigators and thought leaders
- Maintain medical and scientific reputation in the disease area
- Stay updated on disease etiology, diagnosis, and treatment
- Attend scientific conferences and review literature
- Monitor competitive landscape and regulatory issues
- Provide medical education and protocol-specific training
- Participate in Health Authority interactions and advisory board meetings
- Author clinical content for reports and regulatory submissions
Work Experience
- 3 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
Director, Global Clinical Physician(m/w/x)
Boudry
Full-timeOn-siteExperienced
Nejo AI Summary
Medical accountability for Phase 1-3 drug development studies, reviewing medical data and trial eligibility. MD or equivalent with subspecialty training and scientific method expertise required. 4-day work week, company car for private use.
Requirements
- MD or equivalent
- Clear scientific and clinical communication
- Subspecialty training in applicable therapeutic area
- Expertise in scientific method and statistical analysis
- Knowledge of drug development process
- Knowledge of clinical plan and protocol execution
- Strong leadership and teamwork skills
Tasks
- Serve as primary medical accountability for clinical trials
- Manage Phase 1-3 studies with decision-making capabilities
- Provide medical and scientific expertise to cross-functional teams
- Contribute to high-performing Study Delivery Teams
- Review medical data and trial eligibility
- Interact with clinical trial sites for medical questions and education
- Assess and manage safety-related serious adverse events
- Collaborate on protocol development and medical strategic oversight
- Fulfill GCP and compliance obligations
- Design and develop clinical plans and protocols
- Provide medical oversight for a group of studies
- Lead benefit/risk analysis for clinical development protocols
- Support study execution, including site activation and enrollment
- Build relationships with principal investigators and thought leaders
- Maintain medical and scientific reputation in the disease area
- Stay updated on disease etiology, diagnosis, and treatment
- Attend scientific conferences and review literature
- Monitor competitive landscape and regulatory issues
- Provide medical education and protocol-specific training
- Participate in Health Authority interactions and advisory board meetings
- Author clinical content for reports and regulatory submissions
Work Experience
- 3 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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.
Noch nicht perfekt?
- Bristol Myers Squibb
Senior Director, Clinical Development Leader(m/w/x)
Vollzeitnur vor OrtSeniorBoudry - Bristol Myers Squibb
Director, Global Trial Lead(m/w/x)
Vollzeitnur vor OrtSeniorBoudry - Bristol Myers Squibb
Regional Medical Market TA Lead - Europe Cardiovascular(m/w/x)
Vollzeitnur vor OrtSeniorBoudry - Bristol Myers Squibb
.Manager, Quality Operations(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBoudry - Bristol Myers Squibb
Manager, Customer Partnership & Supply Orchestration (CPSO) Launch Excellence(m/w/x)
Vollzeitnur vor OrtSeniorBoudry