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
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 3 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
Benefits
Sonstige Vorteile
- Competitive benefits
- Employee resource groups
- Reasonable workplace accommodations
Flexibles Arbeiten
- Work-life balance programs
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Bristol Myers Squibb erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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Nejo KI-Zusammenfassung
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.
Anforderungen
- 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
Aufgaben
- 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
Berufserfahrung
- 3 Jahre
Ausbildung
- Doktor / Ph.D.
Sprachen
- Englisch – verhandlungssicher
Benefits
Sonstige Vorteile
- Competitive benefits
- Employee resource groups
- Reasonable workplace accommodations
Flexibles Arbeiten
- Work-life balance programs
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens Bristol Myers Squibb erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Bristol Myers Squibb
Branche
Pharmaceuticals
Beschreibung
The company is dedicated to transforming patients’ lives through science and promotes global participation in clinical trials.
Noch nicht perfekt?
- Bristol Myers Squibb
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