Bristol Myers Squibb
Manager - Site procurement(m/w/x)
Vollzeit
Senior
Keine Angabe
Boudry
BR
Bristol Myers Squibb1 Monat
Director, Global Trial Lead(m/w/x)
Vollzeit
Senior
AI/ML Job
Keine Angabe
Boudry
Nejo KI-Zusammenfassung
As the Director, Global Trial Lead, you will oversee the strategic execution of global clinical trials, ensuring high-quality data and compliance while fostering innovation and collaboration across teams. This role involves managing complex projects, mentoring future leaders, and driving operational excellence to support the growth strategy.
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Anforderungen
- •Advanced degree (MS, PharmD, PhD, MD, or equivalent) preferred
- •BA/BS required
- •Minimum 10 years of experience in clinical operations and global project management
- •Multi-national experience
- •Experience in leading global clinical trials and programs at the Director level
- •Experience leading global and multi-functional study teams
- •Experience in managing CROs and external partners at a strategic level preferred
- •Proficiency in AI tools and familiarity with technological advancements preferred
- •Travel requirement: up to 25%
- •Ability to physically travel to visit customers, patients or business partners
Master-Abschluss
ODER
Bachelor-Abschluss
Berufserfahrung
10 Jahre
Deine Aufgaben
- •Provide leadership for complex clinical trials
- •Ensure delivery of high-quality data and regulatory compliance
- •Collaborate with internal teams and vendors for trial delivery
- •Oversee operational activities and study feasibility
- •Make decisions on complex issues and manage risks
- •Manage study budgets, contracts, and scope of work
- •Participate in vendor selection and evaluation
- •Oversee vendor relationships and ensure alignment
- •Set and monitor performance metrics for trials
- •Utilize quality indicators to optimize trial execution
- •Maintain accurate data records in study management systems
- •Establish project management tools for studies
- •Develop trial-specific standards for operational consistency
- •Lead organizational change initiatives and best practices
- •Foster cross-functional collaboration for knowledge sharing
- •Champion innovative solutions for trial acceleration
- •Define strategic direction for clinical trial execution
- •Provide guidance on study protocols and execution strategies
- •Monitor trends in clinical operations and advise teams
- •Mentor GDO Study Team members and future leaders
- •Promote a high-performing team culture and collaboration
- •Model ethical behavior and commitment to learning
- •Drive upfront planning of study timelines and budgets
- •Lead quarterly budget reviews and flag variances
- •Approve and reconcile vendor invoices and amendments
- •Identify and resolve budget and timeline issues
- •Manage study logistics and escalate resourcing needs
- •Oversee execution of multiple clinical trials
- •Provide lifecycle leadership from start-up to close-out
- •Analyze operational metrics for study optimization
- •Identify challenges and propose actionable solutions
- •Build partnerships with internal and external stakeholders
- •Lead global clinical trials with strategic oversight
- •Ensure compliance with regulatory standards and patient safety
- •Manage end-to-end trial operations and resource planning
- •Mitigate risks to ensure trial continuity and delivery
- •Demonstrate diplomacy in interfacing with stakeholders
- •Utilize clinical systems to track milestones and data quality
- •Lead large cross-functional teams toward shared goals
- •Support mentoring of new GTL team members
- •Exhibit critical thinking and problem-solving skills
- •Make informed decisions in high-pressure environments
- •Communicate effectively with cross-functional teams
- •Build trust-based relationships with diverse stakeholders
Tools & Technologien
AI tools
Sprachen
Englisch – verhandlungssicher
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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