Manager, Trial Delivery Management

• Execute study-level activities
• Create and update trial-specific documents, including Monitoring Guidelines, Informed Consent Forms, and investigational medicinal product documentation
• Set up and manage day-to-day study vendor activities, including statements of work and budget oversight
• Coordinate and oversee country- and regional-level trial management activities
• Align feasibility strategy with local teams and perform country-level risk reviews
• Support development of program-level compound training with Clinical and CTL&D Medical Writing
• Provide input into trial-level operational strategies
• Resolve trial-related issues and mitigate risks
• Participate in process improvement activities at trial, compound, and cross-DU levels
• Support Health Authority inspections and program-level risk and mitigation planning
• Mentor and support onboarding of new Trial Management team members
• Foster employee engagement, inclusion, and Credo Behaviors

• BS degree or equivalent; preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)
• Minimum of 8 years in Pharmaceutical, Healthcare, or related industries
• Experience in and knowledge of the pharmaceutical development process
• Clinical research operational knowledge and experience across multiple study phases (Phase I–IV)
• Ability to manage all aspects of clinical trial execution
• 2–3 years’ experience leading multiple aspects of a global clinical trial
• Excellent leadership skills and proven ability to foster team productivity and cohesiveness
• Experience leading without authority in multifunctional, matrixed, and global environments
• Excellent decision-making, analytical, and financial management skills
• Ability to operate and execute with limited supervision
• Experience mentoring/coaching others
• Strong project planning/management, communication, and presentation skills
• Ability to travel up to 15–20% of the time, as required by business needs
• Preferred industry experience:
  Pharmaceutical, Biopharmaceutical, Biotechnology

Demonstrates extensive experience in clinical trial execution and management, with a strong focus on operational strategies, risk mitigation, and team leadership. Proficient in creating trial-specific documentation and supporting health authority inspections within the pharmaceutical and healthcare sectors.

• Clinical Trial Execution
• Pharmaceutical Development Process
• Leadership in Global Clinical Trials
• Project Planning/Management
• Mentoring/Coaching

• Clinical Research Operational Knowledge
• Trial-Specific Documentation
• Budget Oversight
• Risk Mitigation Planning
• Feasibility Strategy Alignment
• Process Improvement Activities
• Decision-Making Skills
• Analytical Skills
• Financial Management Skills
• Study Phases Knowledge (Phase I–IV)

• Leadership Skills
• Team Productivity
• Communication Skills
• Presentation Skills
• Employee Engagement

• Pharmaceutical
• Healthcare
• Biopharmaceutical
• Biotechnology
• Life Sciences
• Clinical Trial Management
• Investigational Medicinal Product Documentation
• Informed Consent Forms
• Country-Level Risk Reviews
• Matrixed Environments