Associate Director, Trial Clinical Delivery Lead(m/w/x)

Requirements

• Bachelor’s Degree in Medical or Life Sciences
• 8-10 years clinical operations project management
• Expert knowledge of clinical development regulations
• Oncology, Neurology, or Immunology TA experience
• Clinical operations experience in CRO or pharma
• Strong interpersonal and communication skills
• Strategic thinking and influencing skills
• Ability to work independently
• Aptitude for interpreting analytical tools
• Risk assessment and decision-making ability
• Ability to oversee multiple tasks simultaneously
• Comfortable in fast-paced environments

Tasks

• Lead global clinical trial delivery and site performance
• Oversee site and vendor performance metrics
• Mitigate study risks and resolve operational issues
• Drive innovative methodologies and value-adding solutions
• Execute site and patient engagement strategies
• Coordinate between site leads and global functions
• Provide strategic oversight for Phase I-IIIb studies
• Promote data-driven planning and accountability
• Implement operational excellence strategies across studies
• Escalate trends and risks to senior management
• Onboard and train new clinical team members
• Facilitate regular communication with site stakeholders
• Lead process improvement and best practice initiatives
• Represent site management in clinical trial teams
• Assess data-driven proposals for country and site selection
• Integrate patient and physician insights into study design
• Design country start-up and recruitment strategies
• Implement decentralized clinical trial and digital solutions
• Manage service providers' timelines, budget, and quality
• Develop risk-based monitoring and site oversight plans
• Analyze performance data to ensure study quality
• Participate in investigator and study coordinator meetings

Education

Languages