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

Description

You will drive the success of global clinical trials by providing strategic leadership and innovative oversight. From designing patient-centric recruitment strategies to managing vendor performance, you'll ensure high-quality study delivery.

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

Benefits