Associate Site Activation Manager
IQVIA · Durham, NC +3 more
Clinical OperationsFull-time$60k–$157kCompany career page
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Role summary
IQVIA seeks an Associate Site Activation Manager to direct and manage site activation strategies, regulatory processes, and operational delivery for clinical trials across multiple regions. The role combines project oversight, stakeholder collaboration, and regulatory expertise to accelerate site identification and patient enrollment.
What they're looking for
- Bachelor's degree in life science or related field
- At least 3 years of experience in scientific or clinical environment
- Demonstrable international role experience or equivalent combination
- In-depth knowledge of clinical systems, procedures, and corporate standards
- Strong medical terminology and regulatory knowledge
- Proficiency in Microsoft Office and email applications
- Ability to manage multiple projects independently and prioritize effectively
What you'll be doing
- Provide strategic planning and project oversight to accelerate site activation and patient enrollment
- Oversee start-up execution and lifecycle maintenance for assigned studies in compliance with regulatory requirements
- Develop, implement, and maintain site activation management plans with key stakeholder collaboration
- Execute operational strategy for clinical study approvals and review contracts and essential documents
- Assess regulatory landscape, determine submission strategy, and provide ongoing reporting to organizational leadership
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.