Sr Site Activation Specialist
IQVIA · Durham, NC +2 more
Clinical OperationsFull-time$63k–$157kCompany career page
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Role summary
IQVIA seeks a Senior Site Activation Specialist to manage site activation activities for clinical research studies across multiple locations. The role involves coordinating between investigative sites, internal teams, and sponsors while ensuring regulatory compliance and project timelines are met.
What they're looking for
- Bachelor's degree in life science or related field
- 3+ years clinical research experience or equivalent education and training combination
- 1+ year experience in a leadership capacity
- Knowledge of site activation processes and regulatory requirements
- Proficiency with internal systems, databases, and tracking tools
- Strong communication and coordination skills across multiple stakeholders
What you'll be doing
- Serve as single point of contact for assigned studies between sites, managers, and project teams
- Execute feasibility, site identification, startup, and activation activities per regulations and SOPs
- Prepare and review site documents for completeness, accuracy, and quality control
- Maintain and update internal systems and databases with project-specific information
- Track progress and follow up on regulatory, ethics, consent, and investigator pack documents
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.