Description
Make an impact on patient health!
IQVIA's Global Site Activation Team drives best-in-class site and customer experiences with industry-leading outcomes. As a Site Activation Coordinator, you will execute site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the country level.
Job Responsibilities
- Serve as a Single Point of Contact (SPOC) to perform site activation and maintenance activities in assigned studies for investigative sites, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.
- Prepare site documents, review for completeness and accuracy.
- Inform team members of completion of regulatory, contractual, and other documents for individual sites.
- Distribute completed documents to sites and internal project team members.
- Update and maintain internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
- Review, track, and follow up on the progress, approval, and execution of required documents.
Qualifications
- Bachelor's Degree in Life Sciences or a related field.
- Desirable: 1-3 years of clinical research or other relevant experience; or equivalent combination of education, training, and experience.
Benefits
- Exposure across 21 Therapeutic Areas
- Be part of a global team operating across 141 locations
- Exposure across a variety of studies and projects
- Access to new, innovative technologies
- Work within a collaborative and vibrant environment
- Own your career!
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. They create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
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