Site Activation Lead, Clinical Trials

IQVIA LLC

Durham (NC)

On-site

USD 63,000 - 157,000

Full time

7 days ago

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Job summary

IQVIA in Durham, NC is seeking a Site Activation professional to manage country-level SA activities, coordinating with the SAM and project teams to ensure SOPs, WIs, and timelines are followed. You will drive feasibility, site ID, start-up and activation efforts and distribute documents to sites and colleagues for timely progress.

You will review and prepare site documents, maintain data systems, monitor metrics, and provide local expertise during planning.

Qualifications

Bachelor's Degree in Life Science or related field is required.
3 years of clinical research experience, including 1 year in a leadership capacity is required.

Responsibilities

Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, SAM, and project teams.
Perform feasibility, site ID, start up and activation activities per regulations and SOPs; distribute documents to sites and team.
Prepare site documents and review for completeness and accuracy.
Maintain internal systems, databases and tracking tools with project data.
Review site performance metrics and provide feedback to management.
Plan and monitor project timelines; implement contingency plans as needed.
Inform team of completion of feasibility, site ID, regulatory and contractual documents.
Provide local expertise to SAMs and project team during planning.
Perform quality control of documents from sites.
May have direct contact with sponsors on specific initiatives.