Senior Site Activation Lead

IQVIA; Durham (NC); On-site; USD 63,000 - 157,000; Full time

Job summary

IQVIA, a global leader in clinical research services, seeks a Site Activation Specialist to manage feasibility, site activation, and regulatory documentation at the country level. You will act as the SPOC for investigative sites, SAMs, and the Project Management team, ensuring SOP compliance and timely project deliverables.

The role requires a Life Sciences degree and 3 years of clinical research experience, including leadership experience.

Qualifications

• Bachelor’s degree in Life sciences or related field is required.
• 3 years clinical research experience, including 1 year in a leadership capacity, or an equivalent combo of education and experience.

Responsibilities

• Serve as Single Point of Contact (SPOC) for investigative sites, SAM, PM team and other departments.
• Perform feasibility, site ID, start-up and activation activities per regulations and SOPs.
• Prepare and review site documents for completeness and accuracy.
• Maintain internal systems and tracking tools with project information.
• Provide feedback on site performance metrics to management.
• Plan project timelines and monitoring measures; implement contingencies as needed.
• Track and follow up on document approvals and release processes (ICF, IP, CDA/SIF, etc.).
• Provide local expertise to SAMs and project team during timeline planning.
• Perform quality control of documents provided by sites.
• May have direct contact with sponsors for specific initiatives.

Education

Bachelor’s Degree Life science or related field

3 years clinical research experience, including 1 year experience in a leadership capacity

Job description

IQVIA, a global leader in clinical research services, seeks a Site Activation Specialist to manage feasibility, site activation, and regulatory documentation at the country level. You will act as the SPOC for investigative sites, SAMs, and the Project Management team, ensuring SOP compliance and timely project deliverables.

The role requires a Life Sciences degree and 3 years of clinical research experience, including leadership experience.