Senior Clinical Site Activation Lead

IQVIA; Wayne (PA); On-site; USD 94,000 - 157,000; Full time

Job summary

IQVIA seeks a Site Activation specialist to manage country-level SA activities, acting as the SPOC for investigative sites and project teams. You will ensure SOP/WIs adherence, document review, and timely activation in line with regulatory requirements.

Responsibilities include site feasibility, document preparation, data maintenance, and coordination of regulatory, ethics, IP releases, and project timelines. Strong communication and organizational skills are essential.

Qualifications

• Bachelor's Degree Life science or related field is required.
• 3 years clinical research experience, including 1 year in a leadership capacity.
• Equivalent combination of education, training and experience.

Responsibilities

• Serve as Single Point of Contact (SPOC) for sites and project teams under supervision.
• Perform feasibility, site ID, start up and site activation activities per SOPs.
• Prepare site documents and review for completeness and accuracy.
• Maintain internal systems and project tracking tools with site data.
• Monitor site performance metrics and advise on improvements.
• Coordinate regulatory documents, IP release, and timelines.

Skills

Clinical research

Leadership

Education

Bachelor's Degree Life science or related field

Job description

IQVIA seeks a Site Activation specialist to manage country-level SA activities, acting as the SPOC for investigative sites and project teams. You will ensure SOP/WIs adherence, document review, and timely activation in line with regulatory requirements.

Responsibilities include site feasibility, document preparation, data maintenance, and coordination of regulatory, ethics, IP releases, and project timelines. Strong communication and organizational skills are essential.