Site Activation & Contract Negotiation Specialist

IQVIA; Lexington (KY); On-site; USD 49,000 - 123,000; Full time

Job summary

IQVIA is seeking a candidate to support feasibility, site activation, regulatory start-up, and ongoing maintenance activities at regional or country levels. The role involves preparing site documentation, reviewing contracts, and tracking performance metrics while ensuring all activities comply with regulations and SOPs.

Under moderate supervision, you will coordinate with the Project Management team and other departments, review regulatory and ethics approvals, and help establish timelines for

Qualifications

• Comprehensive knowledge of regulatory documentation and SOPs.
• Experience coordinating clinical study activities across sites.

Responsibilities

• Execute feasibility, site activation, and maintenance activities per regulations and SOPs.
• Prepare and review site documents and contracts; manage site performance metrics.
• Serve as primary contact for investigative sites and track document completion.

Skills

Regulatory documentation

Project coordination

Education

Bachelor's degree in Life sciences or related field

Clinical research experience 1-3 years

Healthcare environment experience 3+ years

Job description

IQVIA is seeking a candidate to support feasibility, site activation, regulatory start-up, and ongoing maintenance activities at regional or country levels. The role involves preparing site documentation, reviewing contracts, and tracking performance metrics while ensuring all activities comply with regulations and SOPs.

Under moderate supervision, you will coordinate with the Project Management team and other departments, review regulatory and ethics approvals, and help establish timelines for