Clinical Site Activation & Contract Negotiator

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

Job summary

IQVIA in Lexington, KY seeks a Site Activation Specialist to support feasibility, site activation, regulatory, and start-up activities at regional or country levels under moderate supervision. You will prepare and manage site documentation and coordinate with the SAM, Project Management, and other departments to ensure timely activation.

The role requires a Bachelor's in Life Sciences and 1–3 years of clinical research or healthcare experience, with responsibilities including contract review,

Qualifications

• 1-3 years clinical research or related experience.
• 3 years healthcare environment experience or equivalent.

Responsibilities

• With moderate oversight, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to regulations, SOPs and work instructions, working with SAM and Project Management.
• Prepare site documents, reviewing 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 information.
• Review, track and follow up progress, approval and execution of required documents (ICF, CDAs, regulatory/ethics approvals, IP release docs).

Skills

Clinical research experience

Healthcare environment experience

Education

Bachelor's Degree Life sciences

Job description

IQVIA in Lexington, KY seeks a Site Activation Specialist to support feasibility, site activation, regulatory, and start-up activities at regional or country levels under moderate supervision. You will prepare and manage site documentation and coordinate with the SAM, Project Management, and other departments to ensure timely activation.

The role requires a Bachelor's in Life Sciences and 1–3 years of clinical research or healthcare experience, with responsibilities including contract review,