Site Activation & Contract Negotiator

IQVIA Argentina; Durham (NC); On-site; USD 49,000 - 123,000; Full time

Job summary

IQVIA seeks a responsible professional to support feasibility, site activation, regulatory start‑up and maintenance activities across studies. You will coordinate site documentation and timelines under supervision to ensure compliant execution.

Primary responsibilities include managing documents, tracking regulatory approvals, and collaborating with sponsors and sites to maintain project performance metrics.

Qualifications

• Bachelor's Degree in Life Sciences or related field required.
• 1-3 years clinical research or relevant experience.
• 3 years healthcare experience preferred.

Responsibilities

• Perform feasibility, site activation and some maintenance in studies with guidance.
• Prepare site documents for regulatory and contractual purposes.
• Inform team on completion of regulatory, contractual and other documents.
• Update internal systems and project timelines with accurate data.
• Review and track documents like CDAs, ethics approvals, IP release docs.

Skills

Site activation

Clinical research

Regulatory knowledge

Education

Bachelor's Degree Life sciences

Job description

IQVIA seeks a responsible professional to support feasibility, site activation, regulatory start‑up and maintenance activities across studies. You will coordinate site documentation and timelines under supervision to ensure compliant execution.

Primary responsibilities include managing documents, tracking regulatory approvals, and collaborating with sponsors and sites to maintain project performance metrics.