Contract Clinical Research Associate

Senior Clinical Research Associate (CRA) — Epilepsy Study (Phase II/III)I’m currently looking for experiencedSenior CRAsto join an excitingPhase II/III Epilepsy Studywith one of my key clients. This is a1.0 FTE contract rolesupporting 6–8 sites across theCentral and Eastern U.S.— and it’s available for animmediate start .If you’re someone who...

About the RoleWe are seeking a skilled Freelance Clinical Research Associate (CRA) to support Phase 2 and 3 clinical trials.Key Responsibilities:Conduct site evaluations, initiations, monitoring & close-outsEvaluate compliance and ensure data integrityCollaborate with investigators and internal teamsReview protocols and study manualsSupport site staff with...

Join IQVIA Biotech as a Freelance CRA supporting Phase 2 and 3 clinical trials. You’ll lead site visits, monitor compliance, and ensure high-quality data—all while working with a passionate team.We currently have two projects in Brazil:Location: Brazil - travel required for both roles across BrazilHours: 1 x 0.35 FTE and 1 x 0.6 FTEStart: ASAPDuration: 6...

Responsible for the clinical operations of a project at the regional/global level. The Clinical Operations Lead oversees project deliverables, Clinical Research Associates (CRAs), and investigator sites in accordance with monitoring plans, protocols, Good Clinical Practice (GCP), ICH guidelines, and local regulations. The role serves as the primary liaison...

Contracts Manager page is loaded## Contracts Managerlocations: São Paulo, Braziltime type: Full timeposted on: Posted Todaytime left to apply: End Date: November 16, 2025 (26 days left to apply)job requisition id: R **Overview**As a Contracts Manager within the IQVIA US Contracting Center (USCC), you will review, draft and/or redline contracts within the...

Responsible for the clinical operations of a project at the regional/global level. The Clinical Operations Lead oversees project deliverables, Clinical Research Associates (CRAs), and investigator sites in accordance with monitoring plans, protocols, Good Clinical Practice (GCP), ICH guidelines, and local regulations. The role serves as the primary liaison...

Responsible for the clinical operations of a project at the regional/global level. The Clinical Operations Lead oversees project deliverables, Clinical Research Associates (CRAs), and investigator sites in accordance with monitoring plans, protocols, Good Clinical Practice (GCP), ICH guidelines, and local regulations. The role serves as the primary liaison...

The Site Contract Specialist will be responsible for the execution, negotiation and administration of assigned site contracts and supporting documents including, confidentiality agreements, clinical trial agreements, letters of indemnity and authorization. The incumbent will coordinate with sites, sponsors, vendors and internal stakeholders to facilitate the...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associate (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations. The COL acts as a primary liaison...

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.What You Will Be DoingCompletes onsite and...