Clinical Research Coordinator

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: ******** FTE and 1 x 0.6 FTEStart: ASAPDuration: 6...

Job Title: Freelance Clinical Research AssociateWe are seeking a skilled Clinical Research Associate to support our global trials team.This is an excellent opportunity for those who want to work independently and manage multiple priorities while ensuring high-quality data.Our ideal candidate will have at least 2 years of experience in CRA, including site...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associates (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...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associates (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...

Responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research Associates (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...

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...

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...

Overview Job Title: Generative AI Associate Analyst (LLM Training – Medical Domain)Location: RemoteEmployment Type: Flexible Contract Role (Part‑time, up to 25 hours weekly) We are seeking highly qualified professionals with a Master’s or PhD in Medical Microbiology to support the development of state‑of‑the‑art Large Language Models (LLMs). As...

Overview The MainStreet Family Care Preceptorship Program is designed to provide aspiring healthcare professionals, specifically physician assistants, with hands-on experience and mentorship in a dynamic urgent care setting. This program aims to bridge the gap between academic knowledge and practical clinical skills, preparing individuals for successful...

We have partnered with our client in their search for a UX Designer – Reporting & Analytics in Brazil to work remotely. Responsibilities As a UX Designer, you will work inside a matrixed organization leading the design strategy, discovery, and delivery of reporting and analytics solutions for our Clinical Solutions products. You will work alongside a...