Clinical Research Coordinator

Clinical Research CoordinatorAs a clinical research coordinator, you will be responsible for the daily management and administration of clinical trials.You will ensure that all trial-related activities are conducted in compliance with Good Clinical Practice (GCP), applicable regulations, and standard operating procedures (SOPs).Additionally, you will...

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...

Senior Clinical Data Science Programmer - Remote - BrazilICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Senior Clinical...

Senior Clinical Data Science Programmer - Remote - Brazil ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior...

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...

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...

Job Description We are seeking a diligent and organized professional to serve as the operational partner for our founder. This key role involves ensuring focus, organization, and follow-through across daily and weekly priorities. Weekly & Daily Planning: Lead Monday check-ins to align priorities and manage task lists in Workflowy and Google Workspace....