Epilepsy Study Clinical Lead

Senior Clinical Research Associate Opportunity We are seeking a highly experienced Senior Clinical Research Associate to join our team for an exciting Epilepsy Study (Phase II/III). This is a 1.0 FTE contract role, supporting 6–8 sites across Brazil and requires an immediate start. Key Responsibilities: Conduct regular site visits across Brazil to monitor...

Job Title: Clinical Research Associate As a diligent and experienced Clinical Research Associate, you will oversee the execution of Phase 2 clinical trials ensuring compliance with regulatory standards, Good Clinical Practice (GCP), and study protocol. Collaborate with investigators, site personnel, and cross-functional teams to guarantee participant safety...

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...

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...

Clinical Data Science Programmer Job Summary We're seeking a Clinical Data Science Programmer to develop and implement programming solutions supporting clinical trial data analysis and reporting. This role contributes to advancing innovative treatments and therapies by ensuring data accuracy and efficiency through expert programming.

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...

Clinical Research Coordinator As 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...

Clinical Project Manager Job Description As a senior project manager, you will be responsible for overseeing clinical projects across regions. Your expertise in regulatory compliance and project management will ensure that projects are completed within scope, time, and budget. Ensure strict adherence to regulatory guidelines and protocols. Develop and...

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...