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 Brazil — and it's available for animmediate start.If you're someone who thrives in neurology studies...

**Company Description**PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.As a Clinical Research Associate at PSI you will enjoy a...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate Job Overview Monitoring clinical studies in phases II-III...

Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate II (CRA II) / Sr. Clinical Research Associate (Sr. CRA) to join our A-team (remote; with travel). As a CRA at Allucent, you will independently control and monitor investigational sites, pro‑actively detect issues, provide solutions to ensure...

**In Parexel we are looking for experienced CRA to make onsite monitoring visits in Brazil.****Oncology experience is required.****Your time here**At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure...

**Parexel FSP is hiring multiple Sr CRAs in Brazil!** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the...

**Parexel FSP is hiring multiple Sr CRAs in Brazil!**The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the...

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 site sponsors, vendors, and internal stakeholders to facilitate the...

As a Regulatory Affairs Associate at Parexel Consulting, you will support clinical trial submissions to regulatory authorities, focusing on projects in Brazil. This role offers an opportunity to develop skills in regulatory affairs and clinical research while working with experienced professionals.**Key Responsibilities**:- Contribute to high-quality...

Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do.**Job Title**Clinical Operations SpecialistAt Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life- changing medicines to patients. We are seeking Clinical...