Senior Clinical Research Associate

CTI Clinical Trial and Consulting Services is seeking an experienced Clinical Research Associate to oversee monitoring activities at assigned study sites. The role includes site visits, regulatory document handling, and collaboration with sponsors and project teams to ensure quality and timelines.You will contribute to study start-up, patient enrollment...

Freelance Senior Clinical Research AssociateFull-timePSI is a leading Contract Research Organisation with 30 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 Senior CRA, you will work on the...

Freelance Senior Clinical Research AssociateFull-timePSI is a leading Contract Research Organisation with 30 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 Senior CRA, you will work on the...

Alimentiv independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between sponsor/Alimentiv and investigative sites by playing a critical...

PSI CRO is seeking a Freelance Senior Clinical Research Associate in Belgium to lead on-site monitoring, ensure data quality and compliance, and maintain timely study milestones.You will manage site communications, perform source data verification, support vendors, and coordinate monitoring visits across Phase II/III oncology, hematology, and infectious...

EPM Scientific are currently partnered with a leading Medical Device organisation conducting international clinical research programmes across Europe. They are seeking a Clinical Research Associate to support ongoing and upcoming clinical studies. This individual will play a critical role in overseeing clinical study sites, ensuring high-quality data...

Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCPAssist with or oversee study...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of...

Clinical Research AssociateIQVIA Belgium is looking for talented and motivated CRA to join our Site Management team. At this position you will have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas, and build a meaningful, strong career within our organization.Perform...