research associate

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...

Within a Novalix insourcing team based in a pharmaceutical company, you will play a key role in the synthesis of complex molecules to support drug discovery programs. This position is offered as a 6-month fixed-term contract to support ongoing project activities. You will join a dynamic and highly motivated team, committed to exploring innovative synthetic...

Company DescriptionPSI 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.Job DescriptionAs a Senior CRA, you will work on the frontline of...

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries. Our...

Serve as main CTI contact for assigned study sites Conduct 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 GCP Assist with or oversee study...

Serve as main CTI contact for assigned study sites Conduct 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 GCP Assist with or oversee study...

Take the next step in your clinical research career and contribute to high quality clinical studies within the medical device sector. We are looking for 2 profiles:Like the look of this opportunity Make sure to apply fast, as a high volume of applications is expected Scroll down to read the complete job description.a Clinical Research Associate who combines...

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...

Within a Novalix insourcing team based in a pharmaceutical company, you will play a key role in the synthesis of complex molecules to support drug discovery programs. This position is offered as a 6-month fixed-term contract to support ongoing project activities. You will join a dynamic and highly motivated team, committed to exploring innovative synthetic...

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...

IQVIA Belgium is seeking a Clinical Research Associate to perform monitoring and site management, ensuring compliance with study protocols. The role involves conducting site visits, recruiting subjects, and maintaining communication with study sites.The ideal candidate holds a relevant degree and has at least 2 years of CRA experience. Strong organizational...

IQVIA Belgium is seeking a Clinical Research Associate (Junior–Senior) to join our Sponsor dedicated team. You will gain experience across therapeutic areas and build a meaningful career within our organization.Based in Belgium, you will perform site visits, support recruitment planning, and ensure regulatory compliance with GCP/ICH guidelines. You will...

Pauwels Consulting seeks a Senior Clinical Research Associate to manage clinical study activities across multiple sites in the MedTech field. You will oversee site performance, conduct monitoring visits, and ensure high-quality data collection for diverse medical device projects.This role requires a life sciences or nursing degree, 4+ years of site...

## Experienced Clinical Research Associate, Multi-Sponsor, BelgiumApplylocations: Brussels, Brussels-Capital Region, Belgiumtime type: Full timeposted on: Posted Todayjob requisition id: R1552876***Clinical Research Associate***IQVIA Belgium is looking for talented and motivated experienced CRA to join our Site Management team. At this position you...

Amaris Consulting is seeking a Clinical Research Associate to manage clinical activities across sites, focusing on cardiac electrophysiology. You will ensure data quality, regulatory compliance, and successful study execution. You will liaise with investigators, IRBs/ECs, vendors, and internal teams, while traveling up to 80% of the time.Dutch and English...

Oxford Global Resources is seeking an experienced Senior CRA for a freelance, full-time project starting asap in Belgium. You will monitor clinical sites, manage timelines, and ensure data quality while working remotely with on-site visits.You will lead onsite monitoring, perform CRF reviews, and cooperate with vendors, investigators and internal teams;...

Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites, pro-actively detect issues, and ensure studies are conducted per protocol, SOPs, and GCP/ICH guidelines.You will lead monitoring activities, manage site relationships, and support startup activities, including contracting. Travel is required across Belgium...

Are you an experienced freelance CRA and have full-time availability for a project to start asap? You will be welcomed in a global company in which team spirit is key. Job Description As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety...

PSI 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. PSI is a leading Contract Research Organisation with 30 years in the industry, offering a...

PSI CRO Belgium is seeking a Senior Clinical Research Associate (CRA) on a freelance basis to support on-site monitoring across Phase II/III studies. You will manage site relationships, ensure data integrity, and drive timelines and quality standards in collaboration with project teams.You will conduct on-site monitoring visits, perform CRF reviews, source...