cras

Avida vzw is een dienstverlenend netwerk binnen de zorg voor ouderen en personen met een beperking dat bestaat uit negen wooncentra waarvan woonzorgcentrum Avida | Ter Hovingen er één is.Avida vzw staat voor wonen en leven ondersteund door warme en gedreven mensen.De vzw omarmt de eigenheid van de wooncentra en ondersteunende diensten, die elk op hun eigen...

Senior CRA position - single sponsorSyneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of InnovationWe 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...

CTI Clinical Trial and Consulting Services is seeking a Clinical Research Associate to monitor trials, manage site visits, and drive start-up activities. You will ensure regulatory compliance, oversee IP/material handling, and collaborate across sponsor and project teams.The role requires 3+ years in clinical trial monitoring, a relevant degree, and strong...

Oxford Global Resources in Brussels is seeking a Clinical Research Associate to monitor clinical investigations of medical devices ensuring GCP, ISO 14155, MDR compliance and data integrity.The CRA will perform site qualification, initiation, monitoring, and close-out visits, manage queries, review CRFs, and support audits, with up to 80% travel and onsite...

IQVIA Biotech in Belgium is seeking an experienced Clinical Research Associate to join the EU Clinical Monitoring team. You will participate in Phase I-IV trials, perform site evaluations, initiation visits, and ongoing monitoring in line with GCP/ICH.The role requires 1-2 years of on-site monitoring, strong communication skills in Dutch and English, and the...

EPM Scientific, partnered with a leading Medical Device organisation in Europe, is seeking a Clinical Research Associate to oversee clinical study sites and ensure high-quality data collection. You will monitor sites, ensure regulatory compliance, and support patient recruitment while traveling up to 80% across assigned sites.Start date Jan 2027; 12-month...

UZ Brussel: Samen sterk in zorg, innovatie en wetenschap  Word onze nieuwe collega binnen het clinical Trial center. Bij UZ Brussel bouwen we elke dag aan de zorg van morgen. Met bijna 5.000 collega’s zetten we ons in voor kwaliteitsvolle, innovatieve én warme patiëntenzorg. Als universitair ziekenhuis combineren we zorg, wetenschap en opleiding —...

Rhox in Brussels is seeking a Senior Security Compliance Officer to build and maintain an auditable cybersecurity compliance framework across NIS2, PCI DSS and the Cyber Resilience Act. The role emphasizes defining measurable controls and evidence rather than operational execution, with a focus on governance, risk assessment and continuous improvement.You...

Als CRA draag je actief bij aan de kwaliteit van zorg en leven van onze bewoners. Je adviseert over het medische zorgbeleid, stimuleert samenwerking en helpt ons om de medische werking verder te ontwikkelen en te optimaliseren.Je staat onder andere in voor:Meedenken over en adviseren rond het medische zorgbeleid.Overleg organiseren en samenwerking stimuleren...

CTI Clinical Trial and Consulting Services is seeking a seasoned clinical trial monitor to lead monitoring activities across assigned sites. You will ensure regulatory compliance, manage source data verification, and collaborate with cross-functional teams to drive trial quality and timelines.The role includes site visits (PSV, SIV, IMV, COV), start-up...

Amaris Consulting is recruiting a Senior Clinical Research Associate to manage clinical activities in cardiac electrophysiology across multiple sites. You will oversee site performance, ensure data quality, and liaise between the study team and site personnel.You will ensure patient safety, support trial execution, and comply with SOPs and regulatory...

PSI is a leading Contract Research Organisation seeking a Senior Freelance Clinical Research Associate in Belgium. You will lead onsite monitoring visits, review CRFs, and ensure data quality while maintaining strong site relationships and study timelines.Fluency in Dutch and English, proficiency in French, and willingness to travel are required, along with...

Arcadis is seeking an experienced Senior Clinical Research Associate to support and monitor clinical studies within a MedTech environment. You will manage multiple study sites, ensure protocol and GCP compliance, and drive data quality and study performance.Applicants should have 4+ years of site monitoring experience, strong communication skills, and...

Arcadis is seeking a motivated Clinical Research Associate (CRA) to oversee clinical study sites within a MedTech environment. You will monitor trial activities, ensure GCP compliance, and partner with investigators and operational teams to drive quality data and study delivery.Requirements include a Life Sciences degree (Bachelor/Master), 1–2 years of...

Don't see an opening that quite matches what you're looking for, or not ready to make a move yet? Let us know! We are proactively inviting qualified candidates to join our talent pool for anticipated Clinical Research Associate needs (across multiple seniority levels) to support our Clinical Monitoring team. What the Process Looks Like A Talent Acquisition...

Alimentiv is seeking an experienced CRA to independently perform and oversee all aspects of site monitoring, coordinating with sponsor sites and cross-functional teams in a high accountability environment. The role includes mentoring junior CRAs, conducting assessments and audits, and ensuring protocol and regulatory compliance in accordance with...

Medpace Overview Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical...

IQVIA Belgium is seeking a motivated Clinical Research Associate II to join our sponsor-dedicated model in Belgium, home-based.You will perform site monitoring visits per GCP/ICH, support recruitment plans, manage TMF documentation, and collaborate with cross-functional teams to ensure project success. The role requires a university degree in a scientific...

Alimentiv is seeking an experienced CRA to independently perform, coordinate and oversee site monitoring activities across clinical studies. The role ensures protocol and regulatory compliance and acts as a liaison between sponsor, Alimentiv, and investigative sites.The position involves mentoring CRA I and II, participating in audits, and aiding with site...