Senior Clinical 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...

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...

For our client, a global medical device company, we are looking for a Clinical Research Associate.Position SummaryThe Clinical Research Associate (CRA) is responsible for monitoring and overseeing clinical investigations involving medical devices to ensure compliance with applicable regulations, Good Clinical Practice (GCP), study protocols, and company...

As a Clinical Research Associate, you will be responsible for managing clinical study activities across multiple study sites within one or more clinical projects for the MedTech group. You will play a key role in ensuring the successful execution of clinical trials, maintaining high-quality data collection, and safeguarding the safety and well-being of study...

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...

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...

For our client, a global medical device company, we are looking for a Clinical Research Associate. Position Summary The Clinical Research Associate (CRA) is responsible for monitoring and overseeing clinical investigations involving medical devices to ensure compliance with applicable regulations, Good Clinical Practice (GCP), study protocols, and company...

IQVIA Belgium invites a Clinical Research Associate to join our Site Management team. You will monitor sites, ensure protocol adherence, and help drive data quality and regulatory compliance across studies.We seek a university graduate with CRA experience, fluent Dutch, French, and English, and readiness to travel within Belgium. You will collaborate with...

Progressive in Belgium is seeking a Clinical Research Associate to manage study activities across multiple sites for MedTech projects. You will ensure high-quality data collection, safeguard participant safety, and act as liaison between clinical teams and site personnel.The role requires collaboration with investigators, vendors, and internal stakeholders,...