clinical study

Senior Clinical Research Associate (F/M/X) Permanent Job As a Senior Clinical Research Associate, you will be responsible for managing clinical activities and ensuring the successful execution of clinical studies, particularly in the field of cardiac electrophysiology. Your missions Manage clinical study activities for multiple sites across single or...

Telix Pharmaceuticals Limited is seeking a Clinical Project Manager to lead day-to-day responsibilities of multiple early‑phase regional trials from protocol conception through the study report, ensuring GCP compliance, quality data, and on‑budget delivery.The CPM will partner with CROs and vendors, coordinate cross-functional teams, and drive risk...

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...

Clinical Research AssociateFor candidates able to start before December 2026, a discretionary sign‑on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team CRA (Junior - Senior)...

## 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...

Thermo Fisher Scientific is seeking an Associate Medical Director to provide medical support and safety assessment for clinical trials within the PPD Pharmacovigilance department. You will lead study teams, review protocols, and ensure medical validity of endpoints while safeguarding patient safety.You will collaborate with investigators, IRBs, and health...

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...

Alimentiv is seeking an experienced CRA leader to independently perform and oversee clinical site monitoring, ensuring protocol and regulatory compliance across ICH‑GCP standards. You will mentor CRA I/II and collaborate with cross‑functional teams, while coordinating audits and site initiation efforts.The role requires up to 40–60% travel, strong data...

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 the sponsor/Alimentiv and investigative sites by playing a critical role in...

Questa posizione è in IQVIAIl processo di selezione sarà interamente gestito IQVIA.Questa opportunità è disponibile in Reading - United Kingdom, Belgrade - Serbia, Budapest - Hungary, Barcelona - Spain, Berlin - Germany, Sofia - Bulgaria, Bellville - South Africa, Bucuresti - Romania, Milan - Italy, Madrid - Spain, Lisbon - Portugal, Brussels - Belgium,...

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...

JoinExcelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. This role combines operational excellence, clinical trial coordination, and regulatory compliance, playing a key role in ensuring the seamless...

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 the sponsor/Alimentiv and investigative sites by playing a critical role in...

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 the sponsor/Alimentiv and investigative sites by playing a critical role in...

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 the sponsor/Alimentiv and investigative sites by playing a critical role in...

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 the sponsor/Alimentiv and investigative sites by playing a critical role in...

4G Clinical is seeking a Backend Software Engineer to advance our Python/Django backend, focusing on safe, scalable solutions for clinical trial data and workflows. You will implement study-specific reports, data scripts, and client integrations with external APIs.The role requires 5+ years in a related field, strong communication, and willingness to travel...

Job Summary Medpace is currently seeking candidates with Infectious Disease PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers...

JOB SUMMARY• The Senior Manager, PCRU Clinical Systems Integration & Governance serves as the senior professional-track authority for technical integration governance, technology lifecycle oversight and operational reliability of PCRU clinical technology platforms, connected devices and supporting technical environments across the Brussels and New Haven...

Our client, a leading pharmaceutical organization, is seeking a professional to join their Manufacturing Science & Technology team. This role is responsible for the technical setup of kit designs and the end-to-end coordination of packaging and labeling requirements for global clinical studies.Coordinate the technical setup of clinical kit designs, including...