Clinical Research Associate
il y a 2 semaines
Clinical Research Associate – Belgium (Home-Based / Hybrid) Chloe O'Shea is partnering with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking a Clinical Research Associate to join a dedicated single-sponsor team in Belgium. This is an exciting opportunity to take ownership of site responsibilities, strengthen your expertise, and accelerate your career in clinical research, all while enjoying the flexibility of a home-based or hybrid position. The Role As a CRA, you will be responsible for the successful management of clinical trial sites across Belgium. You will act as the primary point of contact for investigative sites, ensure compliance with study protocols, ICH-GCP, and local regulatory requirements, and manage all aspects of site monitoring. This role is ideal for CRAs who already have hands-on monitoring experience and are looking to further develop their career within a dedicated, supportive team. Key Responsibilities Independently manage site qualification, initiation, monitoring, and close-out visits. Ensure strict compliance with ICH-GCP, local regulations, and sponsor SOPs. Conduct source data verification, investigational product accountability, and maintain accurate site documentation. Build and maintain strong professional relationships with site staff and study teams. Proactively identify, resolve, and escalate site-level challenges to keep studies on track. Maintain complete and accurate trial documentation in CTMS, eTMF, and EDC systems. Requirements Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related field. 6–18 months of independent monitoring experience (CRO or pharmaceutical company). Knowledge of ICH-GCP and Belgian clinical trial regulations. Fluent in English and French, with basic Dutch. Strong communication, organizational, and relationship-management skills. Based in Belgium, with flexibility for home-based or hybrid working. What's in It for You? This role offers a competitive salary and benefits package, flexible working options, and the opportunity to take ownership of clinical trial sites while building a strong foundation for your clinical research career. You will gain experience working on meaningful studies, collaborate with an international team, and develop the expertise needed to progress quickly in the field. If you are a CRA with hands-on monitoring experience looking to take on real responsibility and grow your career, we'd love to hear from you. Apply today to join a global team dedicated to advancing clinical research and making a tangible impact.
-
Principle Clinical Research Associate
il y a 2 semaines
Laeken, Belgique AL Solutions Temps pleinSr/Principal Clinical Research Associate – Belgium (Home-Based / Hybrid, Cell & Gene Therapy) Chloe O'Shea is partnering with a leading global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking a Sr/Principal Clinical Research Associate with Cell and Gene Therapy experience to join a dedicated FSP team in...
-
Senior Clinical Research Associate
il y a 1 heure
Laeken, Belgique Planet Pharma Temps pleinSenior Clinical Research Associate Belgium | Remote | Permanent A global clinical research organisation is hiring a Senior Clinical Research Associate to support oncology clinical trials in Belgium This is a remote, permanent opportunity offering autonomy, responsibility, and involvement in complex, science-driven studies. The Role Lead site monitoring...
-
Clinical Research Associate
il y a 3 semaines
Laeken, Belgique Advanced Resource Managers Temps pleinTitle: Clinical Research Associate (FSP) Location: Belgium (remote) Salary: Up to €62,000 plus car allowance/company car and benefits My client is a top global CRO specialising in the completion of complex clinical trials and is a global leader in delivering comprehensive, integrated drug development services to the pharmaceutical, biotechnology, and...
-
Clinical Research Associate II
il y a 4 semaines
Laeken, Belgique Artivion EMEA Temps pleinIt's a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you...
-
Clinical Research Associate II
il y a 2 semaines
Laeken, Belgique Artivion EMEA Temps pleinIt’s a good feeling to know you're doing your best with purpose every day. At Artivion, we manufacture high-quality products and solutions for the treatment of aortic diseases. Together with surgeons worldwide, we save lives. In doing so, we rely on the strengths of each and every employee. Your strength counts, too: As an important link in the chain, you...
-
Senior Clinical Research Associate
il y a 2 semaines
Laeken, Belgique Planet Pharma Temps pleinTitle: Senior Clinical Research Associate Company: Global Leading CRO Location: Remote - Belgium Our client is seeking an experienced CRA II or Senior CRA with strong oncology experience to take full ownership of 1–2 clinical protocols. This role goes beyond traditional monitoring, encompassing contract negotiation, start-up activities, monitoring, and...
-
Senior Clinical Research Associate
il y a 2 semaines
Laeken, Belgique Planet Pharma Temps pleinPlanet Pharma are currently partnered with a global clinical research organisation and we are actively seeking a Senior CRA to join the business on a permanent basis, fully remotely in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted according to protocol, Good Clinical Practice (GCP), and regulatory requirements....
-
Clinical Trial Associate
il y a 2 semaines
Laeken, Belgique Planet Pharma Temps pleinAbout the Company A Global Pharmaceutical company About the Role The Clinical Trial Associate (CTA) provides essential operational support to the Global Clinical Project Management function, helping ensure clinical studies are delivered on schedule and in compliance with quality, regulatory, and procedural requirements. The role contributes to the planning,...
-
In-House CRA
il y a 3 semaines
Laeken, Belgique Oxford Global Resources Temps pleinFor one of our clients, a global Medical Device company we are looking for an In House-CRA, to support the Global Clinical Operations (GCO) Center of Excellence, driving technology enablement, process innovation, and clinical excellence across divisions. Job Description As a In House Clinical Research Associate (CRA) within our Global Clinical Operations...
-
Clinical Data Specialist
il y a 2 semaines
Laeken, Belgique R&D Partners Temps pleinJoin a growing Clinical Data Management team as a Clinical Data Specialist and help shape the future of data integrity in clinical research! R&D Partners is seeking a Clinical Data Specialist to join a leading organization who are continuously growing their Clinical Data Management function. Please note that to be considered for this role you must have the...
