clinical study

Senior Manager, Clinical Contracts – EMEA Location: Brussels, Belgium Additional Location: Antwerp may be considered depending on candidate profile Employment Type: Permanent, Full-Time Working Arrangement: Hybrid, with regular site presence expected Travel: Some EMEA travel may be required Salary: Competitive, dependent on experience About the...

Agomab Therapeutics is seeking a Senior Clinical Trial Associate to provide high-quality administrative and operational support to the Clinical Operations Team in Antwerp. You will ensure timely, compliant execution of clinical trials, maintain TMF, and support trial logistics in a fast‑paced biotech setting.The role reports to the Head of Clinical...

Sr. Clinical Research Associate - Belgium (French & Dutch Fluency)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...

Job DescriptionAs 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 of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and...

JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand. This...

Amplity Health is seeking a Clinical Development Liaison for the Benelux region (Netherlands and Belgium) to support clinical development programs in neuromuscular diseases. This field-based, remote position involves investigator engagement, site activation, and patient recruitment across the Benelux region.You will collaborate with Medical Affairs, Clinical...

A clinical research organization in Belgium is looking for a full-time Supply Chain Specialist to join their team. The role involves preparing supply chain timelines, collaborating with vendors, and ensuring alignment with study requirements. Ideal candidates have a Bachelor's degree, 3-5 years of supply chain experience, and strong communication skills. The...

Cochlear is seeking a highly organized Clinical Trial Assistant (CTA) for a one-year fixed-term role in Belgium. You will support international clinical trials, coordinate documentation, and ensure compliance with GCP and ISO 14155.The role collaborates with CPMs, CRAs, sites, and partners across Europe and globally. The position emphasizes trial...

Cochlear Limited in Mechelen, Belgium is seeking a highly organized Clinical Trial Assistant for a one-year fixed-term role within the Clinical Operations team. You will support planning, execution and documentation of international clinical trials, coordinating with CPMs, CRAs, sites and external partners to ensure compliant, efficient study conduct.The...

IQVIA Biotech in Belgium is seeking a Clinical Research Associate to support Phase I–IV trials. You will conduct site evaluations, initiate visits, and monitor study progress in accordance with Good Clinical Practices, under the guidance of a CTM/Lead CRA.Based in Belgium, you will collaborate with investigators and internal teams, ensure data quality, and...

## Clinical Development Liaison (CLD) - Neuromuscular Diseases - BeneluxApply: Belgium: Netherlands: Full time: Posted Today: R6182Join Amplity, the full-service go-to partner of biopharma companies that delivers flexible + specialized medical + commercial services. No matter where a drug is in its lifecycle, we scale with ease to maximize...

BeOne in Belgium invites a Clinical Research Manager to lead trial monitoring staff remotely, ensuring study start-up and ongoing monitoring align with ICH/GCP and local regulations.The role requires 5–7 years in clinical operations in biotech/pharma, line management experience, oncology exposure preferred; fluency in German and local language is critical,...

Medpace in Belgium (Vlaams-Brabant) seeks Medical Directors to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. Serve as the internal medical expert for study design, protocols, and project plans. Responsibilities include medical management, safety oversight, and collaboration across...

About Cogstate At Cogstate, we’re advancing the science of brain health - making it faster, easier, and more accurate to assess cognition across clinical trials, healthcare settings, and everyday life. Our digital cognitive assessments are trusted by researchers, clinicians, and pharmaceutical partners around the world, helping to drive breakthroughs in...

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...

Our client, a global leader in the MedTech industry, is looking for a Senior Clinical Research Associate to support clinical study activities within a MedTech environment.The successful candidate will be responsible for managing clinical activities at study sites conducting clinical studies, while building strong and productive relationships with internal...

AbbVie is seeking a Clinical Research Associate (CRA) to support clinical studies in Belgium. You will partner with investigators and site teams to promote study delivery, data quality, and compliance. You will monitor sites, ensure patient safety, and help recruit and retain participants, while maintaining audit readiness.You will collaborate with the...

Medpace in Belgium (Vlaams-Brabant) seeks Medical Directors to provide medical, scientific, and strategic leadership for planning, execution, and reporting of clinical trials. Serve as the internal medical expert for study design, protocols, and project plans.Responsibilities include medical management, safety oversight, and collaboration across departments;...

CellCarta is seeking a Clinical Study Specialist I to ensure site-level regulatory documentation, monitoring visits, and close-out activities are executed with precision. You will liaise with Project Management, Regulatory Affairs, and QA to maintain audit readiness across oncology trials.The role requires 2+ years in clinical research, GCLP/GDP knowledge,...

Job Summary Medpace is currently seeking candidates with Radiopharmaceutical or Nuclear Medicine 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...