clinical study assistant

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Sr. Clinical Data Manager (SrCDM) to join our A-team (hybrid*/remote). As a SrCDM at Allucent you lead data management...

For the expansion of our Global Clinical Trial Operations team, argenx is looking for a Clinical Operations Development Lead.Key Accountabilities/Responsibilities:The Clinical Operations Development Lead (CODL) is responsible for the oversight of the clinical related activities within a specific therapeutic indication for an asset (CODL) or across all...

Make your mark for patientsHead of Clinical StandardsYou will be working in a team that is shaping the future of modern, digital, data‑driven research and development. We are looking for a Head of Clinical Standards who is strategic, collaborative, and forward‑thinking to join us in our Research and Development team, based in our UCB office in Brussels,...

A leading clinical research organization is seeking an Associate Clinical Trial Manager in Leuven, Belgium. This full-time role requires a PhD in Life Sciences and offers intensive training for recent graduates looking to develop their careers in clinical trial management. Responsibilities include collaboration on global study activities, maintaining...

ICON Strategic Solutions is seeking a Senior Clinical Trial Manager to oversee clinical trial operations and support the team and stakeholders across programmes. You will focus on coordinating delivery, resolving issues, and building team capability.The role includes budget oversight, monitoring plan development, CRA mentoring, and driving study start-up and...

Van studiedata tot patiëntencontact: als clinical trial assistant ben je een onmisbare schakel binnen klinisch onderzoek Verleg Grenzen Als Clinical Trial Assistant Binnen Radiotherapie-oncologie De afdeling radiotherapie-oncologie van UZ Leuven is één van de grootste radiotherapieafdelingen van België. Dankzij moderne bestralingstoestellen en...

Labcorp is seeking a remote Clinical Data Risk & Solutions Analyst (Global Monitor) to join our Belgium-based team. The role involves managing a portfolio of studies, identifying risks, developing mitigation plans and writing monitoring instructions for study oversight.You will ensure study health and compliance with the Global Project Management strategy....

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...

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...

Snr CRA - Clinical Site Management At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments...

Lakefront Biotherapeutics is a global biotech with offices in Belgium, Chicago and San Francisco, focused on building a differentiated immunology and inflammation pipeline to address serious diseases with high unmet medical need. Our pipeline is anchored by T‑cell engager programs, led by a potential first‑in‑class clinical asset and complemented by an...

Senior Clinical Research Associate - Belgium About the Employer Chloe O'Shea has partnered with a small, specialist clinical CRO providing tailored clinical research services across Belgium and the Benelux region. The organization offers a collaborative, quality-focused environment where employees have the opportunity to take on meaningful responsibilities...

Job description Join Amaris Consulting and support one of our leading clients in the successful delivery of clinical studies within an international and highly regulated environment. Your responsibilities Lead and coordinate clinical projects from study start-up through close-out. Develop and monitor project timelines, budgets, resources and key...

JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand.We are seeking a Clinical Outcome Assessment (COA) Lead to drive COA strategy across innovative clinical development programs, ensuring the patient voice is integrated into...

We are looking for a driven Manager Clinical Operations to join our growing Clinical Operations team in Belgium (Beerse) and The Netherlands (Breda). As a Clinical Research Manager, you will manage a team of Local Trial Managers (Local project managers), Site Managers (Clinical Research Associates) and Clinical Trial Assistants, with a strong focus on staff...

Medpace is seeking a Site Contract Manager to join our Clinical Operations team in Belgium. You will oversee end-to-end CTA processes for global, multi-site trials and develop study-specific CTA strategies with Sponsors and internal stakeholders. The role requires a Bachelor’s degree in a relevant field, CRO experience, and strong negotiation, leadership,...

Alimentiv is seeking an experienced Clinical Research Associate to independently perform and oversee site monitoring for multi-site studies in Belgium. You will ensure protocol and regulatory compliance, act as liaison between sponsor and investigative sites, and mentor CRA I/II colleagues.The role includes CRA Assessment Visits, audits/inspections, and...

Pauwels Consulting seeks a Clinical Research Associate to oversee clinical activities across study sites for medical device projects. You will monitor sites, ensure data quality, and manage regulatory compliance with GCP and SOPs. Travel up to 80% to investigator sites is required.Fluency in English and Dutch, a life sciences degree, and 2+ years in clinical...

Medpace is seeking a Site Contract Manager to join our Clinical Operations team in Belgium. You will oversee end-to-end CTA processes for global, multi-site trials and develop study-specific CTA strategies with Sponsors and internal stakeholders.The role requires a Bachelor’s degree in a relevant field, CRO experience, and strong negotiation, leadership,...

Abbott in Belgium seeks an EP Field Clinical Specialist to support clinical research across Europe. This field-based role collaborates with clinical sites, physicians, and study teams, traveling up to 75% during active trials to ensure patient safety and high-quality study execution.The position is remote within Europe, requiring 2–3 years in...