clinical trial coordinator- fsp

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.We have a vacancy for...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.We have a vacancy for...

A leading clinical trials organization is seeking a full-time Project Coordinator in Leuven, Belgium. The role involves maintaining study-related documents, coordinating laboratory shipments, and serving as a primary contact for study teams. Ideal candidates should hold a Bachelor's degree in life sciences and demonstrate excellent organizational and...

UZ Leuven zoekt een clinical trial assistant binnen radiotherapie-oncologie om klinisch onderzoek te versterken en patiënten zorgzaam te begeleiden. Je werkt zelfstandig in nieuwe studies, controleert gegevens en toetst deelname aan studies volgens protocollen.Je biedt planning-ondersteuning voor consultaties en follow-up, voert technische metingen uit en...

Thermo Fisher Scientific is seeking a Clinical Trial Coordinator in Belgium to provide administrative and technical support to the Project Team. You will coordinate trial activities, maintain study documentation, and support onboarding and process improvements.Required: high school diploma, 4+ years’ experience, and strong Dutch/English skills. Proficiency...

Delta Healthcare Consulting zoekt in Willebroek een clinical trial assistant om als administratieve spil te fungeren voor lopende klinische studies. Je beheert administratieve taken en voorraden en fungeert als contactpunt voor de planning van deelnemers.Onze ideale kandidaat heeft minimaal 2 jaar ervaring in klinische studies, beschikt over een ICH-GCP...

Senior Clinical Trial 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 that...

Senior Clinical Trial 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...

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 Clinical Trial...

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

Medpace is seeking Infectious Disease PhDs and/or Post-Doctoral researchers for a full-time, office-based Associate Clinical Trial Manager to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers on clinical trial management activities.This role offers solid foundational training, an international...

A clinical contract research organization is seeking an Associate Clinical Trial Manager based in Belgium. This full-time position is ideal for recent PhD graduates looking to start their career in clinical trial management. You will work closely with project coordinators and clinical trial managers, ensuring effective communication and delivery of study...

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 SummaryMedpace is currently seeking candidates with Oncology related PhDs and/or Post-Doctoral Research experiencefor a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Belgium, Leuven Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical...

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...

Medpace in Leuven, Belgium is seeking an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team on a full-time, office-based basis. The role involves supporting global study activities alongside Project Coordinators and Clinical Trial Managers, applying analytical and academic skills to clinical project administration and...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.We have a vacancy for...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed...

Clinical monitoring 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 that benefit...

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...