clinical documentation

Senior Clinical Research Associate - BelgiumAbout the EmployerChloe 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 and...

This role as quality specialist – Clinical QP needs to assess and strengthen the Quality Management System in alignment with applicable EU GMP requirements. The function supports inspection readiness and the Manufacturing Import Authorization project by identifying gaps, defining actins, and enabling compliant processes for clinical product...

This role as quality specialist – Clinical QP needs to assess and strengthen the Quality Management System in alignment with applicable EU GMP requirements. The function supports inspection readiness and the Manufacturing Import Authorization project by identifying gaps, defining actins, and enabling compliant processes for clinical product...

Senior Clinical Research Associate - Belgium Check out the role overview below If you are confident you have got the right skills and experience, apply today.About the EmployerChloe 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...

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...

The Clinical Operations Development Lead (CODL) is a key member of the Indication Development Team (IDT), overseeing clinical activities for a specific therapeutic indication (CODL) or across all indications for an asset (early/late phase CODL). The CODL provides operational input and drives strategy for clinical development across the lifecycle of an asset,...

EPM Scientific are currently partnered with a leading Medical Device organisation conducting international clinical research programmes across Europe. They are seeking a Clinical Research Associate to support ongoing and upcoming clinical studies. This individual will play a critical role in overseeing clinical study sites, ensuring high-quality data...

Senior Clinical Trial AssociateDepartment: Clinical DevelopmentEmployment Type: Permanent - Full TimeLocation: Agomab AntwerpDescriptionThe Senior Clinical Trial Associate (CTA) is providing high-quality administrative and operational support to the Clinical Operations Team. In this role, you will report to the Head of Clinical Operations. You will play a...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards. As a...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards. As a...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards. As a...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards.As a key...

📍 Location : Hybrid 🕓 Type : Full-time Do you get energy from coordinating dynamic clinical trials with a quality-driven and pragmatic approach? Do you like to partner with many stakeholders? Do GCP ICH E6 R3 and ISO 14155 have no secrets anymore for you? You might be the Clinical Project Manager we are looking for at QbD Clinical! 🏢 What you’ll...

Our client, a leading player in the MedTech industry, is seeking a Senior Clinical Research Associate to manage clinical study activities across multiple sites. This role focuses on overseeing study site performance, conducting comprehensive monitoring visits, and ensuring high-quality data collection for various medical device...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards.Is this...

We are looking for an experienced Senior Clinical Research Associate (CRA) to support clinical studies within a dynamic MedTech environment. In this role, you will be responsible for managing and monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and quality standards.Is this...

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...

📍 Location : Hybrid 🕓 Type : Full-time We are seeking a dynamic and experienced Expert in Clinical Performance Studies to join our team, specializing in In Vitro Diagnostics (IVD). In this role, you will be designing, executing, and overseeing clinical performance studies for in vitro diagnostic (IVD) products. You will be ensuring that clinical...

Job Description Summary As part of the Clinical Education team, you will play a key role in supporting healthcare professionals in the effective clinical use of GE HealthCare's Computed Tomography (CT) solutions. As the clinical expert for your modality, you will deliver clinical education, application training, and ongoing customer support to ensure optimal...

This role as quality specialist – Clinical QP needs to assess and strengthen the Quality Management System in alignment with applicable EU GMP requirements. The function supports inspection readiness and the Manufacturing Import Authorization project by identifying gaps, defining actins, and enabling compliant processes for clinical product...