clinical documentation

Clinical Study Associate I Are you passionate about clinical research and interested in contributing to work that improves human health? If so, this opportunity may be a great fit for you. CellCarta is seeking an entry-level Clinical Study Associate (CSA I) to join our dynamic team in Wilrijk, Antwerp. As a leading clinical research organization, we are...

Paediatric Clinical Research Nurse The closing date is 24 June 2026. An exciting fixed‑term opportunity has arisen for a dynamic Band 6 Children's Clinical Research Nurse to join our inspirational Wolf CRF team. The successful candidate will support the delivery of high‑quality research and clinical care for children and young people across a range of...

Our client, a leading life sciences organization, is seeking a specialist to assess and enhance a quality management system in alignment with EU GMP requirements. The role supports inspection readiness and a manufacturing import authorization project to enable compliant processes for clinical product certification. Review and assess the current quality...

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...

Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCPAssist with or oversee study...

Change people's lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market‑leader in implantable hearing devices, more people choose a Cochlear‑branded cochlear implant system than any other. Our employees tell us that the number one reason they enjoy working for...

We are looking for a highly organised and proactive Clinical Trial Assistant (CTA) for a one year Fixed term role to join our Clinical Operations team in Belgium.In this role, you will provide essential administrative support for the planning, execution, and documentation of international clinical trials that contribute to the development of life-changing...

## Clinical Trial AssistantApply: Mechelen, Belgium: Full time: Posted Today: R-623976Change people’s lives and love what you do! Cochlear develops world-leading medical devices that help people hear. As a top 100 medical device company and market-leader in implantable hearing devices, more people choose a Cochlear-branded cochlear implant system...

Position Summary: The Senior Manager, Clinical Operations – Clinical Process Owner is responsible for leading the governance, harmonization, and continuous improvement of Clinical Operations processes across the organization. The role owns the development, simplification, alignment, and lifecycle management of Clinical Operations SOPs, work instructions,...

Senior Manager, Clinical Contracts – EMEAIn order to make an application, simply read through the following job description and make sure to attach relevant documents.Location: Brussels, BelgiumAdditional Location: Antwerp may be considered depending on candidate profileEmployment Type: Permanent, Full-TimeWorking Arrangement: Hybrid, with regular site...

📍 Location : Hybrid 🕓 Type : Full-time Do you want to protect the safety & well-being of subjects and guarantee data quality? Do you get energy from daily communication with investigators, study coordinators and study teams? Do GCP ICH E6 R2 and ISO 14155 have no secrets anymore for you? Do you like to perform monitoring visits in hospitals and want to...

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,...

Job Description For one of our clients, a medical device company based in the North of Brussels, we are looking for an enthusiastic Clinical Study Start-up Specialist to come on board and join the team to cover sites located in Flanders and in the Netherlands. This position is open for candidates with fluency in Dutch and English and a few years experience...

Senior Manager, Clinical Contracts – EMEAIn order to make an application, simply read through the following job description and make sure to attach relevant documents.Location: Brussels, BelgiumAdditional Location: Antwerp may be considered depending on candidate profileEmployment Type: Permanent, Full-TimeWorking Arrangement: Hybrid, with regular site...

Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study...

Serve as main CTI contact for assigned study sites Conduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCP Assist with or oversee study...

European Clinical Training & Demo Manager located at ORSI Academy, Belgium.Position OverviewWe are seeking an experienced and highly organised European Clinical Training & Demo Manager to lead and coordinate customer training and customer demonstrations at the ORSI Academy, in Belgium.The Clinical Surgical Robotics Trainer is responsible for delivering...

Eno Health is building an AI-powered clinical decision-support platform and is seeking a data-science lead to own the models, evaluation plans, and statistical rigour behind the knowledge graph. You will work with clinical, engineering and product teams to turn clinical knowledge into computable artefacts, with strict documentation, review, and...

pEno Health is building an AI-powered clinical decision-support platform and is seeking a data-science lead to own the models, evaluation plans, and statistical rigour behind the knowledge graph. /ppYou will work with clinical, engineering and product teams to turn clinical knowledge into computable artefacts, with strict documentation, review, and...