clinical documentation

Freelance Senior Clinical Research AssociateFull-timePSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.As a Senior CRA, you will work on the...

Freelance Senior Clinical Research AssociateFull-timePSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.As a Senior CRA, you will work on the...

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...

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...

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the...

Mission Overview: We are seeking a Quality Specialist – Clinical QP for a consultancy mission at a client site, representing Keystone Solutions. In this role, you will assess and strengthen the Quality Management System (QMS) in alignment with applicable EU GMP requirements, supporting inspection readiness and the Manufacturing Import Authorization...

IQVIA LLC seeks an Associate Clinical Project Manager to lead Local Study Teams at the country level, ensuring delivery of study commitments within budget and timelines. You will coordinate site qualification, regulatory submissions, and master documents, while monitoring overall study progress and quality across the country.The role requires a life sciences...

CTI Clinical Trial and Consulting Services is seeking an experienced Clinical Research Associate to oversee monitoring activities at assigned study sites. The role includes site visits, regulatory document handling, and collaboration with sponsors and project teams to ensure quality and timelines.You will contribute to study start-up, patient enrollment...

The Franchise Clinical Operations Development Lead (CODL) is responsible for the strategizing, planning, leading and execution of the operational path for all indications within a franchise from first in human studies through authorization and commercialization. The franchise may involve several assets and/or may cover specific development phases across all...

The Clinical Trial Manager is responsible for overseeing all clinical operational aspects of assigned global clinical studies from planning through to study closure. This includes coordination of internal and external stakeholders, ensuring quality standards, and adherence to timelines and budget.Main activities are:Actively participates in clinical trial...

🔍 Quality Manager Clinical 📍 Location : Remote - Europe 🕓 Type : Full-time The Quality Manager is responsible for the development, implementation, maintenance, and continuous improvement of QbD Group’s Quality Management System (QMS), ensuring its alignment with applicable international standards – such as GCP, ISO 9001, ISO 13485 and other GxP...

The Entry Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a...

Excelya is seeking a highly organized clinical operations professional to coordinate trials across sites and countries, ensuring regulatory compliance and timely execution.You will manage TMF, trial documentation, study systems, and cross-functional communication, contributing to a high-quality patient journey. This role offers exposure to global studies and...

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...

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...

Job Summary The Entry Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field and be...

Jobtailor in Belgium is seeking a Clinical Operations Assistant to support monitoring activities, maintain the Trial Master File (TMF) and project files, and assist with site management tasks. You will coordinate documentation, prepare site manuals and reference tools, manage incoming and outgoing regulatory documents, and support team meetings to ensure...

European Clinical Training & Demo Manager located at ORSI Academy, Belgium.Applying for this role is straight forward Scroll down and click on Apply to be considered for this position.Position OverviewWe are seeking an experienced and highly organised European Clinical Training & Demo Manager to lead and coordinate customer training and customer...

Capgemini Engineering in Belgium is seeking a Logistics Specialist to own end-to-end clinical supply chain activities within a regulated pharmaceutical environment. You will coordinate shipments, warehousing, and documentation while collaborating with a small, dedicated team to ensure compliant, timely distribution globally.Ideal candidates have 3–5 years...