cmed clinical research services

The Institute of Tropical Medicine (ITM) in Antwerp is a leading independent academic centre for research, education and clinical services in the fields of tropical medicine and global health.Would you like to contribute to clinical research on infectious diseases as a nurse? At our Clinical Trial Site (CTS), you will combine nursing care with the conduct of...

Job Description As a Clinical Research Nurse, you will be part of the Clinical Trial Site (CTS), working closely with study physicians, nurses, researchers and support services. You will combine nursing care and direct contact with study participants with laboratory and administrative tasks. You will work within a team where the study coordinator helps...

Job Description :The Clinical Research Manager defines and owns the clinical evidence strategy for new and updated AI and machine learning algorithms within software‑based digital dentistry solutions. The role ensures that clinical intended use, clinical benefit, and performance claims are clinically and scientifically justified, competitively positioned,...

Clinical Research Coordinator in Turnhout Antwerp, Antwerp, Belgium Part time R1577435 Working Hours: 8-10 hours per week Start Date : Immediately Duration : Approximately 9 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Turnhout. This 8-10 hour per week role offers a unique opportunity...

Clinical Research Coordinator in TurnhoutWorking Hours: 8-10 hours per weekStart Date: ImmediatelyDuration: Approximately 9 monthsIQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Turnhout. This 8-10 hour per week role offers a unique opportunity to contribute to meaningful research in a...

Job Description Inhouse Clinical Research Associate (IHCRA) The Inhouse Clinical Research Associate (IHCRA) provides in-house support to the clinical team according to project requirements, ICH GCP guidelines, local or global regulatory requirements and Novotech or Client SOPs. Responsibilities RESPONSIBILITIES • Support the clinical team’s inhouse...

About Us Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition,...

About Us Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, we are proud to combine our position at the forefront of the industry with an award-winning workplace culture that values ambition,...

Clinical Research Coordinator in TurnhoutWorking Hours: 8-10 hours per week Start Date: Immediately Duration: Approximately 9 monthsKey ResponsibilitiesPrescreening and Screening tasksReview charts from the site data baseMaintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and...

Clinical Research Coordinator in TurnhoutWorking Hours: 8-10 hours per week Start Date: Immediately Duration: Approximately 9 monthsKey ResponsibilitiesPrescreening and Screening tasksReview charts from the site data baseMaintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and...

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...

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...

IQVIA Belgium is seeking a Clinical Research Associate to support monitoring visits, recruitment plans, and regulatory compliance across multiple therapeutic areas. You will work in a Belgium-based role with travel flexibility and contribute to delivering high-quality clinical research services.The position requires a university degree in a scientific...

Company DescriptionOur client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research AssociateJob OverviewMonitoring clinical studies in phases...

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical / Country Operations team in Belgium. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous...

LocationSAINT LOUIS, MO 63110 Scheduled Hours40 Position SummaryCoordinates clinical trials invoicing and payment reconciliation. Reviews clinical trial protocols and negotiated budgets to determine research charges and appropriate funds. Coordinates with numerous departments to establish study specific billing plans. Serves as a point of contact to...

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...

Clinical Research Associate For candidates able to start before December 2026, a discretionary sign‑on bonus of up to 4,300 EUR may be offered, with the final amount confirmed at offer stage, subject to role level and relevant experience.IQVIA Belgium is looking for talented and motivated team member to join our Sponsor dedicated team CRA (Junior -...

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...