research clinical

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.General Description:Acts as line manager for trial...

For our client, a global medical device company, we are looking for a Clinical Research Associate.Position SummaryThe Clinical Research Associate (CRA) is responsible for monitoring and overseeing clinical investigations involving medical devices to ensure compliance with applicable regulations, Good Clinical Practice (GCP), study protocols, and company...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.General DescriptionActs as line manager for trial...

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...

Clinical monitoringAt 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...

We are looking for a motivated Clinical Research Associate (CRA) to support the successful execution of clinical studies within an innovative MedTech environment. In this role, you will be responsible for monitoring clinical trial activities across multiple study sites, ensuring compliance with study protocols, regulatory requirements, and Good Clinical...

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...

Onze klant, gevestigd in Oostende, is een producent van hoogwaardige micronutritie.Ze produceren perfecte en evenwichtige gedoseerde voedingssupplementen van de meest kwalitatieve grondstoffen zodat ze snel en veilig door ons lichaam worden opgenomen.JobomschrijvingWat moet je precies doen?Onderzoeksstrategie & StudieontwerpOntwerpen en afstemmen van...

Onze klant, gevestigd in Oostende, is een producent van hoogwaardige micronutritie.Ze produceren perfecte en evenwichtige gedoseerde voedingssupplementen van de meest kwalitatieve grondstoffen zodat ze snel en veilig door ons lichaam worden opgenomen.FunctieomschrijvingIn de rol van Clinical Trial & Real World Evidence Managerben je verantwoordelijk voor het...

Our client, a leading MedTech organization, is seeking a Clinical Research Associate to manage clinical activities across various study sites. The role focuses on overseeing site performance, conducting monitoring visits, and ensuring the delivery of high-quality data for clinical projects.Manage clinical study site activities and oversee performance for...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior Clinical...

📍 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...

We are the people who give possibilities purposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

Snr CRA - Clinical Site ManagementICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

What You'll Do: 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...

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,...

Snr CRA - Clinical Site 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...

Jobat zoekt een ervaren onderzoeksspecialist in Oostende voor het ontwerp en de uitvoering van cross-functionele studies in de voedingssupplementensector. U ontwikkelt onderzoeksstrategieën, coördineert data-verzameling en werkt samen met klinische onderzoekers en marketing om wetenschappelijke bevindingen te vertalen naar claims en marktpositionering.De...

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...

What You'll Do: 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...