clinical research manager

FUNCTIEOMSCHRIJVING In de rol van Clinical Trial & Real World Evidence Manager ben je verantwoordelijk voor het ontwerpen, uitvoeren en strategisch integreren van klinische studies, observationeel onderzoek en consumentenonderzoek, in lijn met de wereldwijde strategie van Metagenics. Wat moet je precies doen? Onderzoeksstrategie & Studieontwerp: -...

DescriptionQualifications, skills, and all relevant experience needed for this role can be found in the full description below.In de rol van Clinical Trial & Real World Evidence Manager ben je verantwoordelijk voor het ontwerpen, uitvoeren en strategisch integreren van klinische studies, observationeel onderzoek en consumentenonderzoek, in lijn met de...

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...

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...

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...

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...

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,...

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,...

Bij Select Projects draait alles om jou als consultant. We willen dat jij elke dag met goesting aan de slag gaat, jezelf kan zijn en de ruimte krijgt om te groeien. Als consultant werk je aan uitdagende projecten waar je jouw talent volop kan inzetten en verder ontwikkelen. Je krijgt vertrouwen, autonomie en de kans om bij te leren via opleidingen, coaching...

Select Projects in België zoekt een Clinical Research Manager die internationale klinische studies coördineert van studieopstart tot afsluiting, samen met onderzoekers, CRA’s en externe partners. Je bewaakt tijdlijnen en budgetten en zorgt voor kwaliteit en compliance.Je werkt aan protocollen, documentatie en safety reporting; je leidt een team van...

Take the next step in your clinical research career and contribute to high quality clinical studies within the medical device sector. We are looking for 2 profiles: • a Clinical Research Associate who combines strong site management skills with a solid understanding of clinical research regulations. • a Senior Clinical Research Associate to take...

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...

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...

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...

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...

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...

For our client, a global medical device company, we are looking for a Clinical Research Associate. Position Summary The 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...