clinical trial administrator
Enregistrez cette offre et organisez votre recherche
Créez un compte gratuit pour enregistrer des offres d'emploi, créer des alertes et revenir à cette liste depuis votre tableau de bord.
En continuant, vous acceptez nos Conditions d’utilisation & Politique de confidentialité.
- Clinical Study Site Management: 95%
- Administratieve
taken:
5%
-
key responsibilities
- Site Management & Monitoring: Je voert locatiebezoeken uit, ziet toe op de naleving van het studieprotocol en controleert of Investigator Site Files voldoen aan alle regelgeving.
- Kwaliteit & Veiligheid: Je waarborgt de veiligheid en het welzijn van proefpersonen, zorgt voor een nauwkeurige gegevensverzameling en voert werkzaamheden uit volgens SOP’s, GCP en wettelijke vereisten.
- Probleemoplossing: Je helpt locaties bij het snel oplossen van knelpunten en ondersteunt bij het opstellen van correctieve en preventieve acties (CAPA).
- Werving & Ondersteuning: Je ondersteunt patiëntenwerving en -behoud, helpt bij het organiseren van trainingen en onderhoudt contacten met onderzoekers, ethische commissies (IRB/EC) en leveranciers.
- Administratie & Naleving: Je blijft volledig op de hoogte van de websidestatus, volgt de Health Care Compliance-richtlijnen en ondersteunt bij de implementatie van nieuwe klinische systemen.
- qualifications
-
Opleiding:
Bachelor in een relevante richting (Life Sciences, Verpleegkunde, Biologie, Physical Science). Een Master, PhD, MD of PharmD is een pluspunt.
-
Ervaring:
Minimaal 2 jaar relevante ervaring met een bachelordiploma, of minimaal 1 jaar ervaring met een master of doctoraat.
- Specifieke
ervaring:
Aantoonbare ervaring in klinisch onderzoek en het monitoren van medische hulpmiddelen (medical devices) is vereist.
- Kennis: Grondige kennis van de regelgeving en standaarden binnen klinisch onderzoek en medische apparatuur. Goede beheersing van MS Office (Excel, Word, PowerPoint).
-
Vaardigheden:
Sterke communicatieve en organisatorische vaardigheden, leiderschapskwaliteiten en het vermogen om meerdere taken tegelijk te beheren binnen strakke deadlines.
- Troeven: Een klinische/medische achtergrond of relevante certificeringen (zoals CCRA, RAC, CDE) zijn een duidelijke meerwaarde. share this job.
-
Senior Business Analyst
Il y a 8 heures
Zaventem, Flanders, Belgique Next-Link Temps pleinOur client is transforming its fragmented legacy clinical data landscape into a modern, governed Clinical Data Layer (CDL). The objective is to centralize, manage, govern, and secure clinical data in compliance with regulatory and GxP requirements.The contingent will support the Clinical Data Layer initiative within the Ruby Program and act as the key...
-
Sorter medical samples | Inbound | 6-month assignment | ENG
Il y a 3 heures
Zaventem, Flanders, Belgique Adecco Temps pleinWe are looking for a sorter of medical samples for a company active in the pharmaceutical sector. The company is located in Zaventem. As a sample management associate you are responsible for organizing, tracking, and distributing samples used in research, testing, or clinical trials.Your tasks:-You perform simple inventory tracking procedures.-You receive...
-
Remote Dutch-Speaking Clinical Trial Psych Rater
Il y a 3 jours
Zaventem, Vlaams-Brabant, Belgique IQVIA Argentina Temps plein 2 500 € - 6 200 € ContratIQVIA, a global leader in clinical research services, is seeking a Clinical Trial Psych Rater (Dutch Speaking) for remote work in Belgium. The Part-time role involves reviewing rating scales, guiding rater methodology, and supporting performance through mock interviews, with approx.10–16 hours per month. Requirements include a Master’s degree in a...
-
Clinical Research Associate
Il y a 4 jours
Zaventem, Vlaams-Brabant, Belgique IQVIA Temps plein 42 000 € - 65 000 € ContratIQVIA Belgium is seeking a Clinical Research Associate to join our Sponsor dedicated team (Junior - Senior). You will conduct site visits, support recruitment planning, and ensure regulatory compliance while coordinating with study sites and client teams to advance clinical trials.The role requires a scientific degree, pharma/clinical trials experience, and...
-
Remote Clinical Study Manager – Oncology Trials Lead
Il y a 4 jours
Zaventem, Vlaams-Brabant, Belgique IQVIA Télétravail Temps plein 70 000 € - 110 000 € ContratIQVIA is seeking a Local Clinical Study Manager to lead trials across therapeutic areas in a home-based setting. The role supports multi-country delivery from Belgium, Denmark, Netherlands or Sweden, coordinating cross-functional teams and external vendors to ensure on-time, high-quality study execution.You will oversee monitoring activities, regulatory...
-
Senior Clinical Trial Manager
Il y a 6 jours
Zaventem, Vlaanderen, Belgique ICON Temps pleinSenior Clinical Trial 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...
-
Clinical Research Manager
Il y a 23 heures
Zaventem, Vlaanderen, Belgique BeiGene Temps pleinBeOne 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...
-
Clinical Operations Development Lead
Il y a 7 heures
Zaventem, Vlaanderen, Belgique Argenx Temps pleinFor the expansion of our Global Clinical Trial Operations team, argenx is looking for a Clinical Operations Development Lead.Key Accountabilities/Responsibilities:The Clinical Operations Development Lead (CODL) is responsible for the oversight of the clinical related activities within a specific therapeutic indication for an asset (CODL) or across all...
-
Senior Clinical Research Associate
Il y a 17 heures
Zaventem, Vlaanderen, Belgique ICON Temps pleinSnr 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...
-
Local Clinical Study Manager
Il y a 4 jours
Zaventem, Belgique IQVIA Temps pleinThe IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.We currently offer the...