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  1. home
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  5. clinical research associate
  6. clinical research specialist
clinical research associate
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clinical research specialist

zaventem, vlaams-brabant
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jobdetails

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  • zaventem, vlaams-brabant
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  • voltijds

gepubliceerd op 31 juli 2026

referentienummer
JN -072026-618655
contacteer ons.

neem contact met ons op voor al je vragen.

P

peggy vancoillie

Recruitment Consultant

lifesciences.vlaanderen@randstad.be

volgende stappen

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  • maak een job alert aan
  • maak een account aan
  • vacatures zoeken

randstad professional

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jobdetails

Are you passionate about advancing healthcare technologies and driving breakthrough clinical studies? Join a global leader in medical technology as a Clinical Research Specialist focusing on innovative Electrophysiology solutions. In this high-impact role, you will bridge the gap between cutting-edge clinical R&D and hands-on medical applications in hospitals across the EMEA region. If you thrive in a dynamic, collaborative environment where your work directly touches patient lives, we want to hear from you!


...

Job Content

As a Clinical Research Specialist, you will support the end-to-end execution of company-sponsored clinical trials within our client's MedTech Electrophysiology division. Working under general guidance within the Clinical R&D department, you will build strong collaborative relationships with trial sites, physicians, ethics committees, and cross-functional internal teams.

From guiding hospital teams in the lab and managing ethical and regulatory submissions to handling clinical safety coordination and data reviews, you will serve as a trusted, knowledgeable cornerstone for allocated clinical studies.


Should you have any questions about this position, please feel free to get in touch with Peggy Vancoillie. She can be reached at +32 2 472 92 14 or peggy.vancoillie@randstad.be. We look forward to hearing from you.





toon meer

Are you passionate about advancing healthcare technologies and driving breakthrough clinical studies? Join a global leader in medical technology as a Clinical Research Specialist focusing on innovative Electrophysiology solutions. In this high-impact role, you will bridge the gap between cutting-edge clinical R&D and hands-on medical applications in hospitals across the EMEA region. If you thrive in a dynamic, collaborative environment where your work directly touches patient lives, we want to hear from you!


Job Content

As a Clinical Research Specialist, you will support the end-to-end execution of company-sponsored clinical trials within our client's MedTech Electrophysiology division. Working under general guidance within the Clinical R&D department, you will build strong collaborative relationships with trial sites, physicians, ethics committees, and cross-functional internal teams.

From guiding hospital teams in the lab and managing ethical and regulatory submissions to handling clinical safety coordination and data reviews, you will serve as a trusted, knowledgeable cornerstone for allocated clinical studies.

...

Should you have any questions about this position, please feel free to get in touch with Peggy Vancoillie. She can be reached at +32 2 472 92 14 or peggy.vancoillie@randstad.be. We look forward to hearing from you.





toon meer
  • belangrijkste verantwoordelijkheden

    • Study Execution & Site Management: Support trial feasibility, site selection, initiation, conduct, and close-out in compliance with ICH-GCP, local legislation, and company SOPs. Act as the primary contact for clinical trial sites and Clinical Research Associates (CRAs).
    • On-Site & Lab Support: Work directly in hospital settings and labs alongside physicians to ensure procedural protocol compliance, data collection, and site qualification.
    • Documentation & Submissions: Assist in developing study protocols, informed consent forms, CRFs, monitoring plans, and annual reports. Handle regulatory and ethical submissions.
    • Safety & Regulatory Coordination: Coordinate study safety activities, safety management plans (SMP), adverse event reporting, and safety board meetings across cross-functional teams.
    • Device & Trial Material Tracking: Oversee the ordering, tracking, accountability, and inventory of investigational devices and trial materials.
    • Project & Data Management: Track assigned project budgets, oversee investigator agreements and payments, and assist in clinical data reviews to prepare data for statistical analyses and publications.


  • vaardigheden

    Fasen van Klinisch Onderzoek
    Medical Device Directive
    Clinical Trials
    Clinical Trial Protocol
  • kwalificatie

    Education & Experience
    • Education: Minimum of a Bachelor’s degree preferably in Life Science, Physical Science, Nursing, or Biological Science (Master’s or PhD is a plus).
    • Experience: Minimum of 2 years (BS) or 1 year (MS/PhD) of relevant clinical research experience, preferably within medical devices.
    • Location: Must be based in Belgium, with the willingness and flexibility to travel across the EMEA region (~20% travel).
    Skills & Competencies
    • Technical Knowledge: Strong understanding of clinical research processes, global trial regulations, and standard operating procedures (ICH-GCP, ISO 14155, MDR).
    • Software Proficiency: High proficiency in Microsoft tools, particularly Excel.
    • Mindset & Style: Assertive, independent worker who communicates proactively and thrives under minimal supervision for routine tasks.
    • Languages: Fluent in English (written and spoken). Proficiency in any additional European language is an advantage.
    • Certifications: Relevant industry certifications (e.g., GCP, CCRA, CCRC, CCRP, RAC) are preferred.


  • voordelen

    Our Offer (Employed Consultant)
    • Competitive gross salary with 13th month and double holiday pay
    • Monthly net allowance
    • Meal vouchers & eco vouchers
    • Choice between company car with fuel/charging card (SalSa plan) or mileage reimbursement for using your own car
    • Hospitalization insurance from day 1 + optional outpatient insurance (incl. dental care)
    • Group insurance (pension savings)
    • Cafeteria plan (Flex Income Plan)
    • 4 weeks of statutory holiday + 12 ADV days + seniority leave
    • Possibility to work from home (depending on project)
    • Benefits at Work discount platform
    • Referral bonus when you recommend a new colleague
    • Personal follow-up via account manager, HR/L&D support, access to training, learning tools, and certifications
    • Networking events and internal activities to stay connected with colleagues and the organization
    Prefer to work as a Freelance Consultant?
    • We pay your invoices on time and correctly (30 days)
    • Our team of recruiters and account managers is closely involved in your career and follows you up
    • Towards the end of your project, we proactively look for your next assignment


contacteer ons.

neem contact met ons op voor al je vragen.

P

peggy vancoillie

Recruitment Consultant

lifesciences.vlaanderen@randstad.be

gerelateerde jobs.

alle clinical research associate vacatures in zaventem
  • clinical research specialist

    • zaventem, vlaams-brabant
    • vast
    Senior Clinical Research Specialist – MedTech (Electrophysiology)Are you an experienced clinical research professional looking to make a direct impact on groundbreaking medical technologies? Do you thrive in a dynamic, global environment where innovation meets patient care? If you are ready to drive complex clinical trials from set-up to completion within a collaborative team, we want to hear from you!Job SummaryAs a Senior Clinical Research Specialist,
    31 juli 2026
    Senior Clinical Research Specialist – MedTech (Electrophysiology)Are you an experienced clinical research professional looking to make a direct impact on groundbreaking medical technologies? Do you thrive in a dynamic, global environment where innovation meets patient care? If you are ready to drive complex clinical trials from set-up to completion within a collaborative team, we want to hear from you!Job SummaryAs a Senior Clinical Research Specialist,
    toon jobdetails

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