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 comp ...
jobdetails
overzicht
- zaventem, vlaams-brabant
- voltijds
gepubliceerd op 31 juli 2026
- referentienummer
- JN -072026-618673
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P
peggy vancoillie
Recruitment Consultant
volgende stappen
randstad professional
je bent een krak in finance, life sciences, hr, sales & marketing, engineering, healthcare of office & administration support. en je wil uitblinken in een van deze domeinen? da's helemaal oké. jij kiest hoe je je loopbaan invult.
jobdetails
Senior Clinical Research Specialist – MedTech (Electrophysiology)
letion within a collaborative team, we want to hear from you!Job Summary
toon meerAs a Senior Clinical Research Specialist, you will support one or several clinical trials within the Clinical R&D Department, playing a vital role in ensuring compliance with timelines, regulatory standards, and study milestones. You will oversee the end-to-end execution of clinical studies—spanning both pre-market and post-market phases in the cardiology and electrophysiology space. Working in a hybrid setup based in Diegem, you will collaborate closely with trial sites, vendors, CRAs, and cross-functional teams across the EMEA region.
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.
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, you will support one or several clinical trials within the Clinical R&D Department, playing a vital role in ensuring compliance with timelines, regulatory standards, and study milestones. You will oversee the end-to-end execution of clinical studies—spanning both pre-market and post-market phases in the cardiology and electrophysiology space. Working in a hybrid setup based in Diegem, you will collaborate closely with trial sites, vendors, CRAs, and cross-functional teams across the EMEA region.
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.
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belangrijkste verantwoordelijkheden
- Study Execution & Management: Oversee and execute feasibility, site selection, set-up, conduct, and closure of clinical trials across allocated countries in accordance with ICH-GCP, local legislation, and SOPs.
- Site & Vendor Collaboration: Serve as the primary contact for clinical trial sites, interface with site personnel, IRBs/ECs, vendors, and oversee Clinical Research Associates (CRAs).
- Document & Trial Material Management: Contribute to the development of trial documentation (protocols, informed consents, CRFs, monitoring plans, study manuals) and oversee the ordering, tracking, and accountability of investigational devices.
- Data Review & Safety Coordination: Conduct clinical data reviews to prepare for statistical analyses. When acting as Clinical Safety Coordinator, coordinate all trial safety activities, safety management plans (SMP), adverse event reporting, and safety board meetings.
- Monitoring & On-Site Support: Perform monitoring activities (site qualification, initiation, interim monitoring, or close-out visits) as needed.
- PMCF & Strategy: Assist with Post-Market Clinical Follow-up (PMCF) plans and evaluation reports, and contribute to global Evidence Generation/Dissemination Strategies (EGS/EDS).
- Leadership & Budgeting: Mentor team members, support study budget activities, and ensure deliverables are met on time and within budget.
vaardigheden
Fasen van Klinisch OnderzoekMedical Device DirectiveClinical TrialsClinical Trial Protocolkwalificatie
Education & Experience- Education: Minimum of a Bachelor’s degree in Life Science, Physical Science, Biological Science, or Nursing.
- Experience:
- Bachelor’s with 4+ years, Master’s with 3+ years, or PhD with 2+ years of relevant clinical research experience.
- Proven experience in managing all aspects of clinical research, including pre- and post-market studies.
- Background in Pharmaceuticals or Medical Devices (MedTech) is required/highly preferred.
- Specific experience in cardiology or electrophysiology is a strong advantage.
- Strong understanding of clinical research science, global trial regulations, and GCP principles.
- Industry certifications (e.g., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR) are preferred.
- Solid project management skills with a track record of delivering clinical projects on time and within budget.
- Technical writing and data review skills.
- Languages: Fluent in English (written and spoken); knowledge of additional European languages is an asset.
- Mindset: Proactive, assertive, highly adaptable, strong communicator, and collaborative team player.
- Mobility & Work Model: Based in Belgium. Hybrid model (typically 3 days onsite in Diegem / 2 days remote, adjusted per study phase). Willingness to travel up to 20% (primarily within EMEA for site qualification and clinical trial support).
voordelen
What We OfferOur 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
- 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
