11 beste vacatures voor de functie van regulatory affairs specialist in vlaams gewest (nieuwe medewerkers gezocht)

Clinical research & implementation specialist
FibriCheck —Hasselt België
- Onderzoek
- Master
- Projectmanagement
Regulatory Affairs Specialist
Hologic —Zaventem
- € 40.000 - € 50.000 per jaar
- Microsoft Powerpoint
- Microsoft Word
- Spaans
Product Safety & Regulatory Compliance Specialist EU (M/V/X)
Lawter —Kallo
- Master
- Bachelor
- JavaScript
Regulatory Affairs Specialist
Nipro —Mechelen
- Analytisch vermogen
- Bachelor
Regulatory Affairs Specialist
Nipro Europe Group Companies —Mechelen
- Analytisch vermogen
- Bachelor
Senior Regulatory Affairs Specialist (Biocides)
Elements Advisory —Gent
- Doctoraat
- Master
- Projectmanagement
Quality Specialist
Hologic —Zaventem
- € 50.000 - € 70.000 per jaar
- ERP systemen
- Microsoft Office
- Bachelor
Regulatory Affairs - Environment
Nipro —Mechelen
- Hybride werken
- Master
- Bachelor
- ICT
Regulatory Affairs - Environment
Nipro Europe Group Companies —Mechelen
- Master
- Bachelor
- ICT
Quality Specialist (Distribution Center)
Abbott Laboratories —Machelen
- Voltijds
- Engels
- Microsoft Office
- Bachelor
7 dagen
Principal Corporate Counsel
Cisco Systems —Diegem
- Voltijds
- Artificiële intelligentie
- Tijdsbeheer

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Regulatory Affairs Specialist
Hologic —Zaventem
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Regulatory Affairs - Environment
Nipro —Mechelen
Collaborate within NEGC ESG team. (Pro-)Active Participation as RAQACA team member (20%). This entails Regulatory Intelligence for the EMEA market in the…

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Clinical research & implementation specialist

FibriCheck
Hasselt België

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Vacaturegegevens

Extralegale voordelen

Een gsm voor professioneel gebruik

Kwalificaties

Frans
Onderzoek
Master
Projectmanagement
Bachelor
Cardiologie
SaaS
Communicatieve vaardigheden
Duits
Nederlands

Volledige vacaturetekst

Help us change the way the world detects and manages cardiovascular disease

FibriCheck is a fast-growing medtech scale-up on a mission to prevent strokes and improve cardiac care worldwide. Our certified AI-powered Software as a Medical Device (SaMD) solution allows people to detect and monitor cardiovascular diseases anytime and anywhere on everyday devices like a smartphone.

We empower patients and consumers with actionable health insights, support healthcare providers with better data, and help healthcare systems deliver more proactive, cost-efficient care. With partnerships across hospitals, insurers, wearable manufacturers and telehealth platforms, FibriCheck is transforming how heart health is managed: digitally, remotely, and at scale.

Headquartered in Belgium and expanding rapidly with a strong focus on the US, we are now looking for a proactive Clinical Research & Implementation Specialist to be the vital link between our technology and clinical practice.

Your role

You are the “boots on the ground” clinical and research expert. Your focus is threefold: (1) ensuring successful medical implementations, (2) coordinating internal and external clinical studies, and (3) maintaining and improving clinical regulatory documentation. You will translate commercial agreements into measurable clinical impact, ensuring our partners (hospitals, researchers, wearable providers, etc.) achieve their goals while maintaining scientific rigor.

Key responsibilities

Drive clinical implementation & partner success

Manage the end-to-end setup for hospitals and clinical partners, ensuring smooth workflow integration and high adoption.
Leverage your scientific and communication skills to train healthcare professionals, optimize their clinical pathways, and troubleshoot operational issues.
Translate operational field insights into actionable input for product, commercial, and medical affairs to shape market strategy and product improvements.
Monitor usage and performance metrics to proactively intervene and ensure long-term value for the partner.

Coordinate clinical research

Oversee and manage the setup and execution of clinical studies, ensuring feasibility, proper investigator training, efficient workflows, and troubleshoot operational issues.
Support internal and external research initiatives, ensuring compliance with local requirements.
Translate research insights into actionable input for product, commercial, and medical affairs to shape market strategy and product improvements.

Clinical and regulatory excellence

Actively maintain and improve clinical regulatory documentation ensuring all activities remain compliant, including but not limited to clinical evaluation, literature search, post-market surveillance, and regulatory submissions
Translate regulatory field insights into actionable input for product, commercial, and medical affairs to shape market strategy and product improvements.

What you bring

3-5+ years in a customer-facing role (e.g., clinical application specialist, research coordinator, implementation manager) within MedTech, SaaS, or Digital Health. Prior experience in cardiology is a plus.
Bachelor’s or Master’s degree in life sciences, biomedical sciences, nursing, or related field.
You are analytical, organized, and bring strong project management skills, enabling you to manage timelines and coordinate multiple projects & stakeholders.
You are a clear and effective communicator who can quantify value and articulate complex scientific concepts in a structured and accessible way.
Familiarity with clinical evaluations and research methodologies is highly valued.
Fluent in Dutch and English. Proficiency in German or French is a strong asset.
Willingness to travel internationally (EU & US) up to ~30%.

What we offer

A direct and customer-facing role in a mission-driven company reducing the burden of cardiovascular disease.
A dynamic environment where you can develop expertise in US/EU market access and clinical innovation.
Hybrid working model with autonomy and a competitive package.

Energized by our mission and can’t wait to use your first-class talent? Send your resume and a brief motivation to [email protected]. If you are energized by our mission but don’t check every single box, we still encourage you to apply.

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Verfijn je zoekopdracht

regulatory affairs specialist vacatures in vlaams gewest

Clinical research & implementation specialist

Regulatory Affairs Specialist

Product Safety & Regulatory Compliance Specialist EU (M/V/X)

Regulatory Affairs Specialist

Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist (Biocides)

Quality Specialist

Regulatory Affairs - Environment

Regulatory Affairs - Environment

Quality Specialist (Distribution Center)

Principal Corporate Counsel

Other jobs to consider

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs specialist in vlaams gewest

Zoek vacatures in meer locaties

Help us change the way the world detects and manages cardiovascular disease

Your role

Key responsibilities

Drive clinical implementation & partner success

Coordinate clinical research

Clinical and regulatory excellence

What you bring

What we offer

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