MedTech Clinical Research Associate - Field Monitoring

Progressive

Brussel Hoofdstad

On-site

EUR 52,000 - 75,000

Full time

14 days+

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Progressive in Belgium is seeking a Clinical Research Associate to manage study activities across multiple sites for MedTech projects. You will ensure high-quality data collection, safeguard participant safety, and act as liaison between clinical teams and site personnel.

The role requires collaboration with investigators, vendors, and internal stakeholders, adherence to GCP and regulations, and travel up to 80% to monitor sites and support training.

Qualifications

  • Bachelor's degree with minimum two years of relevant experience, or a Master’s/PhD/MD/PharmD with at least one year of relevant experience.
  • Previous clinical research experience is required.
  • Experience in medical device monitoring or similar clinical monitoring activities is required.
  • Professional certifications such as CCRA, RAC, or CDE are an advantage.

Responsibilities

  • Monitor the safety and well-being of study participants at assigned sites.
  • Conduct monitoring visits to ensure protocol adherence and data accuracy.
  • Support the operational execution of clinical trials and data collection.
  • Review Investigator Site Files to ensure regulatory compliance.
  • Loster site performance, and coordinate with investigators and vendors.

Skills

Leadership
Communication
Presentation
Stakeholder mgmt
Project management
Multitasking
Microsoft Office

Education

Bachelor's degree
Master's degree or higher (preferred)

Tools

Microsoft Office

Job description

Progressive in Belgium is seeking a Clinical Research Associate to manage study activities across multiple sites for MedTech projects. You will ensure high-quality data collection, safeguard participant safety, and act as liaison between clinical teams and site personnel.

The role requires collaboration with investigators, vendors, and internal stakeholders, adherence to GCP and regulations, and travel up to 80% to monitor sites and support training.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

MedTech Clinical Research Associate | Travel‑Heavy
MedTech Clinical Research Associate | Travel‑Heavy

Pauwels Consulting • Machelen

On-site
EUR 42,000 - 66,000
Clinical Research Associate
Clinical Research Associate

Pauwels Consulting • Machelen

On-site
EUR 42,000 - 66,000
Clinical Research Associate – Site Monitoring & Growth
Clinical Research Associate – Site Monitoring & Growth

IQVIA LLC • Zaventem

On-site
EUR 50,000 - 65,000
Company car
Mobile phone
Benefits package
Rising Clinical Research Associate - Site Monitoring
Rising Clinical Research Associate - Site Monitoring

IQVIA • Brussel Hoofdstad

On-site
EUR 65,000 - 75,000
Company car
Mobile phone
Benefits package
Clinical Research Associate: Site Monitoring Leader
Clinical Research Associate: Site Monitoring Leader

Allucent • Scherpenheuvel-Zichem

On-site
EUR 55,000 - 75,000
Clinical Project Associate: Site Coordination & Compliance
Clinical Project Associate: Site Coordination & Compliance

Syneos Health, Inc. • Machelen

On-site
EUR 45,000 - 60,000
Remote CRA: Medical Device Clinical Trials & Monitoring
Remote CRA: Medical Device Clinical Trials & Monitoring

EPM Scientific • Brussel Hoofdstad

On-site
EUR 42,000 - 65,000
Senior Clinical Research Associate
Senior Clinical Research Associate

AL Solutions • Vlaanderen

Hybrid
EUR 65,000 - 85,000
Flexible hybrid work
Modern offices
Professional development
+1
Clinical Research Associate
Clinical Research Associate

Oxford Global Resources • Brussel

On-site
EUR 55,000 - 75,000
Clinical Project Associate
Clinical Project Associate

Syneos Health, Inc. • Machelen

On-site
EUR 45,000 - 60,000