Join a leading MedTech organization as a Clinical Research Associate II, where you'll manage clinical activities across multiple study sites. Ensure patient safety, protocol compliance, and high-quality data collection while building strong relationships with site staff and stakeholders. Engage in patient recruitment, training initiatives, and support continuous improvement efforts. This role offers the opportunity to travel extensively and contribute to innovative clinical systems and processes. Delve deeper to learn about the benefits of joining our team.

Over het bedrijf

Panda International

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Job Role: Clinical Research Associate II – MedTech
About the Role:

A leading MedTech organization is seeking a detail-oriented and proactive Clinical Research Associate II (CRA II) to join the MedTech Clinical Operations team. In this role, you will manage clinical activities at multiple study sites, ensuring patient safety, protocol compliance, and high-quality data collection, while fostering strong relationships with site staff and internal stakeholders.

Key Responsibilities:

Manage clinical study activities across multiple sites for assigned projects.
Ensure study site compliance with protocols, SOPs, GCP, and regulatory requirements.
Conduct site visits, monitor performance, and provide timely support to resolve site issues.
Verify Investigator Site Files and support documentation maintenance.
Support patient recruitment, retention, and training initiatives.
Facilitate internal communication of key study data and events.
Participate in implementation of new clinical systems and processes.
Interface and collaborate with investigators, IRBs/ECs, vendors, and internal stakeholders.
Maintain accurate study site status knowledge and provide updates to project teams.
Support internal continuous improvement and operational excellence initiatives.

Requirements:

Bachelor’s degree in Life Science, Physical Science, Nursing, or Biological Science (Master’s/PhD/MD/PharmD preferred).
Minimum 2 years of relevant clinical research experience; 1 year with advanced degree.
Previous medical device monitoring experience or equivalent.
Knowledge of regulations and standards in clinical research for medical devices/combination products.
Relevant industry certifications preferred (e.g., CCRA, RAC, CDE).
Strong written and verbal communication, leadership, and organizational skills.
Proficiency in Microsoft Office (Excel, Word, PowerPoint).
Clinical/medical background is a plus.
Ability to travel up to 80% of the time.

Practical’s:

Location: Diegem, Belgium
Duration: 12-month contract
Start Date: ASAP
Work Model: Full-time, travel required up to 80%

Interested or know someone who might be?
Send your CV or inquiries to via de button "Solliciteer nu" op deze pagina. to apply or learn more.

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