Clinical Research Associate II

• 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.

• 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.

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

Panda International