The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials
Job Summary
The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
Candidates must possess fluency in Dutch, English, and French to effectively communicate with investigative sites and clients across Belgium.
The position offers the opportunity to work fully remote or hybrid from Brussels, with travel requirements generally ranging between 60-80%.
Matching Summary
The role involves conducting remote or on-site visits to assess protocol and regulatory compliance while managing required documentation for clinical trials.
Skills & Requirements
Must-have
2+ years independent CRA experience
Fluency in Dutch, English, and French
Valid full driver's licence
Risk-based monitoring approach
ICH-GCP guidelines knowledge
On-site and remote monitoring skills
Nice-to-have
Critical thinking and problem-solving
Collaborative relationship building
Process improvement initiatives
Strong presentation skills
Flexible and adaptable mindset
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
Minimum 2 years of clinical research monitor experience