Responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, SOPs, GCP, and applicable regulations from study start-up through to site closure
Job Summary
Responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, SOPs, GCP, and applicable regulations from study start-up through to site closure.
Co-create site-level recruitment and retention strategies and implementation of mitigation actions in partnership with other functional areas.
We offer a competitive salary and extensive benefits package, a flexible working environment, and career development opportunities.
Matching Summary
Responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, SOPs, GCP, and applicable regulations from study start-up through to site closure.
Skills & Requirements
Must-have
GCP, local laws, and regulations knowledge
Site monitoring and oversight
Data accuracy and query resolution
Protocol compliance and inspection readiness
Nice-to-have
Strong communicator and problem solver
Team player and quick learner
Coaching and mentoring skills
Key Requirements
Minimum of 3 years of clinical trial monitoring experience
BA/BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience)