Serve as a primary contact point between the sponsor and the investigational site for the conduct of complex early development and/or clinical pharmacology studies
Job Summary
Serve as a primary contact point between the sponsor and the investigational site for the conduct of complex early development and/or clinical pharmacology studies.
Ensure inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), Healthcare compliance (HCC) requirements, applicable regulations, and guidelines.
We offer a competitive salary and extensive benefits package, a flexible working environment, and career development opportunities.
Matching Summary
Serve as a primary contact point between the sponsor and the investigational site for the conduct of complex early development and/or clinical pharmacology studies.
Skills & Requirements
Must-have
Clinical trial monitoring experience
ICH-GCP knowledge
Company SOPs
Local laws and regulations
Risk-based monitoring approaches
Trial management systems
Nice-to-have
Process improvement
Training and mentoring
Flexible mindset
Fast-paced environment
Work-life balance
Key Requirements
Minimum 3 years clinical trial monitoring experience
BA or BS degree in Life Sciences or equivalent experience