The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance
Job Summary
The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance.
Candidates must be prepared to travel 60-80% of the time to conduct site visits, verify data accuracy, and manage essential documents.
The position requires maintaining collaborative relationships with investigational sites while representing PPD in the global medical research community.
Matching Summary
The role involves performing and coordinating all aspects of clinical monitoring and site management to ensure protocol and regulatory compliance.
Skills & Requirements
Must-have
ICH GCP and FDA guidelines compliance
Source document verification (SDV)
60-80% travel requirement
Investigational product inventory management
Clinical Trial Management System usage
Nice-to-have
Effective interpersonal communication skills
Adaptability in diverse scenarios
Collaborative relationship building
Strong business writing standards
Team contribution and idea sharing
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
1 year of experience as a clinical research monitor
Valid driver's license where applicable
Completion of PPD Drug Development Fellowship or equivalent