International conference on harmonization (ich) guidelines
Site monitoring visit execution
IQVIA UK is seeking a Clinical Research Associate to perform monitoring and site management tasks, ensuring compliance with study protocols and regulatory requirements. The ideal candidate will have a background in a scientific discipline and possess strong organizational and communication skills
Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
Candidates must evaluate the quality of study site practices and ensure adherence to applicable regulations while managing data integrity.
IQVIA is a leading global provider offering competitive compensation ranging from $47,400.00 to $169,300.00 annually.
Matching Summary
Match Score: 75
IQVIA UK is seeking a Clinical Research Associate to perform monitoring and site management tasks, ensuring compliance with study protocols and regulatory requirements. The ideal candidate will have a background in a scientific discipline and possess strong organizational and communication skills.
Salary
Base: $47,400.00 - $169,300.00; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare benefits included
Skills & Requirements
Must-have
Good Clinical Practice (GCP) knowledge
International Conference on Harmonization (ICH) guidelines
Site monitoring visit execution
Trial Master File maintenance
Subject recruitment plan management
Nice-to-have
Strong organizational and problem-solving skills
Effective time and financial management
Proficiency in Microsoft Office suite
Ability to establish client relationships
Key Requirements
Bachelor's Degree in scientific discipline or health care
Prior monitoring experience or CRA training program completion
Basic knowledge of clinical research regulatory requirements