International conference on harmonization ich guidelines
IQVIA is seeking a CRA 2 to perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements
Job Summary
IQVIA is seeking a CRA 2 to perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
The role involves evaluating study site practices, managing regulatory submissions, and ensuring data integrity through case report form completion and query resolution.
Candidates will collaborate with the study team to support project execution, manage site financials, and maintain compliant Investigator's Site Files.
Matching Summary
IQVIA is seeking a CRA 2 to perform site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
Salary
Base: $87,200.00 - $145,300.00 annualized; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare benefits included
Skills & Requirements
Must-have
1.5 years on-site oncology monitoring experience
Good Clinical Practice GCP compliance
International Conference on Harmonization ICH guidelines
Nice-to-have
Strong subject recruitment planning skills
Effective site communication and collaboration
Experience with Trial Master File maintenance
Key Requirements
Bachelor's Degree in scientific discipline or health care preferred
1.5 to 2 years of relevant CRA experience
Minimum 1.5 years of on-site oncology monitoring experience