A company is looking for a Lead Clinical Research Associate.
Key Responsibilities
Lead site management activities, ensuring compliance with study protocols and regulatory guidelines
Act as the primary contact for clinical sites, addressing queries and resolving issues to maintain site performance
Ensure data integrity through source data verification and monitoring for protocol deviations
Required Qualifications
Bachelor's degree in life sciences, nursing, pharmacy, or a related field; advanced degree preferred
Extensive experience as a Clinical Research Associate in the pharmaceutical, biotech, or CRO industry
In-depth knowledge of ICH-GCP guidelines and clinical trial processes
Strong leadership and mentoring skills
Proven ability to manage and motivate CRAs and site staff effectively
Clinical Research Associate • Lake Worth, Florida, United States