Senior Clinical Research Associate Oncology ICON
Overview
Lead clinical trial monitoring oversight and team development as a Sr. CRA at ICON. Oversee multi-site oncology trials ensuring regulatory compliance and data integrity. Drive operational excellence while fostering collaborative environments. Seeking a leader with 5+ years experience to elevate trial execution and mentor junior staff.
What You'll Do5
- 1Lead site management activities including selection initiation monitoring and close-out to guarantee protocol adherence
- 2Serve as primary technical liaison for clinical sites resolving complex queries and maintaining engagement
- 3Conduct rigorous source data verification and monitor protocol deviations to preserve data quality
- 4Mentor CRAs provide professional development guidance and uphold best practices across studies
- 5Partner with cross-functional teams to execute trials successfully
Requirements7
- 15+ years building ETL pipelines with Spark and Airflow
- 2Bachelor's degree in healthcare science or related discipline
- 3Extensive experience as Clinical Research Associate in pharma or CRO sector
- 4In-depth knowledge of ICH-GCP guidelines and regulatory frameworks
- 5Strong leadership abilities with proven track record of motivating teams
- 6Excellent communication and problem-solving skills with proactive approach
- 7Willingness to travel approximately 60% of time
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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