Clinical Research Associate
$91.34k - $114.17kICON
ICON is seeking a Clinical Research Associate II with oncology/hematology experience to conduct clinical trial monitoring activities, ensure protocol compliance, and maintain data integrity across sponsor-dedicated studies in the northeastern United States.
Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolve queries to maintain high-quality clinical data
- Contribute to preparation and review of study documentation including protocols and reports
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 1 year of clinical research associate experience
- Monitoring experience with hematology/oncology studies
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to work independently and collaboratively in fast-paced environment
- Willingness to travel approximately 60%; must be located in specified northeastern states
Compensation: $91,336–$114,170 base
Vacancy posted 10 days ago
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