Oncology Clinical Research Associate: Site Monitor

Job Description

Qualifications

• •Candidates must hold a Bachelor’s in Life Sciences and be eligible to work in the U.S. ICON offers competitive salaries and a variety of benefits aimed at well-being and work-life balance

Benefits

• •#J-18808-Ljbffr

Responsibilities

• •A leading clinical research organization in Connecticut is seeking a Clinical Research Associate with over two years of on-site monitoring experience, particularly in Oncology studies
• •The role involves ensuring compliance, conducting site visits, and collaborating with cross-functional teams