Clinical Research Coordinator II
Lowell, Massachusetts, United States of America
Full Time
2 hours ago
$47,924 - $59,894 USD
No Visa Sponsorship
About this role
Role Overview
- Supports clinical trials by recruiting and screening participants.
- Conducts informed consent and coordinates protocol‑required visits, procedures, and follow‑up.
- Ensures accurate data collection and quality review of Case Report Forms.
- Maintains regulatory documentation and assists with IRB submissions.
- Arranges and performs study‑related tests within training scope.
- Monitors adverse events and manages study supplies.
- Supports sponsor site visits and ensures protocol compliance.
Requirements
- Bachelor’s degree OR High School Diploma or equivalent AND Four (4) years of related experience.
- Basic Life Support (BLS) certification may be required based on specific role requirements.
- Two (2) years in research related activities.
- Five (5) years in research related activities (preferred).
- Previous experience in clinical trials (preferred).
- IATA Hazardous Good Shipping certification (preferred).
- CITI Human Research Protection certification (preferred).
Benefits
- Health insurance
- Retirement plans
- Flexible work arrangements
- Professional development opportunities
- Paid time off