Clinical Research Associate II (East Coast or Midwest)

📋 Description

• Perform on-site and remote monitoring across assigned sites and studies.
• Manage site relationships with autonomy; conduct SDV/SDR; resolve findings and protocol deviations.
• Maintain inspection-ready documentation and escalate risks with recommendations.
• Collaborate with site staff to ensure protocol adherence and study activity completion.
• Prepare monitoring visit reports and follow-up communications.
• Travel up to 60-70% as needed.

🎯 Requirements

• Bachelor's degree in life sciences or health-related field or equivalent experience.
• 3-5 years of clinical research monitoring experience with independent site management.
• Working knowledge of ICH-GCP E6(R2) and regulatory requirements.
• Ability to independently plan, conduct, and report on site visits (on-site and remote).
• Proficiency with EDC, CTMS, and eTMF systems.
• Strong written and verbal communication; ability to liaise with sites and cross-functional teams.

🎁 Benefits

• Travel: up to 60-70%
• Office/field-based role with remote work options