Clinical Research Associate II

Role Overview

• Monitors investigator sites with a risk-based monitoring approach
• Conducts monitoring tasks in accordance with the approved monitoring plan
• Participates in the investigator payment process
• Ensures audit readiness and develops collaborative relationships with investigational sites
• Keeps in contact with investigative sites to confirm that the protocol is being followed

Requirements

• Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 year as a clinical research monitor) or completion of PPD Drug Development Fellowship
• Valid driver's license where applicable.

Benefits

• Health insurance
• Paid time off
• Remote work options