Clinical Research Associate (CRA) II

Role Overview

Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation. Represents PPD in the global medical research community and develops and maintains collaborative relationships with investigational sites.

What You Will Do

Monitors investigator sites, conducts site visits, documents observations, escalates deficiencies, maintains regular contact with investigative sites, and performs trial close out and retrieval of trial materials.

Why It Might Be a Fit

Requires a Bachelor's degree in a life sciences related field or equivalent, 1 year of experience as a clinical research monitor, and good communication, organizational, and interpersonal skills.

Requirements

• Bachelor's degree in a life sciences related field or equivalent
• 1 year of experience as a clinical research monitor
• Valid driver's license where applicable