What you will do

• Perform site monitoring and site management responsibilities through all phases of clinical study (e.g. site selection, site initiation, interim monitoring, and closeout)

• Conduct site visits for all phases (site qualification, site initiation, interim monitoring, and closeout)

• Ensure site compliance to clinical study protocol, applicable regulations and guidelines

• Ensure data integrity by verifying data in case report forms against source documents

• Identify and support site in addressing any noncompliance issues. 

• Collect and track regulatory documents, maintain trial master file (TMF) documentation and ensure accuracy

• Communicate relevant updates to study core team

What you need

Required

• Bachelor's level degree or equivalent in science or health care field

• 2+ years of relevant clinical research experience

• Demonstrated independence in performing site monitoring (e.g. site selection, site initiation, interim monitoring and closeout visits) and site management activities

• Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics

• Ability to apply ISO, FDA and related guidelines toward documentation

Preferred

• Experience as a Clinical Research Coordinator, Clinical Trial Coordinator or Clinical Research Associate

• CCRA Certification

$83,300.00 - $180,400.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

Posting Date: 04/09/2026

Posted Date: 04/09/2026
This role will be posted for a minimum of 3 days.