Staff Clinical Research Associate

As Staff Clinical Research Associate you will support clinical studies endtoend gaining experience in site monitoring documentation and compliance while working closely with crossfunctional study teams.

What you will do

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

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

• Ensuresite 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

• Communicaterelevant updates to study core team

What you need

Required

• Bachelors level degree or equivalent in science or health care field

• 4 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

• Experience in Device or Pharmaceutical industry

• CCRA Certification

Posting Date: 05/19/2026