Clinical Research Coordinator Associate - Trial Operations

Stanford University School of Medicine; Palo Alto (CA); On-site; USD 48,000 - 55,000; Full time

Job summary

Stanford University School of Medicine in Palo Alto seeks a Clinical Research Coordinator Associate to manage multiple protocols, ensure regulatory compliance, and support IRB submissions and amendments.

You will recruit and screen participants, collect data, manage samples, and maintain documentation per HIPAA and GCP guidelines. Occasional evening/weekend hours may be required. Stanford offers a comprehensive benefits program.

Qualifications

• Two year college degree or Bachelor’s degree in a related field or an equivalent combination of education and experience.
• Strong interpersonal skills and communication abilities.
• Familiarity with medical terminology and HIPAA regulations.

Responsibilities

• Serve as primary contact with research participants, sponsors, and regulatory bodies; coordinate studies from startup through close-out.
• Determine eligibility and obtain informed consent; assist in recruitment strategies.

Skills

Interpersonal skills

Microsoft Office

Medical terminology

Education

Two year college degree

Bachelor’s degree in related field

Tools

Microsoft Office

Job description

Stanford University School of Medicine in Palo Alto seeks a Clinical Research Coordinator Associate to manage multiple protocols, ensure regulatory compliance, and support IRB submissions and amendments.

You will recruit and screen participants, collect data, manage samples, and maintain documentation per HIPAA and GCP guidelines. Occasional evening/weekend hours may be required. Stanford offers a comprehensive benefits program.