Clinical Research Coordinator: Drive Study Operations

Stanford Reglab; Palo Alto (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

Stanford Radiology is seeking a Clinical Research Coordinator Associate to coordinate clinical studies, including participant recruitment, consent, visits, data collection, and regulatory activities. You will work under the principal investigator and/or clinical research supervisor, potentially coordinating assigned activities within established protocols.

Ideal candidates have 1–2 years in clinical research, strong organizational and communication skills, and familiarity with GCP/HIPAA

Qualifications

• 1–2 years of experience in clinical research or a related role.
• Strong organizational, communication, and interpersonal skills.
• Familiarity with GCP, HIPAA, and applicable clinical research regulations.

Responsibilities

• Serve as primary contact with participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout.
• Determine eligibility and obtain consent per protocol. Assist in developing recruitment strategies.
• Coordinate collection of study specimens and processing.

Skills

Clinical research

GCP knowledge

HIPAA knowledge

Communication

Interpersonal skills

Education

Associate or Bachelor’s in related field

Tools

Microsoft Office

Job description

Stanford Radiology is seeking a Clinical Research Coordinator Associate to coordinate clinical studies, including participant recruitment, consent, visits, data collection, and regulatory activities. You will work under the principal investigator and/or clinical research supervisor, potentially coordinating assigned activities within established protocols.

Ideal candidates have 1–2 years in clinical research, strong organizational and communication skills, and familiarity with GCP/HIPAA