Clinical Trials Coordinator - IRB & Data Management

Abundance Network; United States; On-site; USD 47,000 - 55,000; Full time

Job summary

Stanford University is seeking a Clinical Research Coordinator Associate to manage multiple protocols at Stanford Hospital and Clinics. Assist with IRB submissions, informed consent, data collection, and regulatory compliance.

Interact with investigators, sponsors and subjects to ensure safety and proper conduct of clinical trials. The role requires a two-year degree with related experience or a Bachelor's degree, strong interpersonal skills, and familiarity with medical terminology.

Qualifications

• Two year college degree with two years related experience, or a Bachelor's degree in a related field.
• Strong interpersonal skills and knowledge of medical terminology.
• Certification preferred: SCCA or ACRP.

Responsibilities

• Serve as primary contact with research participants, sponsors, and regulatory agencies.
• Coordinate studies from startup through close-out.
• Determine eligibility and obtain informed consent from participants.
• Collect and manage patient and laboratory data, and maintain study documents.
• Ensure compliance with protocols and prepare regulatory submissions.

Skills

Strong interpersonal skills

Microsoft Office

Medical terminology

Education

Two year college degree with two years related experience or Bachelor's degree in a related field

Job description

Stanford University is seeking a Clinical Research Coordinator Associate to manage multiple protocols at Stanford Hospital and Clinics. Assist with IRB submissions, informed consent, data collection, and regulatory compliance.

Interact with investigators, sponsors and subjects to ensure safety and proper conduct of clinical trials. The role requires a two-year degree with related experience or a Bachelor's degree, strong interpersonal skills, and familiarity with medical terminology.