Clinical Research Coordinator Associate — Full Study Lifecycle

Stanford University School of Medicine

Palo Alto (CA)

On-site

USD 65,000 - 82,000

Full time

5 days ago
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Job summary

TheStanford Center for Clinical Research (SCCR) within Stanford University School of Medicine is seeking a one-year fixed-term Clinical Research Coordinator. The role focuses on coordinating studies from startup to closeout, ensuring protocol compliance, and managing regulatory submissions and data workflows.

Ideal candidates have strong interpersonal skills, proficiency with Microsoft Office, and knowledge of medical terminology, with a background in clinical research or related field.

Qualifications

  • Strong interpersonal skills.
  • Proficiency with Microsoft Office.
  • Knowledge of medical terminology.

Responsibilities

  • Serve as primary contact with research participants, sponsors, and regulatory agencies; coordinate studies from start-up through closeout.
  • Determine eligibility of and gather consent from study participants per protocol; assist in recruitment strategies.
  • Coordinate collection of study specimens and processing.
  • Collect and manage patient and laboratory data for clinical research projects; manage study databases and documents.
  • Ensure compliance with protocols; review and audit case report forms with source documents.
  • Prepare regulatory submissions and ensure IRB renewals are completed.
  • Monitor visits, budgeting, and interactions with sponsors; attend monitoring meetings.

Skills

Interpersonal skills
Microsoft Office
Medical terminology

Education

Two-year degree
Bachelor’s degree or equivalent

Job description

TheStanford Center for Clinical Research (SCCR) within Stanford University School of Medicine is seeking a one-year fixed-term Clinical Research Coordinator. The role focuses on coordinating studies from startup to closeout, ensuring protocol compliance, and managing regulatory submissions and data workflows.

Ideal candidates have strong interpersonal skills, proficiency with Microsoft Office, and knowledge of medical terminology, with a background in clinical research or related field.

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