Research Coordinator Associate

7 days ago


Stanford, California, United States Stanford University Full time
Job Summary

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator Associate to join our team at Stanford University. The successful candidate will be responsible for coordinating clinical trials, managing research data, and ensuring compliance with regulatory requirements.

Key Responsibilities
  • Coordinate clinical trials from start-up to close-out, ensuring timely completion and compliance with regulatory requirements.
  • Manage research data, including patient and laboratory data, and ensure accuracy and completeness.
  • Develop and implement recruitment strategies to identify and enroll eligible participants.
  • Collaborate with principal investigators, research staff, and sponsors to ensure smooth trial operations.
  • Monitor and report on trial progress, identifying and addressing any issues or concerns.
  • Ensure compliance with Institutional Review Board (IRB) regulations and other regulatory requirements.
  • Develop and maintain study-related documents, including case report forms and study protocols.
  • Participate in monitor visits and regulatory audits to ensure trial integrity.
Requirements
  • Bachelor's degree in a related field or equivalent combination of education and experience.
  • Two years of experience in clinical research coordination or a related field.
  • Strong knowledge of clinical research principles and regulatory requirements.
  • Excellent communication and interpersonal skills.
  • Ability to work independently and as part of a team.
Preferred Qualifications
  • Clinical research operations certificate or interest in working toward one.
  • Valid California driver's license.
Working Conditions

This is an onsite role that may require working with hazardous materials and exposure to chemicals, blood, body fluids, or tissues, and risk of exposure to contagious diseases and infections.



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