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Clinical Research Coordinator Associate

2 months ago

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

We are seeking a highly motivated and organized Clinical Research Coordinator Associate to join our team in the Division of Cardiovascular Medicine at Stanford University. The successful candidate will be responsible for coordinating clinical trials, managing research projects, 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 projects, including data collection, data management, and data analysis.
  • Develop and implement recruitment strategies to ensure adequate participant enrollment.
  • Collaborate with principal investigators, research staff, and sponsors to ensure successful trial execution.
  • 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.
  • Coordinate with finance and management staff to ensure accurate budgeting and financial management.
  • Participate in monitor visits and regulatory audits to ensure compliance with regulatory requirements.
Requirements
  • Bachelor's degree in a related field or equivalent combination of education and experience.
  • 1-2 years of experience in clinical research coordination or a related field.
  • Strong organizational and communication skills.
  • Ability to work independently and as part of a team.
  • Proficiency in Microsoft Office and other research-related software.
Working Conditions

This position may require occasional evening and weekend hours, as well as work in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.