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Clinical Research Coordinator Associate

2 months ago

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

Stanford University is seeking a highly skilled Clinical Research Coordinator Associate to join our team. As a key member of our research team, you will be responsible for coordinating clinical studies, managing data, and ensuring compliance with research protocols.

Key Responsibilities
  • Study Coordination: Coordinate studies from startup through close-out, ensuring timely completion and accuracy of data.
  • Data Management: Collect, manage, and analyze patient and laboratory data for clinical research projects.
  • Regulatory Compliance: Ensure compliance with research protocols, review and audit case report forms, and prepare regulatory submissions.
  • Communication: Serve as primary contact with research participants, sponsors, and regulatory agencies, ensuring effective communication and resolution of issues.
  • Project Management: Develop and implement recruitment strategies, manage research project databases, and complete study documents/case report forms.
Requirements
  • Education: Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience.
  • Experience: 2 years of related experience in clinical trial coordination.
  • Certifications: Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Working Conditions
  • Work Environment: This position is based in Stanford's Research Park and Stanford main campus and has the option of telecommuting/hybrid schedule subject to operational needs.
  • Physical Requirements: Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping. Occasionally sit, reach above shoulders, perform desk-based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.