Senior Clinical Research Coordinator

2 days ago


San Francisco, California, United States University of California , San Francisco Full time
Job Summary

The University of California, San Francisco (UCSF) is seeking a highly skilled and experienced Senior Clinical Research Coordinator to join our team. As a key member of our research team, you will be responsible for coordinating and managing clinical research studies, ensuring compliance with regulatory requirements, and providing exceptional support to our investigators and research staff.

Key Responsibilities
  • Coordinate and manage clinical research studies, including protocol development, subject recruitment, and data management.
  • Ensure compliance with regulatory requirements, including FDA regulations, IRB guidelines, and UCSF policies.
  • Provide exceptional support to investigators and research staff, including training, guidance, and troubleshooting.
  • Collaborate with cross-functional teams, including research staff, clinicians, and administrative personnel, to ensure seamless study execution.
  • Develop and maintain accurate and detailed study documentation, including study protocols, informed consent forms, and case report forms.
  • Conduct site visits, monitor study progress, and identify and resolve issues in a timely manner.
  • Develop and implement quality control measures to ensure data accuracy and integrity.
  • Stay up-to-date with regulatory requirements, industry trends, and best practices in clinical research.
Requirements
  • Bachelor's degree in a related field, such as biology, chemistry, or a related field.
  • Minimum 3 years of experience in clinical research, including experience with study coordination, data management, and regulatory compliance.
  • Excellent communication, organizational, and problem-solving skills.
  • Ability to work independently and as part of a team.
  • Strong attention to detail and ability to maintain accurate records.
  • Ability to work in a fast-paced environment and prioritize multiple tasks and deadlines.
Preferred Qualifications
  • Master's degree in a related field.
  • Experience with electronic data capture systems and clinical trial management software.
  • Certification in clinical research, such as CCRA or CCRP.
What We Offer

UCSF offers a competitive salary and benefits package, including medical, dental, and vision insurance, retirement savings plan, and paid time off. We also offer opportunities for professional growth and development, including training and education programs.



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