Clinical Research Coordinator 2 Job

The Sylvester Comprehensive Cancer Center has an exciting opportunity for a Full-Time Clinical Research Coordinator 2 to work on the UHealth Campus. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel.

• Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility.
  


• Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols.
  


• Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations.
  


• Maintains study binders and filings according to protocol requirements, UM and department policy.
  


• Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.
  


• Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
  


• Assists in implementing protocol amendments under direct supervision of the Principal Investigator.
  


• Assists with study orientation and protocol related in-services to research team and clinical staff.
  


• Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.
  


• Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  


• Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

MINIMUM QUALIFICATIONS

• Bachelor's degree in relevant field
  


• Minimum 2 years of relevant experience
  


• Skill in completing assignments accurately and with attention to detail.
  


• Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
  


• Ability to process and handle confidential information with discretion.
  


• Ability to work evenings, nights, and weekends as necessary.
  


• Commitment to the University's core values.
  


• Ability to work independently and/or in a collaborative environment.
  

Any appropriate combination of relevant education, experience and/or certifications may be considered.