Full-Time

Clinical Research Coordinator 2

A

Posted on 1/31/2026

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (2)
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Requirements
  • Bachelor’s degree in relevant field
  • Minimum 2 years of relevant experience
  • Knowledge, Skills and Attitudes: Skill in completing assignments accurately and with attention to detail
  • Knowledge, Skills and Attitudes: Ability to analyze, organize and prioritize work under pressure while meeting deadlines
  • Knowledge, Skills and Attitudes: Ability to process and handle confidential information with discretion
  • Knowledge, Skills and Attitudes: Ability to work evenings, nights, and weekends as necessary
  • Knowledge, Skills and Attitudes: Commitment to the University’s core values
  • Knowledge, Skills and Attitudes: Ability to work independently and/or in a collaborative environment
Responsibilities
  • 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
  • Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators’ academic administrative personnel, and departments
  • Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews
  • Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc.
  • 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
  • Adheres to University and unit-level policies and procedures and safeguards University assets
  • 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.
Desired Qualifications
  • Bilingual (English and Spanish) preferred.

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INACTIVE