Full-Time

Clinical Research Coordinator 2

Posted on 12/30/2025

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

Hybrid

Category
Biology & Biotech (2)
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Requirements
  • Education: Bachelor’s degree in relevant field
  • Experience: 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, and 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.

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Total Funding

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Headquarters

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Founded

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INACTIVE