Ophthalmology Clinical Research Coordinator II

umiami

Miami (FL)

On-site

USD 65,000 - 90,000

Full time

14 days+
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Job summary

The Bascom Palmer Eye Institute in Miami seeks a full-time Clinical Research Coordinator 2 to support the McKnight Vision Research Center. As a mid-level professional, you will assist in planning, coordinating, implementing, monitoring, and evaluating clinical studies, ensuring participant safety and regulatory compliance while handling data, specimens, and study documentation.

Responsibilities include recruitment, consent, data entry, specimen handling, and liaison with sponsors and study sites

Qualifications

  • Bachelor’s degree in a relevant field.
  • Minimum 2 years of relevant clinical research experience.
  • Detail-oriented with accuracy in assignments.
  • Ability to analyze, organize and prioritize work under pressure.
  • Ability to 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.

Responsibilities

  • Assist in participant recruitment and retention and screen potential participants.
  • Perform study procedures, data collection, and daily operations of moderate risk protocols.
  • Collect, process, pack, and ship specimens per protocol.
  • Maintain study regulatory files and documentation.
  • Distribute study drug materials per standards and delegation.
  • Monitor, document, and report adverse events and deviations.
  • Obtain informed consent and schedule visits.
  • Enter data into electronic data capture within timelines.
  • Communicate with sponsors, centers, and regulatory personnel.

Skills

Detail-oriented
Analytical skills
Prioritization under pressure
Discretion with confidential info
Flexible schedule
Independent + team player

Education

Bachelor’s degree in relevant field

Job description

The Bascom Palmer Eye Institute in Miami seeks a full-time Clinical Research Coordinator 2 to support the McKnight Vision Research Center. As a mid-level professional, you will assist in planning, coordinating, implementing, monitoring, and evaluating clinical studies, ensuring participant safety and regulatory compliance while handling data, specimens, and study documentation.

Responsibilities include recruitment, consent, data entry, specimen handling, and liaison with sponsors and study sites

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