Clinical Research Coordinator 2 - Full Time - Bascom Palmer Eye Institute, Miami

University of Miami

Miami, Florida, US
Competitive salary; comprehensive benefits includi...
Not specified (assumed to be in-person given the nature of the clinical research role).
Minimum 2 years relevant experience
Bachelor's degree in relevant field
Ability to work evenings nights weekends
The University of Miami's Bascom Palmer Eye Institute is seeking a full-time Clinical Research Coordinator 2 responsible for planning, coordinating, and implementing clinical research studies. The ideal candidate should have a bachelor's degree and at least two years of relevant experience, demonstrating skills in detail-oriented tasks, participant recruitment, and adherence to regulatory standards

Job Summary

  • The Clinical Research Coordinator 2 serves as a mid-level professional assisting in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies at Bascom Palmer Eye Institute.
  • This role requires the incumbent to perform study procedures, collect and process specimens, manage regulatory files, and ensure strict adherence to approved protocols and sponsor guidelines.
  • The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission, and more for this full-time staff position.

Matching Summary

Match Score: 85

The University of Miami's Bascom Palmer Eye Institute is seeking a full-time Clinical Research Coordinator 2 responsible for planning, coordinating, and implementing clinical research studies. The ideal candidate should have a bachelor's degree and at least two years of relevant experience, demonstrating skills in detail-oriented tasks, participant recruitment, and adherence to regulatory standards.

Salary

Competitive salary; Comprehensive benefits including medical, dental, tuition remission; Not specified

Skills & Requirements

Must-have

  • Minimum 2 years relevant experience
  • Bachelor's degree in relevant field
  • Ability to work evenings nights weekends
  • Process confidential information with discretion
  • Adhere to international national local regulations

Nice-to-have

  • Commitment to University core values
  • Ability to work independently collaboratively
  • Experience with multiple clinical trials
  • Strong attention to detail accuracy
  • Effective communication with sponsors investigators

Key Requirements

  • Bachelor's degree in relevant field
  • Minimum 2 years of relevant experience
  • Knowledge of regulatory bodies and IRB requirements
  • Ability to handle multiple principal investigators

Work Rights

Not specified

Tailored Resume

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