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Clinical Research Coord , MCVI Research

Job in Coral Gables, Miami-Dade County, Florida, 33114, USA
Listing for: Baptist Health
Full Time position
Listed on 2025-12-01
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 31.65 - 41.15 USD Hourly USD 31.65 41.15 HOUR
Job Description & How to Apply Below
Position: Clinical Research Coord 3, MCVI Research, FT, 8A-4:30P

Clinical Research Coord 3, MCVI Research, FT, 8A-4:30P

Join Baptist Health as a Clinical Research Coord 3, MCVI Research, FT, 8A-4:30P.

Baptist Health is the region’s largest not-for-profit healthcare organization, with 12 hospitals, over 28,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.

What truly sets us apart is our people. At Baptist Health, we create personal connections with our colleagues that go beyond the workplace, and we form meaningful relationships with patients and their families that extend beyond delivering care.

Description

Responsible for supporting the Research leadership and Principal Investigator of a designated research project. Performs those functions required by the research protocols with attention to participant safety. Ensures that all requirements of the protocol are met, while meeting compliance with regulatory standards and FDA requirements for each protocol. Must be able to complete detailed paperwork in strict accordance with regulatory requirements and collaborate with physicians, patients, sponsors, and other departments in a service excellence manner.

Estimated pay range for this position is $31.65 - $41.15 / hour depending on experience.

Qualifications
  • Degree:
    Bachelor’s
Licenses & Certifications
  • Basic Life Support
  • ACRP Certified Clinical Research Coordinator
  • SOCRA Certified Clinical Research Professional
  • Collab Inst Training Init
Additional Qualifications
  • CITI and CCRC or CCRP certifications are required
  • Extensive experience in all aspects of Clinical Trials
  • Advanced computer literacy in Microsoft Office
  • Proven ability to manage multiple assignments systematically
  • Excellent interpersonal, collaborative, and team-building skills are required
  • Must be able to work in a high-demand environment with the ability to take responsibility in meeting deadlines
  • Strong verbal and written communication skills

Minimum

Required Experience:

6 years

EOE, including disability/vets

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