Quick Job Search
Company Name:
Job Type:
Job Seeker Tools
Latest Jobs
Job Seeker Tools
Your Saved Jobs
Build Your Professional Profile
Similar Jobs
Thermo Fisher Scientific
Associate II, Manufacturing in Alachua, FL
Crew Member * 10655 in Orlando, FL
Microsoft D365 Architect, Director in Tampa, FL
Customer Service Associate - Temporary in Miami, FL
University of Miami
Sr. Research Assistant - School of Nursing and Health Studies in Coral Gables,, FL
Client Services Coordinator in Boca Raton, FL
Mobile Technical Lead, Healthcare - Manager in Hallandale, FL
Featured Employers
Clinical Research Coordinator 1
Company: University of Miami
Location: Miami, FL
Employment Type: Full Time
Date Posted: 05/24/2022
Expire Date: 07/24/2022
Job Categories: Healthcare, Other
Job Description
Clinical Research Coordinator 1
The Department of Medicine, Division of Gastroenterology has an exciting opportunity for a Full-Time Clinical Research Coordinator 1 to work on the UHealth Campus. The Clinical Research Coordinator 1 will be responsible for working with Principal Investigators (PI) on sponsored research studies, initiate and maintain regulatory paperwork for each study to include IRBs. The candidate will be expected to meet with study monitors and maintain all regulatory documents. The Clinical Research Coordinator 1 will also administer informed consent forms for patients on multiple studies. Hours may fluctuate depending on clinic and procedure days, therefore, candidate must be flexible in hours.
Coordinate all aspects of ongoing clinical research studies including but not limited to: scheduling and maintaining study patient calendars.
Administer informed consent forms for patients.
Work with CRIS office in the budgeting and negotiating of studies.
Review all expenditures that are to hit the studies for accuracy.
Coordinate patient recruitment and screening procedures in inpatient and outpatient settings.
Obtain necessary medical records, schedule patients for pre-study screening.
Collect results from outside laboratories, etc. and complete data into case report forms
Contact patients by telephone as required by the PI for clinical follow-up regarding requirements and completion of dietary surveys.
Review the medical chart to complete study information.
Completion and maintenance of all regulatory files, including adverse event reporting, etc.
Collect/draw vital signs and lab specimens (blood, stool, urine, etc).
Keep information up to date on REDCap database.
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.

Bachelor’s Degree in relevant field required, or combination education and experience.
Minimum 1-3 years of relevant experience, or experience working with patients in a clinical setting and/or research setting
Phlebotomy certification or Requires completion of a formal Phlebotomy training program within 30 days of hire.
American Heart Association Approved BLS/CPR
HIV Certification
Must be fluent in Spanish and English.
Skill in completing assignments accurately and with attention to detail.
Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
Ability to process and 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.
Contact Information
Apply Now | Forward Job to a Friend | More Jobs From This Employer