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Clinical Research Coordinator 2
Company: University of Miami
Location: Miami, FL
Employment Type: Full Time
Date Posted: 05/20/2022
Expire Date: 07/20/2022
Job Categories: Administrative and Support Services
Job Description
Clinical Research Coordinator 2
Description:
The Department of General Medicine has an exciting opportunity for a Full-Time Clinical Research Coordinator 2 to work on the UHealth Campus. The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel.
In conjunction with research manager implements policies and procedures to accomplish project goals
Established and oversees clinic study flow procedures
Facilitates in the scheduling of appointments for participants and actively monitors recruitment staff schedules for opportunities to schedule appointments
Maintains logs/progress reports to track both currently enrolled as well as follow-up patients/participants
Oversee procedures for collecting, processing and shipping bio-specimens to the designated biobank.
Maintenance and calibrations of study equipment (scales, centrifuges)
Helps prepares patient invoices for payments, repairs, trials, warranties etc.
Helps develop forms for collections/summarizing data.
Providing assistance with IRB processes (e.g., abiding by requirement for reporting safety or study deviations, initiating modifications to study procedures
As needed, assists and serves as a backup in CHW in study related procedures such as informed consent, obtaining survey data and study related examination and serve as a back-up for phlebotomy when needed
Participate in ongoing UM and research related trainings
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.

MINIMUM QUALIFICATIONS
Bachelorís degree in relevant field required
Minimum 2 years of relevant experience
Experience performing phlebotomy preferred
Bilingual (English and Spanish)
Flexible hours may be needed to accommodate the needs of the clients - Some evenings and weekends.
Local traveling involved as well as travel to national meetings and trainings will also be required.
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 independently and/or in a collaborative environment.
Contact Information
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