Clinical Research Coordinator ; Bascom Palmer Eye Institute Miami, FL

Position: Clinical Research Coordinator 2 (A) Full Time Bascom Palmer Eye Institute Miami, FL
Clinical Research Coordinator 2 (A) Full Time Bascom Palmer Eye Institute Miami, FL page is loaded## Clinical Research Coordinator 2 (A) Full Time Bascom Palmer Eye Institute Miami, FL locations:
Miami, FLtime type:
Full time posted on:
Posted Todayjob requisition :
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** Current Employees:
** If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click  to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this .The University of Miami, Bascom Palmer Eye Institute, has an exciting opportunity for a full time opportunity for a Clinical Research Coordinator 2 in Miami, Florida.

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.
** Core

Job Functions:

*** Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility.
* Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols
* Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations.
* Maintains study binders and filings according to protocol requirements, UM and department policy.
* Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.
* Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.
* Assists in implementing protocol amendments under direct supervision of the Principal Investigator.
* Assists with study orientation and protocol related in-services to research team and clinical staff.
* Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.
* Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators’ academic administrative personnel, and departments.
* Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.
* Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc.
* Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
* Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
* Adheres to University and unit-level policies and procedures and safeguards University assets.

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.
** CORE QUALIFICATIONS
***
* Education:

** Bachelor’s degree in relevant field
*
* Experience:

** Minimum 2 years of relevant experience
** Knowledge, Skills and Attitudes:
*** 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…