Clinical Research Coordinator 2 job Miami Florida
Clinical Research Coordinator 2 job Miami Florida
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Clinical Research Coordinator 2 Job



Employer Name: SpiderID: 12523539
Location: Miami, Florida Date Posted: 5/12/2022
Wage: Negotiable Category: Science/Research
Job Code: R100055197

Job Description:

The Sylvester Comprehensive Cancer Center 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.



  • 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.

  • 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.


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



  • Bachelor's degree in relevant field

  • Minimum 2 years of relevant experience

  • 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.


Any appropriate combination of relevant education, experience and/or certifications may be considered.



Job Criteria:
Start Date:
Position Type: Full-Time Permanent
Years of Experience Required:
Education Required:
Overnight Travel:
Vacation Time:


Contact Information:
Contact Name: University of Miami Health System Company Type:
Company: University of Miami Health System
City:
State:
Zip:

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