Clinical Research Coordinator 2

University of Miami

Miami (FL)

On-site

USD 50,000 - 70,000

Full time

14 days+

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Benefits offered by this job

Medical benefits

Dental benefits

Tuition remission

Job summary

An educational institution in Miami is seeking a Clinical Research Coordinator 2. The role involves planning and monitoring clinical studies, ensuring participant safety, and adhering to regulatory guidelines. The ideal candidate has a Bachelor's degree and at least 2 years of relevant experience, along with strong organizational and detail-oriented skills. This position offers competitive salaries and a full-time role with comprehensive benefits.

Qualifications

Minimum 2 years of relevant experience required.
Must follow federal guidelines for participant safety.

Responsibilities

Assist in participant recruitment and retention.
Perform study procedures and data collection.
Maintain study compliance and safety protocols.
Monitor study progress and keep investigators informed.

Skills

Attention to detail

Ability to analyze and prioritize

Confidential information handling

Ability to work under pressure

Commitment to values

Collaborative work

Education

Bachelor’s degree in a relevant field

Job description

Overview

Join to apply for the Clinical Research Coordinator 2 role at University of Miami.

The University of Miami/UHealth Department of SCCC- CRS has an exciting opportunity for a Full‑Time Clinical Research Coordinator 2 to work at the UHealth campus in Miami, FL.

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet.

Core Job Summary

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‑board flow of information, and coordinate study activities and personnel.

Core Responsibilities

Assists in participant recruitment and retention activities and screens 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.

Core Qualifications

Education: Bachelor’s degree in a relevant field required.

Experience: Minimum 2 years of relevant experience required.

Knowledge, Skills and Abilities:

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.

Benefits & Eligibility

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

The University of Miami is an Equal Opportunity Employer – Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.

Job Attributes