Clinical Research Coordinator 2 (Genitourinary -GU)

University of Miami; Miami (FL); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Tuition remission

Competitive salary

Job summary

University of Miami Health System is seeking a Clinical Research Coordinator 2 for Genitourinary (GU) studies in Miami, FL. This on-site, full-time role supports protocol implementation, participant screening, data collection and regulatory compliance across multiple study sites.

The position requires a bachelor’s degree and at least 2 years of relevant experience, with a focus on collaboration, attention to detail and effective communication with study teams and sponsors.

Qualifications

• Learning agility: adapt to new procedures, priorities and technologies.
• Teamwork: collaborate effectively within a research team.
• Technical proficiency: comfortable with office software and clinical data systems.
• Communication: strong written and verbal skills with stakeholders.

Responsibilities

• Assist in planning, coordinating, implementing and evaluating clinical studies.
• Support day-to-day protocol execution from initiation to close-out.
• Recruit and screen participants for eligibility and retention activities.
• Perform study procedures and routine tests per protocol.
• Process specimens and ensure proper storage, labeling and shipping.
• Maintain and organize study binders and regulatory filings.
• Distribute study materials per PI instructions and credentials.
• Monitor and report adverse events and protocol deviations.
• Assist with protocol amendments under PI supervision.
• Provide orientation and training to study staff and clinical teams.
• Track progress and prepare progress reports for investigators.
• Coordinate communications with sponsors, data centers and collaborators.
• Ensure compliance with safety, ethics and regulatory standards.
• Support training, certifications and performance reviews for staff.

Job description

Clinical Research Coordinator 2 (Genitourinary -GU) - Logo### Clinical Research Coordinator 2 (Genitourinary -GU)Apply: On-Site: Miami, FL: Full time: Posted Today: R100102334**Current Employees:**If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here 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 tip sheet.The University of Miami/UHealth Department of SCCC has an exciting opportunity for a Full-Time Clinical Research Coordinator 2 to work at UHealth in Miami, Florida. **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-the-board flow of information, and coordinate study activities and personnel. **CORE JOB FUNCTIONS**1. Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility.2. Performs study procedures, routine tests, data collection/recording, and daily operations of moderate risk clinical research protocols.3. Collects, processes, packs, and ships specimens according to protocol, applicable standards and regulations.4. Maintains study binders and filings according to protocol requirements, UM and department policy.5. Distributes study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.6. Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocol deviations.7. Assists in implementing protocol amendments under direct supervision of the Principal Investigator.8. Assists with study orientation and protocol related in-services to research team and clinical staff.9. Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.10. Learns the research team and assists with communications/interactions with sponsor, data coordinating centers, compliance monitors, collaborators, investigators’ academic administrative personnel, and departments.11. Assists in administrative tasks of study personnel including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.12. Adheres to cultural competency guidelines; implements strategies to meet study participants’ needs for language translation, health literacy, etc.13. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.14. Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.15. 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 required Experience: Minimum 2 years of relevant experience required Knowledge, Skills and Abilities:* Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.* Teamwork: Ability to work collaboratively with others and contribute to a team environment.* Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.* Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders. This is a core job profile description and is not reflective of all duties that may be assigned to a specific position in each individual department. The above statements are intended to describe the general nature and primary responsibilities of this core job profile. Specific duties and tasks may vary based upon departmental needs. Other duties may be assigned to the above consistent with the knowledge, skills, and abilities required for the job.The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.**Job Status:**Full time**Employee Type:**Staff