More jobs:
Clinical Research Nurse Miami FL
Job in
Miami, Miami-Dade County, Florida, 33222, USA
Listed on 2026-07-13
Listing for:
University of Miami
Full Time, Seasonal/Temporary
position Listed on 2026-07-13
Job specializations:
-
Nursing
Clinical Research Nurse, RN Nurse
Job Description & How to Apply Below
## Clinical Research Nurse 2 - Full-Time, Miami FLApplyremote type:
On-Site locations:
Miami, FLtime type:
Full time posted on:
Posted Todayjob requisition :
R
** Current Employees:
** If you are a current Staff, Faculty or Temporary employee at the University of Miami, please 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 Clinical Translational Research Site has an exciting opportunity for a full-time Clinical Research Nurse 2 to work on-site in Miami, FL.
** CORE JOB SUMMARY
** The Clinical Research Nurse 2 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures. Additionally, the Clinical Research Nurse 2 plays a key role in the recruitment of participants and achievement of research objectives.
** CORE JOB FUNCTIONS
** 1. Assesses, troubleshoots, and reports problems with data collection to appropriate managing staff.
2. Identifies desired research outcomes and evaluates and monitors subjects’ responses.
3. Conducts initiation visits and registers patients in clinical studies.
4. Performs study data collection and entry using charts, correspondence, medical records, and relevant communications. Identifies and procures equipment and supplies needed to fulfill project requirements.
5. Educates staff and subjects about protocols, treatment, possible side effects, and complications. May also collect and handle specimens as required by individual study protocols.
6. Prepares and processes new research proposals and amendments and continually monitors applications and adverse events.
7. Assists with study completion, data lock, study closeout, and archiving of study files to ensure completeness and continuity of all study data.
8. Completes ongoing checks of clinical data entered on the case report forms to ensure accuracy and revises any discrepancies.
9. 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
*** Bachelor’s degree in relevant field required
* Minimum 3 years of relevant experience required
* Valid State of Florida RN license 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.
** DEPARTMENT ADDENDUM
**** Department Specific Functions
** 1.Work with CTRS lead nurse to ensure that nursing services, policies, and procedures are in alignment with the regulatory and compliance guidelines at institutional and federal levels.
2. Participate in the oversight of participant visit scheduling to ensure adequate coverage.
3. Assist the lead nurse in weekly meetings of clinical research staff to ensure that challenges and issues are addressed promptly and efficiently.
4. Assist with review and updates of SOPS relating to the CTRS as needed.
5. Participate in the onboarding of all new CTRS clinical research nurses and medical assistants
6. Partner with Lead Nurse and participate in CTRS in-service protocol meetings.
7. Maintain required training, credentialing, competencies, and other requirements as specified by MSOM, UHT, JHS, and other relevant entities (including Citi Training, Bio Safety, Lab Safety, OSHA, and HIPAA).8.Participate in quality review to ensure accurate and compliant documentation.
9.Reviews Serious Adverse Events documented and reported per the protocol and regulatory requirements for protocols serviced by the CTRS.
10. Work closely with principal investigators and staff across…
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