Research Protocols
ClinicalResearchCoordinator1(A)FullTime
Neural analysis suggests this role is
optimal for Entry candidates.
“Clinical Research Coordinator 1 (A) Full Time at Research Protocols. Skills: Data management, Clinical research protocols, Patient coordination. Perform chart review/pre-screening. Coordinate simple clinical research protocols”
Industry & Context.
Problem solves when operational failures occur; Helps problem solve protocol deviations; Helps problem solve unanticipated occurrences
Flexibility to travel to all BPEI sites as needed, Ability to work evenings, nights, and weekends as necessary
What They're Looking For.
Must Have
Bachelor’s degree, 1 year of relevant experience, Skill in completing assignments accurately, Ability to analyze, organize and prioritize work, Ability to process and handle confidential information, Ability to work evenings, nights, and weekends, Commitment to the University’s core values, Ability to work independently, Ability to work in a collaborative environment
Nice to Have
Flexibility to travel to all BPEI sites, Ability to handle multiple clinical trials, Serve as back up coordinator
What You'll Do.
Perform chart review/pre-screening
Coordinate simple clinical research protocols
Maintain enrollment procedures
Coordinate routine clinical studies activities
Perform research tests/experiments
Adapt procedures for quality improvement
Operate clinical research equipment
Problem solve operational failures
Observe and inform PI/supervisor of adverse events
Address adverse events per protocol
Advocate for study participants
Identify protocol deviations
Report protocol deviations
Problem solve unanticipated occurrences
Follow fundamental requirements of regulatory bodies
Maintain study-specific regulatory binders
Maintain requisite skills and training
Adhere to University policies
Safeguard University assets
Establish patient/participant screening procedures
Obtain relevant medical information
Handle multiple clinical trials
Serve as back up coordinator
Complete corrections/queries at audits
Take action to correct deviations
Establish/maintain contact with patient/participants
Establish/maintain contact with health care providers
Establish/maintain contact with community agencies
Establish/maintain contact with study sponsors
Update agencies regarding research project status
Provide in-service education to staff
Provide in-service education to patients/participants
Prepare annual reviews for IRB
Submit annual reviews to IRB
Maintain consent forms
Maintain sponsor correspondences
Notify IRB of protocol amendments
Notify IRB of safety reports
Notify IRB of serious adverse events
Implement research protocol
Monitor participant adherence to protocol
How You'll Work.
Team & Collaboration
Ability to work in a collaborative environment
Process & Methodology
Planning study timelines, Planning study schedules
Full Job Description
**_Current Employees:_** If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click [here](https://www.myworkday.com/umiami/d/task/1422$7248.htmld) 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](https://my.it.miami.edu/wda/erpsec/tipsheets/ER_eRecruiting_ApplyforaJob.pdf). The University of Miami, Bascom Palmer Eye Institute, has an exciting opportunity for a Clinical Research Coordinator 1 with Bascom Palmer Eye Institute in Miami, Florida. The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines. **CORE JOB FUNCTIONS** * Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol. * Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation. * Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision. * Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur. * Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants. * Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study. * Identifies, reports, and helps problem solve protocol deviati
Applying for this Clinical Research Coordinator 1 (A) Full Time role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about Research Protocols?
Real rants from real employees. Read before you apply.