Full-Time

Clinical Research Coordinator 1

Posted on 1/31/2026

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Boca Raton, FL, USA

In Person

Category
Biology & Biotech (2)
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Requirements
  • Bachelor’s degree in relevant field required
  • Minimum 1 year 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.
Responsibilities
  • 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 deviations and unanticipated occurrences.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Knows the contents and maintenance of study-specific clinical research regulatory binders.
  • 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.
  • Assist the PIs in developing UM protocols for submission to IRB, including but not limited to the submission of required documentation to the UM/JMH IRB to ensure successful approval of research protocols. Maintenance of any reporting and other requirements by the IRB.
  • Administer informed consent forms for patients on drug studies.
  • Develop, review and submit required documentation to the UM/JMH IRB to ensure successful approval of research protocols. Maintain any reports and other requirements by the IRB.
  • Interact with various sponsoring agencies and their representatives, on issues regarding on-going protocols requiring occasional visits to supporting agencies and national meetings. Relate information back to the Division.
  • Coordinate patient recruitment and screening procedures in inpatient and outpatient settings. Obtain necessary medical records, schedule patients for pre-study screening, and maintain a study patient list.
  • Coordinate research related activities between departments to accomplish goals of studies
  • Develop and manage the following procedures as they pertain to research studies and patients:
  • Perform necessary study evaluations
  • Complete patient data forms; collect results from outside laboratories, etc. and complete data into case report forms.
  • Maintain pool of study candidates and ensure their availability.
  • Contact patients by telephone as required by the PI for clinical follow-up for requirements and adherence to research protocols.
  • Complete the medical chart and log-in of patient’s vital signs, including weight, temperature, pulse rate, respiratory rate and blood pressure into case reports.
  • Collect vital signs, lab specimens (blood, urine, etc.)
  • Prepare lab samples for shipping
  • Coordinate the necessary testing for patient evaluations per physician’s orders and study protocol requirements.
  • Process and ship lab specimens to central lab as required by protocol and maintain updated study kits and supplies and maintain general laboratory supplies.
  • Offer assistance and provide information to help patients with protocol procedures.
  • Assist in keeping accurate records of concomitant medications and study medications as per study protocol requirements.
  • Maintain patients chart with clinic notes; up to date reports of laboratory results and change in treatment.
  • Perform other duties as assigned by PI within established policy.

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