Staff PositionLevel I - Clinical Research Coordinator
$40K-56K/year
Level I - Clinical Research Coordinator
UHealth Tower
Miami, FL
5x8 hrs, Days
$40K-56K/yearPosted 2 days ago
Overview
- Start DateASAP
- Shift Breakdown5x8 hrs
- ShiftDays
- Facility InformationNot-For-Profit HospitalShort Term Acute CareTeaching Institution553 bedsEpic Systems Corporation
Pay
Estimated pay
$40K-56K/yearBenefits
- Holiday Pay
- 403b retirement plan
- Sick pay
- Wellness and fitness programs
- Employee assistance programs
- Medical benefits
- Dental benefits
- Vision benefits
- Benefits start day 1
- Continuing Education
Qualifications
The employer will review your Vivian profile and compare it against the job qualifications listed below.
Required
- Eligible to work in US
Other
Description
IDEA Exchange Trailer 1
Clinical Research Coordinator 1 /Division of Infectious Diseases
The Department of Medicine, Division of Infectious Diseases has an exciting opportunity for a Full Time Clinical Research Coordinator 1 to work in the UHealth Campus. 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 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.
Department Specific Functions
Reports to Principal Investigators, Program Director, and Study Coordinators on assigned funded/unfunded research studies at IDEA Syringe Services Program (SSP) at UM.Assists Principal Investigators in all stages of clinical trial procedures at research sites. Develops and maintains all study-specific reporting needs and requirements as established by the IRB, HSRO, DOH, and the HIPAA office, as well as additional site-related grant report requirements.
Assists with study procedure development and documentation for other clinical trials and IDEA related research as directed by Principal Investigators and Program Director.
Coordinates with various agencies, partners, and lead team investigators on issues regarding future and ongoing protocols & serves as a representative amongst supporting agencies and national meetings involved with participant recruitment.
Assists Principal Investigators to maintain and coordinate all relevant research databases and related activities to ensure accurate data entries, including: record keeping and review (as required by protocols and Florida law), new member training, internal coordination or services and staff, scheduling of participants, and additional administrative activities (petty cash coordination, maintaining participant logs, supply ordering, etc.).
Assists Principal Investigators in the publication of significant results including authorship of scientific monographs and advances expertise through continued education, training, and research.
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
Minimum 1 year of relevant experience
#LI-EL1
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
Clinical Research Coordinator 1 /Division of Infectious Diseases
The Department of Medicine, Division of Infectious Diseases has an exciting opportunity for a Full Time Clinical Research Coordinator 1 to work in the UHealth Campus. 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 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.
Department Specific Functions
Reports to Principal Investigators, Program Director, and Study Coordinators on assigned funded/unfunded research studies at IDEA Syringe Services Program (SSP) at UM.Assists Principal Investigators in all stages of clinical trial procedures at research sites. Develops and maintains all study-specific reporting needs and requirements as established by the IRB, HSRO, DOH, and the HIPAA office, as well as additional site-related grant report requirements.
Assists with study procedure development and documentation for other clinical trials and IDEA related research as directed by Principal Investigators and Program Director.
Coordinates with various agencies, partners, and lead team investigators on issues regarding future and ongoing protocols & serves as a representative amongst supporting agencies and national meetings involved with participant recruitment.
Assists Principal Investigators to maintain and coordinate all relevant research databases and related activities to ensure accurate data entries, including: record keeping and review (as required by protocols and Florida law), new member training, internal coordination or services and staff, scheduling of participants, and additional administrative activities (petty cash coordination, maintaining participant logs, supply ordering, etc.).
Assists Principal Investigators in the publication of significant results including authorship of scientific monographs and advances expertise through continued education, training, and research.
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
Minimum 1 year of relevant experience
#LI-EL1
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
University of Miami Job ID #R100082580.
Facility
UHealth Tower
4.0rating(78 reviews)
5.0rating
Anonymous
Oncology (RN)
Staff Position
Review of UHealth Tower on Dec 9, 2024DetailsVerification data is contributed by healthcare professionals like you, who leave reviews on Vivian.
- Not-For-Profit Hospital
- Short Term Acute Care
- Teaching Institution
- 553 beds
- Epic Systems Corporation
ADDRESS1400 NW 12th AveMiami, FL 33136
View more detailsEmployer
University of Miami
3.7rating(22 reviews)
Compensation
3.3rating
Culture
3.3rating
Work Environment
3.3rating
5.0rating
Anonymous
CNA (CNA)
About
The University of Miami is considered among the top tier institutions of higher education in the U.S. for its academic excellence, superior medical care, and cutting-edge research. At the U, we are committed to attracting a talented workforce to support our common mission of transforming lives through teaching, research, and service. Through our values of Diversity, Integrity, Responsibility, Excellence, Compassion, Creativity and Teamwork (DIRECCT) we strive to create an environment where everyone contributes in making the University a great place to work. We are one of the largest private employers in Miami-Dade County; home to more than 16,000 faculty and staff from all over the world.
Response timewithin a day
Staff jobs$13–105/hour
Local contracts$13–105/hour
Per Diem / PRN roles$13–105/hour
Jobs on Vivian210
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