Clinical Research Coordinator - $53K-75K per year
Company: University of Miami
Location: Hialeah
Posted on: January 24, 2023
Job Description:
University of Miami is seeking a Clinical Research Coordinator
for a job in Miami, Florida.Job Description & Requirements
- Specialty: Clinical Research Coordinator
- Discipline: Allied Health Professional
- Start Date: ASAP
- Duration: Ongoing
- 40 hours per week
- Shift: 8 hours, days
- Employment Type: PermanentThe Department of Obstetrics and
Gynecology has an exciting opportunity for a Full-Time Clinical
Research Coordinator 3 to work on the UHealth Campus. The Clinical
Research Coordinator 3 serves as an experienced clinical research
professional responsible for providing leadership in the planning,
implementing, monitoring, and evaluating of multiple clinical
research protocols. This role manages multiple studies' daily
operations, carries out study coordination duties from protocol
development and initiation to study close-out according to
regulatory/sponsor guidelines, assures each study's integrity, and
mentors less experienced Clinical Research Coordinators. The
incumbent monitors and maximizes adherence to research standards
and regulatory guidelines and approved operational procedures,
works closely with study team members and other staff/faculty/study
sites to ensure study participant safety and adherence to approved
protocols, manages study-related administrative and human resources
tasks, facilitates across-the-board flow of information, and
orchestrates study activities and personnel.Coordinates the
implementation of multiple complex clinical research
protocols.Develops SOPs and templates with guidance from the
PI/Clinical Research Manager.Oversees and facilitates eligibility
screening and study recruitment activities; implements strategies
to increase accrual.Manages sample processing, packing, and
shipping according to protocol, applicable standards, and
regulations.Plans and operationalizes strategies to monitor,
document, report, and follow-up on unanticipated occurrences and
protocol deviations. Develops and implements preventive/corrective
actions.Develops, disseminates, and assures adherence to
study-related clinical research best practices/scientific
manuals.Assumes leadership in protocol implementation and study
progress, keeping investigators apprised of study progress.Provides
leadership in identifying and working through ethical conflicts
arising during protocol implementation and refers these conflicts
to the Research Ethics Team for consults as needed.Coordinates the
compilation of information needed for research reports;
peer-reviewed publications; develops strategies to disseminate
information to clinical personnel, professional audiences and
stakeholders.Assist PIs and study team with regulatory IRB
submissions, continuing reports, and modifications of protocols,
including maintaining delegation of authority logs, deviation logs,
adverse event logs for all studies.Assists PIs and study team with
screening, recruitment, including informed consent of participants
per protocol guidelines.Assists PIs and study team with scheduling
and contacting study participants for appointments as
needed.Assists PIs and study team with data collection, data entry
and completing standard operating procedures for quality assurance
reviews of data as needed.Assists PIs and study team with
monitoring and tracking of study visits per protocol
guidelines.Maintains required CITI Research Certifications and RSQA
education for research support staff as mandated by the University
and Supervisor.Assists PIs and study team with essential
documentation including maintenance of study binders, shadow
records, and record reviews for study specific data collection per
protocols.Assists in the pre-award process for feasibility
assessment, budget, and study start up as needed.Develops,
verifies, and implements procedures to accomplish research
goals.Implements research protocol and monitors participant
adherence to protocol.Maintains database of department, providing
research training and support, ensuring CITI certification and
relevant trainings are up to date.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
requiredMinimum 4 years of relevant experience required, FDA
experience highly desired/preferredCurrent Research Coordinator
certification by the Association of Clinical Research Professionals
or Society of Clinical Research Associates for a minimum of 6
monthsSkill in collecting, organizing and analyzing data.Ability to
recognize, analyze, and solve a variety of problems.Ability to
analyze, organize and prioritize work under pressure while meeting
deadlines.Ability to process and handle confidential information
with discretion.Ability to work independently and/or in a
collaborative environment.Any appropriate combination of relevant
education, experience and/or certifications may be
considered.#Li-TF1The 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.Patient
safety is a top priority. As a result, during the Influenza ("the
flu") season (September through April), the University Of Miami
Miller School Of Medicine requires all employees who provide
ongoing services to patients, work in a location (all Hospitals and
clinics) where patient care is provided, or work in patient care or
clinical care areas, to have an annual influenza vaccination.
Failure to meet this requirement will result in rescinding or
termination of employment.University of Miami Job ID #R100057926.
Pay package is based on 8 hour shifts and 40 hours per week
(subject to confirmation).About University of MiamiThe 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.Benefits
- 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
Keywords: University of Miami, Hialeah , Clinical Research Coordinator - $53K-75K per year, Healthcare , Hialeah, Florida
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