Clinical Research Coordinator - $46K-65K per year
Company: University of Miami
Location: Hialeah
Posted on: March 12, 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: PermanentDominion TowerThe Department of
Clinical Translational Research Site has an exciting opportunity
for a Full Time Clinical Research Coordinator 2. The Clinical
Research Coordinator 2 serves as a mid-level clinical research
professional that assists in the planning, coordinating,
implementing, monitoring, and evaluating of specific clinical
research studies. This role assists in the day-to-day operations of
clinical research protocol implementation, and carries out study
coordination duties from protocol initiation to study close-out
according to regulatory/sponsor guidelines. The incumbent works
closely with study team members and other staff/faculty/study sites
to ensure study participant safety and adherence to approved
protocols, help with study-related administrative tasks, facilitate
across-the-board flow of information, and coordinate study
activities and personnel.JOB FUNCTIONS Provides professional level
support for research studies. Implements research protocol and
monitors participant adherence to protocol. Establishes
patient/participant screening procedures. Determines data to be
collected and develops forms for collections/summarizing data.
Establishes and maintains contact with patient/participants, health
care providers, community agencies, study sponsors.Provides
professional level support for research studies and assists in the
design of studies.Develops, verifies and implements procedures to
accomplish research goals.Implements research protocol and monitors
participant adherence to protocol.Verifies accuracy of research
data and monitors data quality control.Works together with the
Regulatory Specialist to ensure compliance.Establishes
patient/participant screening procedures with Principal
Investigator and obtains relevant medical information from patient
clinic charts/medical records.Maintains logs/progress reports to
track both currently enrolled as well as follow-up
patients/participants.Maintains drug accountability records for
study drugs.Determines data to be collected and develops forms for
collecting/summarizing data.Maintains and assists clinical research
computer database and enters data onto case reports and/or into
database as appropriate. Ensures data integrity and consistency in
computer database and written records.Completes corrections/queries
required at audits/monitor visits and takes action to correct
deviations as needed.Establishes/maintains contact with
patient/participants, health care providers, community agencies and
study sponsors.Updates appropriate agencies (such as sponsors, IRB,
etc.) regarding current status of research project.Provides
in-service education to staff and patients/participants about
research protocols.Assists in participant recruitment and retention
activities, and assists in screening potential study participants
for eligibility.Performs study procedures, routine tests, data
collection/recording, and daily operations of moderate risk
clinical research protocols.Collects, processes, packs, and ships
specimens according to protocol, applicable standards and
regulations.Maintains study binders and filings according to
protocol requirements, UM and department policy.Distributes study
drug materials according to practice standards and clinical
credentials as delegated by the Principal Investigator.Monitors,
documents, reports, and follows-up on study unanticipated/adverse
events and protocol deviations.Assists in implementing protocol
amendments under direct supervision of the Principal
Investigator.Assists with study orientation and protocol related
in-services to research team and clinical staff.Monitors protocol
implementation and study progress; keeps investigators fully
apprised of study progress; submits progress reports according to
established schedule.Learns the research team and assists with
communications/interactions with sponsor, data coordinating
centers, compliance monitors, collaborators, investigators'
academic administrative personnel, and departments.Assists in
administrative tasks of study personnel including orientation,
documenting core competencies, certification mandates,
safety/responsible conduct of research education, and performance
reviews.Adheres to cultural competency guidelines; implements
strategies to meet study participants' needs for language
translation, health literacy, etc.Follows the appropriate
fundamental requirements of all international, national, and local
regulatory bodies. 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.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
Education:Bachelor's degree in relevant field
required.Certification and Licensing:Clinical Research
Certification, preferred.Experience: Minimum Two (2) years of
relevant experience. Three (3) years of relevant work experience in
clinical trials management or research experience in clinical trial
setting.Knowledge, Skills and Attitudes: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.Any
appropriate combination of relevant education, experience and/or
certifications may be considered.#LN-AL1The 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 #R100061258.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 - $46K-65K per year, Healthcare , Hialeah, Florida
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