UNIV - Research Program Coordinator I - Surgery: Transplant Surgery Research
Company: Medical University of South Carolina
Location: Charleston
Posted on: April 4, 2026
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Job Description:
Job Description Summary The Clinical Research Coordinator is
responsible for conducting all aspects of clinical drug and device
trials; patient data; and disease registries for the Department of
Surgery as directed by the Principal Investigator. This person will
also conduct all research in adherence with the FDA Code of Federal
Regulations, "Good Clinical Practices”, and adhere to the MUSC IRB
regulations for the protection of human subjects. Entity Medical
University of South Carolina (MUSC - Univ) Worker Type Employee
Worker Sub-Type? Research Grant Cost Center CC001066 COM SURG
Administration CC Pay Rate Type Hourly Pay Grade University-GEN08
Pay Range 45,300.00 - 61,100.00 - 77,000.000 Scheduled Weekly Hours
40 Work Shift Job Description Pay Range: $45,300.00 - $61,100.00 -
$77,000.00 Job Duties: 25% - Maintains subject level documentation
for all studies independently. Conducts and assist with study
visits and may perform research assessments. Extracts data from
EPIC. Completes all required case report forms in accurately,
completely, and in a timely manner. Ensure study-required clinical
elements and tests are conducted and collected according to the
protocol. Coordinates with research physicians, raters, and other
study staff for timely completion of all study activities and
ensures all resource areas are available for completion of study
visits. 20% - Supervise and manage day to day clinical trial
operations. Schedules study participants, caregivers, and research
personnel for study visits in compliance with study protocol.
Transcribes data into case report forms completely and accurately.
Monitors completeness and accuracy of case report forms, and
coordinates collection and filing of all source documents. Performs
data entry as per study protocol. 15% - Independently creates
regulatory submissions and annual reports to the IRB and completes
required supplemental regulatory documents for all studies.
Completes IRB and/or Sponsor reportable events independently.
Applies protocol and institutional guidelines to differentiate
between reportable vs. non-reportable adverse events 15% -
Independently obtain and document informed consent. Maintain
accurate informed consent documents for later review. Recruits
study participants per study inclusion and exclusion criteria. 15%
- Prepare for and conduct monitor and auditor visits for each study
as required by sponsor, FDA, etc. Coordinates monitoring visits and
completes corrections and queries in a timely manner. Assists other
study teams as needed to meet study requirements and organizational
goals. 10% - On-call responsibilities on a rotational basis with
others in the department. Will be a resource for all clinical needs
and available to answer study related questions or talk with
patients about study participation. Travel to Sponsor initiated
investigator meetings with investigators. Attend information and
training sessions at investigator meetings to ensure compliance
with study protocol requirements. Preferred Skills: Must be able to
work independently with minimal supervision. Must exercise judgment
and discretion and establish and maintain effective working
relationships. Must be able to communicate effectively. Additional
Job Description Minimum Requirements: A bachelor's degree and two
years of relevant program experience. Physical Requirements: (Note:
The following descriptions are applicable to this section:
Continuous - 6-8 hours per shift; Frequent - 2-6 hours per shift;
Infrequent - 0-2 hours per shift) Ability to perform job functions
in an upright position. (Frequent) Ability to perform job functions
in a seated position. (Frequent) Ability to perform job functions
while walking/mobile. (Frequent) Ability to work indoors.
(Continuous) Ability to work outdoors in all weather and
temperature extremes. (Infrequent) Ability to work in
confined/cramped spaces. (Infrequent) Ability to perform job
functions from kneeling positions. (Infrequent) Ability to squat
and perform job functions. (Infrequent) Ability to perform
'pinching' operations. (Infrequent) Ability to fully use both
hands/arms. (Frequent) Ability to perform repetitive motions with
hands/wrists/elbows and shoulders. (Frequent) Ability to reach in
all directions. (Frequent) Possess good finger dexterity.
(Continuous) Ability to maintain tactile sensory functions.
(Continuous) Ability to lift and carry 15 lbs., unassisted.
(Infrequent) Ability to lower objects, up to 15 lbs., from height
of 36 inches to floor level, unassisted. (Infrequent) Ability to
push/pull objects, up to 15 lbs., unassisted. (Infrequent) Ability
to maintain 20/40 vision, corrected, in one eye or with both eyes.
(Continuous) Ability to see and recognize objects close at hand.
(Frequent) Ability to see and recognize objects at a distance.
(Frequent) Ability to determine distance/relationship between
objects; depth perception. (Frequent) Good peripheral vision
capabilities. (Continuous) Ability to maintain hearing acuity, with
correction. (Continuous) Ability to perform gross motor functions
with frequent fine motor movements. (Frequent) If you like working
with energetic enthusiastic individuals, you will enjoy your career
with us! The Medical University of South Carolina is an Equal
Opportunity Employer. MUSC does not discriminate on the basis of
race, color, religion or belief, age, sex, national origin, gender
identity, sexual orientation, disability, protected veteran status,
family or parental status, or any other status protected by state
laws and/or federal regulations. All qualified applicants are
encouraged to apply and will receive consideration for employment
based upon applicable qualifications, merit and business need.
Medical University of South Carolina participates in the federal
E-Verify program to confirm the identity and employment
authorization of all newly hired employees. For further information
about the E-Verify program, please click here:
http://www.uscis.gov/e-verify/employees
Keywords: Medical University of South Carolina, Savannah , UNIV - Research Program Coordinator I - Surgery: Transplant Surgery Research, Science, Research & Development , Charleston, Georgia