Job Description Summary
Program Coordinator will provide technical and clinical support for research studies with the Division of Pulmonary and Critical Care for the Department of Medicine.Entity
Medical University of South Carolina (MUSC - Univ)Worker Type
EmployeeWorker Sub-Type
Research GrantCost Center
CC000974 COM DOM PULM General CCPay Rate Type
HourlyPay Grade
University-GEN08
Pay Range
Scheduled Weekly Hours
40Work Shift
Day (United States of America)Job Description
Job Duties:
35% - Program Coordinator will be responsible for the management of subject recruitment and enrollment to assigned research studies. Duties will include creating and adapting recruitment and advertising materials, recruitment tracking, and independently screening subjects. The Program Coordinator will review patient medical records to identify subjects who qualify for actively enrolling studies. Program Coordinator will independently consent subjects for assigned studies in adherence to human subjects’ protection regulations. Program Coordinator will schedule study visits and conduct assessments of study procedures per study protocol. Program Coordinator will be responsible for the preparation, collection, processing, and shipment of biological research specimens. Program Coordinator will assist with management of investigational products and will be responsible for the coordination of the IP with investigational pharmacies. Program Coordinator will coordinate the reporting of adverse events to appropriate entity.
30% - Program Coordinator will be responsible for routine and complex data collection and data entry as well as query resolution. Program Coordinator maintains current and long-term follow-up data on all assigned study subjects. Program coordinator is responsible for the creation, development, and management of simple online databases (MUSC RedCap, etc). Program Coordinator is responsible for the creation of complex data collection forms (CRFs and source documents) according to the study protocol.
20% - Program Coordinator is responsible for the regulatory management of assigned research studies. Program Coordinator will maintain regulatory and training documents as required by Federal, State, local, Institutional and protocol regulations and policies. Program Coordinator will maintain accurate study registration on (Clinicaltrial.gov, etc.). Program Coordinator will serve as primary liaison with the IRB for assigned studies and be responsible for initial study application submission, continuing reviews, amendments, and protocol deviations.
10% - Program Coordinator will directly interact with site personnel and principal investigators, including those at remote sites participating in multi-site trials or tele-medicine programs, thereby requiring effective communication skills, both written and verbal. As part of research team, Program Coordinator will participate in team meetings and provide study updates as required. Program Coordinator will communicate and coordinate with other research personnel as required for study implementation and routine problem resolution.
5% - Program coordinator will regularly review study financial records to ensure accurate billing and resources assigned to each study. Program Coordinator will prepare for study monitoring visits and audits and assist with addressing findings.
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
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