Program Coordinator - West Ashley Pediatrics - MUSCP

Medical University of South Carolina; Charleston (SC); Hybrid; USD 42,000 - 54,000; Full time

Job summary

Medical University of South Carolina in Charleston, SC seeks a Program Coordinator I to support the Program Manager, Principal Investigators, and research staff in coordinating human subject activities under supervision. You will participate in day-to-day clinical research operations and serve as a liaison across stakeholders, applying regulatory knowledge to action plans.

Responsibilities include site management, study implementation, participant recruitment, scheduling visits, data collection,

Qualifications

• Bachelor's degree and one year work experience; or high school diploma (or equivalent) and 2 to 4 years work experience.

Responsibilities

• Site management and coordinating study implementation of clinical trials.
• Recruitment of study participants and scheduling study visits.
• Data collection, lab collection and processing, and maintaining regulatory files.
• Liaison for the study across stakeholders; apply research best practices and regulations.

Education

Bachelor's degree and one year work experience; or high school diploma and 2-4 years work experience

Job description

Job Description Summary

Serve as a Program Coordinator I who provides technical and professional services within MUSC Children’s Health. The position will assist the Program Manager, the Principal Investigators (PI), and other research assistants involved in the coordination of human subject activities as delegated by the Program Manager and PI.

Entity

MUSC Health Partners (MHP)

Worker Type

Employee

Worker Sub-Type

Regular

Cost Center

CC005521 CFC PC PEDS MUSC Children's Health Research

Pay Rate Type

Hourly

Pay Grade

Health-24

Scheduled Weekly Hours

40

Job Description

This position will participate in the day-to-day operations in clinical research and perform job duties under general supervision. They will perform a variety of research assessments and serve as a liaison for the study across stakeholders. They will have an in-depth knowledge and understanding of research best practices and regulations, and they will have the ability to apply these concepts in order to determine action plans.

Responsibilities include site management and navigating study implementation of clinical trials, recruitment of study participants, scheduling study visits, data collection, lab collection and processing, conducting research protocols and assessments, and maintaining up to date regulatory files.

This position will be required to work on-site but will be eligible to work from at other times. May be required to work weekends.

Additional Job Description

Education & Experience: A Bachelor's degree and one year work experience; or high school diploma (or equivalent) and 2 to 4 years work experience.

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