Program Coordinator RN - MUSCP

MUSC

Summerville, SCFull-time

Behavioral Health Market Context

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Job Description

h Research

Pay Rate Type
Salary

Pay Grade
Health-29

Scheduled Weekly Hours
40

Work Shift

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

Bachelor’s degree in nursing required and three years related nursing experience in specialty area. Licensure as a registered nurse by the South Carolina Board of Nursing or a compact state. Some positions require certification as a generalist in a related specialty area by the American Nurses Association (ANA). Licensure as a registered nurse by the South Carolina Board of Nursing or a compact state. Some positions require certification as a generalist in a related specialty area by the American Nurses Association (ANA). Current American Heart Association (AHA) Basic Life Support (BLS) certification or American Red Cross BLS for Healthcare Providers certification is required.

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

Qualifications

  • Bachelor’s degree in nursing required and three years related nursing experience in specialty area
  • Licensure as a registered nurse by the South Carolina Board of Nursing or a compact state
  • Some positions require certification as a generalist in a related specialty area by the American Nurses Association (ANA)
  • Licensure as a registered nurse by the South Carolina Board of Nursing or a compact state
  • Some positions require certification as a generalist in a related specialty area by the American Nurses Association (ANA)
  • Current American Heart Association (AHA) Basic Life Support (BLS) certification or American Red Cross BLS for Healthcare Providers certification is required

Benefits

  • Pay Rate Type
  • Pay Grade

Responsibilities

  • Serve as a Program Coordinator - RN and provide comprehensive clinical, regulatory, and program coordination support for human subject's research conducted under the direction of the Principal Investigator (PI) and Program Manager
  • Scheduled Weekly Hours
  • 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


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