Full-Time

Univ – Research Program Assistant

Psychiatry: Addiction Sciences Division

Confirmed live in the last 24 hours

Medical University of South Carolina

Medical University of South Carolina

Compensation Overview

$32.7k - $60.5kAnnually

Entry

Charleston, SC, USA

Position is completely in-person at MUSC Charleston.

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
Data Analysis
Requirements
  • A high school diploma and three years of relevant program experience. A bachelor's degree may be substituted for the required program experience.
  • A bachelor’s degree in psychology, biology, nursing and other natural, life or health care field is preferred.
  • The ability to collect, organize and analyze information in a clear and concise manner is required.
Responsibilities
  • Coordinate and manage the tracking of all research study participants throughout their duration in the study.
  • Educate potential participants on study procedures at screening visit and ensure their consent to participate is informed.
  • Complete screening assessments including a mental health diagnostic interview.
  • Lead participants through visit activities for all study visits, which can occur remotely or in person at the research offices.
  • Coordinate visit needs, which include instructing participants on the conduct and testing of biological samples (urine, saliva, etc.) and collaborating with medical clinicians on studies to ensure safety of study participants and eligibility for the study.
  • Upkeep all databases and calendars used to track and manage study referrals and scheduling.
  • Contact potential participants, complete a prescreen questionnaire, and communicate clear information to participants about the study.
  • Schedule visits on team calendar and coordinate with medical clinician’s schedule as needed.
  • Enter visit and participant data into patient data files including participant study binders, study logs, and electronic databases, all completed in a timely manner and in accordance with good clinical practice guidelines.
  • Maintain accurate and complete study documentation in compliance with Institutional Review Board (IRB) standards and Good Clinical Practice (GCP) guidelines.
  • Verify data entered by other research staff in a timely manner.
  • Assist the Program Manager, Research Coordinators and other members of the research team with recruitment and advertising efforts.
  • Recruitment at in-person events or clinics is required.
  • Flexibility is requested to occasionally work outside of business hours to staff events.
  • Scrutinize on an ongoing basis the effectiveness of study procedures and suggest changes when necessary.
  • Ability to create or make updates to study procedural manuals/guidance documents as needed.
  • Keep track of study supplies and inventory to alert Program Coordinator/Manager when materials are running low.
  • Maintain study equipment (such as study phones, shipping supplies, etc.) by keeping track items, maintaining supplies, etc.
Medical University of South Carolina

Medical University of South Carolina

View

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A