Research Assistant

1 day ago


Charlotte, North Carolina, United States IQVIA Full time
Job Title: Clinical Trials Specialist

The primary role of this position is to assist in the conduct of clinical trial activities, adhering to all applicable regulations. The ideal candidate will possess strong logical thinking skills, ability to prioritize tasks, and excellent interpersonal skills.

Schedule and Work Environment:

This is a 24-hour per week on-site position. We are seeking an individual who can work effectively in a team environment and establish strong working relationships with study team members, investigators, and office staff.

Responsibilities:
  • EDC entry and query resolution
  • Developing strong working relationships and maintaining effective communication with study team members
  • Building trust and respect between the clinic and research office through effective communication
  • Assisting with screening, recruiting, and enrolling research subjects
  • Patient/research participant scheduling
  • Collecting patient/research participant history
  • Coordinating follow-up care and laboratory procedures
  • Adhering to IRB-approved protocols
  • Supporting the informed consent process of research subjects
  • Coodinating protocol-related research procedures, study visits, and follow-up care
Qualifications:
  • Equivalent education and experience - High School Diploma and 1 year's relevant work experience in clinical research
  • At least 1 year experience working in a clinical research setting preferred
  • Working knowledge of clinical trials and Good Clinical Practices (GCP)
  • In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules
  • Ability to pay close attention to detail and establish effective working relationships
Estimated Salary Range:

$25.00-$39.00 per hour, dependent on qualifications and experience.



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