Clinical Research Assistant
$39,520–$68,640 year
On-siteMauldin, South Carolina, United States
Job Summary
Conduct patient coordination by obtaining informed consent, scheduling visits, collecting and shipping specimens, and performing basic clinical procedures like blood draws and vital signs under CRC direction. Execute documentation duties including recording data in real time, updating trackers, assisting with recruitment phone screenings, and resolving queries. Manage administrative tasks such as maintaining site logs, ordering supplies, and interacting professionally with participants and investigators. Maintain adherence to FDA regulations, ICH guidelines, and Good Clinical Practices while working independently in a fast-paced environment. Requires bilingual Spanish proficiency, phlebotomy experience, and a minimum of one year in a clinical role.
Required Qualifications
- Bilingual in Spanish
- Ability and willingness to work independently with minimal supervision
- Ability to learn to work in a fast-paced environment
- Excellent communication skills
- High degree of professionalism
- Excellent organizational skills
- Strong attention to detail
- A working knowledge of medical and research terminology
- A working knowledge of federal regulations, Good Clinical Practices (GCP)
- Critical thinker and problem solver
- Ability to maintain a positive attitude under pressure
- Proficiency in Microsoft Office Suite
- High level of self-motivation and energy
- An optimistic, 'can do' attitude
- Phlebotomy Experience and Proficiency
- A minimum of 1-year recent working experience as a Medical Assistant, EMT, LPN, Clinical Research Assistant or Phlebotomist
- Regularly planned travel within the region
- Overnight travel (<10%)
Desired Qualifications
- Some Clinical Research experience
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