Clinical Trials Support Assistant

Jcct

Kansas City, Northern (KS, KY)

Hybrid

USD 35,000 - 52,000

Full time

10 days ago
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Job summary

JCCT is seeking a Research Assistant in its Clinical Operations department to support trial activities, ensure GCP/SOP compliance, and assist study coordinators. The role includes document preparation, data entry, subject recruitment, and protocol-specific tasks under supervision of the Site Manager.

The ideal candidate will have a high school diploma or GED (Bachelor’s preferred), experience in clinical research, and familiarity with clinical trial systems.

Qualifications

  • Required: High school diploma or GED; experience in clinical research preferred.
  • Preferred: Bachelor's degree and Medical Assistant certification.
  • Experience in medical history, medication history, and vital signs preferred.
  • Familiarity with clinical trial management systems is a plus.

Responsibilities

  • Maintain confidentiality of volunteers and sponsor information.
  • Provide administrative and operational support for clinical trials.
  • Prepare and manage study documents; data entry and query resolution.
  • Assist with screening, enrollment, and subject recruitment.
  • Support protocol-specific activities including vital signs and sample collection.
  • Track visits and communicate updates to study coordinators/PI.

Skills

Excellent communication
Bilingual Spanish/English
Organizational skills
Attention to detail
Microsoft Office
Medical terminology
Independent worker

Education

High School diploma or GED
Bachelor’s degree preferred
Experience in clinical research
Medical Assistant certification preferred
Experience with medical history and vital signs

Tools

Medidata Rave
Inform
TrialKit

Job description

JCCT is seeking a Research Assistant in its Clinical Operations department to support trial activities, ensure GCP/SOP compliance, and assist study coordinators. The role includes document preparation, data entry, subject recruitment, and protocol-specific tasks under supervision of the Site Manager.

The ideal candidate will have a high school diploma or GED (Bachelor’s preferred), experience in clinical research, and familiarity with clinical trial systems.

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