Clinical Trials Coordinator
2 weeks ago
The Lundquist Institute is seeking a dedicated professional to assist in the management of clinical research studies. This part-time role involves various responsibilities aimed at ensuring the smooth operation of clinical trials.
Essential Qualifications:
- A Bachelor's Degree is preferred, particularly for those interested in a medical career.
- Bilingual proficiency in English and Spanish is required.
Key Responsibilities:
- Oversee the management of clinical trials, including patient interactions and document handling.
- Ensure compliance with clinical trial protocols while managing participant involvement.
- Facilitate communication, planning, and scheduling of necessary meetings and appointments.
- Coordinate and supervise clinical research projects from initiation to completion.
- Maintain adherence to all relevant regulations and guidelines.
- Manage study-related documentation, including informed consent forms and research protocols.
- Accurately collect and record data in a timely manner.
- Perform phlebotomy as required (training will be provided upon hiring).
- Review and confirm the accuracy and completeness of documentation.
- Monitor participant progress throughout the study duration.
- Uphold high standards of quality control and data integrity.
- Follow Good Clinical Practice (GCP) guidelines diligently.
Compensation:
$24 per hour.
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