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Clinical Trials Coordinator
2 months ago
This part-time role involves supporting clinical research initiatives at The Lundquist Institute. The ideal candidate will have a strong foundation in medical sciences and a passion for advancing healthcare through research.
Essential Qualifications:
- Preferred: Bachelor's Degree, particularly for those interested in a medical career.
- Bilingual proficiency in English and Spanish is required.
Key Responsibilities:
- Oversee the management of clinical trials, ensuring effective communication with participants.
- Ensure adherence to clinical trial protocols and regulatory compliance.
- Plan and coordinate meetings and appointments related to research activities.
- Manage the entire lifecycle of clinical research studies, from initiation to completion.
- Maintain compliance with all relevant regulations and guidelines.
- Handle study documentation, including informed consent and protocol management.
- Accurately collect and record data in a timely manner.
- Perform phlebotomy tasks as required (training will be provided upon hiring).
- Review documentation for accuracy and completeness.
- Monitor participant progress throughout the study duration.
- Uphold high standards of quality control and data integrity.
- Adhere to Good Clinical Practice (GCP) standards.
Compensation:
$24 per hour.