Clinical Research Coordinator
2 hours ago
We are seeking a highly motivated and detail-oriented Clinical Research Assistant to join our team at Vitreo-Retinal Medical Group, Inc. This is an exciting opportunity to work in a fast-paced medical office and contribute to the advancement of retina care.
The successful candidate will be responsible for assisting in research patient visits, coordinating study protocols, and ensuring compliance with ICH-GCP guidelines and IRB-approved study protocols.
Key Responsibilities:
- Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
- Prepare visit-specific documentation and charts for Clinical Research Coordinator.
- Observe and assist in monitoring subject flow and subject care and management.
- Transcribe subject study information from source documents to the Electronic Case Report Forms.
- Administer all mandatory questionnaires to study subjects.
- Set up, prepare subject, and conduct electrocardiograms (ECG) on subjects as required per study protocol.
- Promptly request all necessary medical records for Serious Adverse Event Reporting.
- Process and ship laboratory biological samples for analysis.
- Perform intraocular pressure checks after injections.
- Perform trial frame refraction and visual acuity testing.
Requirements:
- High school diploma or equivalent required.
- 1-2 years of experience in clinical research or a related field preferred.
- Excellent communication and organizational skills.
- Ability to work independently and as part of a team.
What We Offer:
- A dynamic and supportive work environment.
- Opportunities for professional growth and development.
- A competitive salary and benefits package.
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