Clinical Research Coordinator
4 weeks ago
We are seeking a highly organized and detail-oriented Clinical Research Assistant to join our team at Bayview Research Group. The successful candidate will be responsible for scheduling study participant visits, completing study procedures, and maintaining accurate source documents.
Key Responsibilities:
- Schedule study participant visits and complete study procedures, including phlebotomy, sample processing, and vital signs.
- Ensure accurate and timely data collection, documentation, entry, and reporting.
- Maintain accurate source documents related to all research procedures.
- Responsible for all filings, including reports and source documents.
- Maintain research practices using Good Clinical Practice (GCP) Guidelines.
- Maintain strict patient confidentiality according to HIPAA regulations and applicable law.
- Participate in required training and education programs.
- Ensure all study communication is consistently documented and communicated to appropriate team members.
Requirements:
- High school diploma or equivalent required; associate's degree or higher preferred.
- Knowledge of medical terminology and human anatomy.
- High level of computer literacy using Microsoft Windows, Word, Excel, and Outlook.
- Active Phlebotomy License CPT-I required.
- English fluency is a must.
- Excellent bedside manner when dealing with study participants.
- Ability to work in a fast-paced environment and prioritize tasks effectively.
Benefits:
- Dental insurance.
- Health insurance.
- Paid time off.
Work Environment:
- Clinic.
- In-person.
- Office.
- Private practice.
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