We are in need of someone who has an interest and/or experience in clinical research and can work with our researchers to perform studies. The successful candidate will assist researchers with entering patient data, document review, and other administrative duties as necessary. This person will also be responsible for creating studies, developing protocols, and managing study tasks.
Responsibilities:
- Assist with the recruitment and retention of study participants.
- Conduct telephone screening and in-person interview of potential study participants.
- Detailed understanding of the research protocol to ensure study conduct with scientific integrity.
- Demonstrate effective interpersonal skills to build rapport with potential study participants.
- Provide timely availability of clear and concise information to study coordinators and principal investigators.
- Participate in educational meetings with study staff to enhance knowledge on the research protocol.
- Exhibit thorough understanding of procedures and rules related to electronic data capture systems.
Job Type: Full-time
Pay: $18.00 - $27.00 per hour
Expected hours: 30 – 40 per week
Benefits:
- Flexible schedule
- Health insurance
- Paid time off
Experience level:
Medical specialties:
Schedule:
Work Location: In person