![Grace Larsen](/sites/g/files/zrelqx296/files/styles/portrait_tablet/public/media/images/2023/Gracie%20Larsen.jpg?h=a0c2b571&itok=XoCeu4fD)
- Screen potential study participants
- Performs informed consent of participants.
- Completes, audits, and corrects CRFs.
- Reviews and ensures adherence to study protocol.
- Maintain complete records of research study activities.
- Transmission of clinical case data to the data management centers.
- Reviews and responds to case report form queries.