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Research Study Associate
2 months ago
Position: Research Study Associate
The Research Study Associate plays a crucial role in supporting clinical research activities by facilitating patient interactions in accordance with established guidelines and protocols. The responsibilities may vary based on individual expertise and the evolving needs of the organization.
Key Responsibilities
- Manage and organize patient appointments in alignment with study-specific timelines.
- Prepare necessary documentation and records for the Clinical Research Coordinator.
- Observe and assist the Coordinator in patient care and management.
- Support the Coordinator in monitoring patient flow and ensuring proper care.
- Collect and document essential data during follow-up visits, including adverse events and concurrent medications.
- Transfer patient study information from original documents to Electronic Case Report Forms.
- Administer required questionnaires to study participants.
- Set up and conduct electrocardiograms (ECG) as dictated by the study protocol.
- Request and manage medical records for Serious Adverse Event Reporting.
- Handle and ship biological samples for laboratory analysis.
- Conduct intraocular pressure assessments post-injection.
- Perform visual acuity testing and trial frame refraction as needed.
- Inform participants and secure written re-consents regarding informed consent forms.
- Execute additional tasks as assigned.
- Complete any necessary sponsor training and certifications.