Key Responsibilities:

Assist with the planning, implementation, and coordination of clinical research studies.
Recruit, screen, and enroll study participants based on study protocols.
Schedule and conduct study visits, follow-ups, and patient assessments.
Maintain accurate and up-to-date source documents, case report forms (CRFs), and study records.
Assist in obtaining informed consent from study participants in accordance with ethical guidelines.
Collect, process, and ship biological samples as required by the protocol.
Communicate with institutional review boards (IRBs), sponsors, and other stakeholders.
Ensure compliance with all applicable regulatory requirements and protocols.
Enter and manage data using electronic data capture systems (EDC).
Assist with the preparation of study-related documentation, including reports, SOPs, and training materials.
Support monitoring visits, audits, and inspections