Job Description

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

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