As a Clinical Research Assistant, you will play a crucial role in supporting the execution of clinical research studies and trials. Working under the supervision of the Principal Investigator or Clinical Research Coordinator, you will contribute to the efficient and ethical conduct of research by performing various tasks related to data collection, participant recruitment, and study coordination. This position requires attention to detail, strong organizational skills, and a commitment to maintaining compliance with regulatory requirements.
Responsibilities:
Participant Recruitment and Informed Consent:
Data Collection and Management:
Clinical Trial Coordination:
Regulatory Compliance:
Communication and Collaboration:
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