Responsibilities :
- Participates in and coordinates the planning, development, and implementation of clinical protocols, logistical procedures, and operating systems as per the study sponsor and Principal Investigator's guidelines.
- Supervises, evaluates, and coordinates the activities of Clinical Research Assistants, ensuring all clinical activities adhere to Company SOPs and Good Clinical Practices guidelines.
- Oversees the planning, scheduling, and execution of daily clinical activities, optimizing study workflow and research subject availability.
- Collaborates closely with the Recruitment Department to ensure compliance with specific research subject entrance criteria before conducting the study.
- Monitors test subjects' responses to treatment and promptly communicates study data and results to investigators.
- Works with Clinical Management to generate protocols, interim reports, and final reports for Company sponsors.
- Orders and maintains laboratory supply inventory.
Requirements :
- High School diploma or equivalent
- Bachelors of Science or Arts degree in life sciences preferred.
- 1 - 2 years' experience in clinical industry experience (substitute for BS or BA).
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