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).