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).
Clinical Study Coordinator
Clincial Study Coordinator for a fulltime, contract-to-hire position with a research site in Phoenix, AZ. The Study Coordinator 1 has the following duties:. Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures, and operating systems i...
Clinical Study Coordinator
A0;is seeking a Clincial Study Coordinator for a fulltime, contract-to-hire position with a research site in Phoenix, AZ. The Study Coordinator 1 has the following duties: . Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures, an...
Clinical Study Coordinator
A0;is seeking a Clincial Study Coordinator for a fulltime, contract-to-hire position with a research site in Phoenix, AZ. The Study Coordinator 1 has the following duties: . Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures, an...
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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. Oversees the planning, scheduling, and execution of daily clinical activities, optimizin...
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