Clinical Laboratory Scientist

SPECIFIC DUTIES/TASKS THE CONTRACT EMPLOYEE SHALL:

• 1. Evaluates protocols for compliance with applicable regulations governing human subjects protection.
• 2. If approved by the COR or KO contractor employees may be authorized to work a schedule that differs from the Anticipated Duty Hours.
• 3. Contractor is required to follow mandatory documents to the extent they apply to this contract. Any such changes to mandatory publications which cause a change in the scope of performance within the meaning of the Changes clause will not be implemented by the Contractor until a change in order or modification is issued by the KO.
• 4. Provides oversight and coordinates the functions associated with an honest broker system.
• 5. Analyzes the role and impact of other auxiliary departments on the proposed studies and coordinates their input.
• 6. Participates with the Principal Investigator in the scientific design of protocols associated with studies and makes recommendations on methodology.
• 7. Assures the proper documentation of project/study giving particular attention to any protocol modifications.

1. Requires a BS RN or BSN degree or equivalent and 2-5 years of experience in the field or in a related area.
2. Professional knowledge of a wide range of scientific and biomedical concepts principles and practices to perform the highly specialized tasks of developing and supporting proposed and active clinical cases; interpreting regulations associated with the studies and identifying potential threats to compliance with regulations and requirements in clinical settings; and ability to communicate with physicians and other healthcare personnel in a professional capacity.
3. Working knowledge of a significant body of scientific biomedical concepts and terminology and medical concepts and terminology.