Clinical Research Coordinator, Administration, Full Time, Day Shift

Position Summary:                        

The Clinical Research Coordinator (CRC) will assist the Principal Investigator in the conduct all aspects of the clinical trial, including regulatory tasks, under the direct supervision of the CARE Clinical Research Director.

The CRC provides operational and administrative support in the management of patients accrued to multiple research protocols to assure subjects’ safety and regulatory compliance.

The CRC is responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, Standard Operating Procedures and all applicable regulations and guidelines and ensuring effective data flow associated with research protocols.                       

Position Qualification: (Training, Education, Experience, Skills and Abilities):                       

• AS Degree in Science, Healthcare, or a related field and 2 years of experience as a Clinical Research Coordinator.
• Applicant must be willing to obtain a research related certification within a year of employment.
• Knowledge of medical terminology. Ability to manage multiple tasks simultaneously. Attention to detail & accuracy.                  

Required Licenses/Certifications:  

• Applicant must be willing to obtain a research related certification within a year of employment.                   

Communication Skills:                     

• Ability to effectively communicate in writing and orally with all levels of the organization