تم وضع المناقشة في: غيرها في لاس فيجاس | علق: |
Job Description
The Clinical Research Coordinator (CRC)/Rater is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC manages, supports, facilitates and coordinates the daily clinical trial activities, performs psychometric rating scales, and plays a critical role in the conduct of the study.
Essential Duties and Responsibilities:
Assisting trial Investigator in screening and review of potential study participants eligibility
Administering semi-structured test or rater scales as per protocol, not limited to CDR, ADAS-COG, MMSE, CSSRS, Cognitive Battery Test, ESS, and like exams
Complete provided rater training and Good Clinical Practice (GCP) training
Conduct interviews following specific study protocols, FDA, GCP, ICH, and HIPAA Privacy guidelines
Maintaining case report forms, charts and documentation
Mentoring, training, and high-level oversight of other clinical research coordinators and research assistants
Ensuring that all clinical activities are carried out in accordance with established research protocol and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
Collecting and entering data as necessary
Assist management with potential new hire selection and shadowing process.
Assist with study start-up, maintenance, and close-out of studies as needed for those on the team
Ability to be flexible with study assignments