RFI form
Please submit your RFI/RFP here. Our team will revert at the earliest.
Grow your career with one of the most flexible & result-oriented CROs in the industry
CRA must have a minimum of 2 years of on-site monitoring experience.
1. BASIC FUNCTIONS:
Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting pre-study, initiation, interim and close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by CliniRx and sponsors. Works closely with the Clinical Trial / Project Manager to ensure all monitoring activities are conducted according to study requirements.
2. ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:
3. KNOWLEDGE, SKILLS AND ABILITIES:
4. CRITICAL JOB FUNCTIONS IN ACCORDANCE WITH CRITERIA:
5. MINIMUM RECRUITMENT STANDARDS:
Please submit your RFI/RFP here. Our team will revert at the earliest.