Responsible for project activities associated with monitoring functions of phase I through phase IV clinical research studies and Real World Evidence (RWE) studies
Serve as the main CTI contact for assigned study sites
Conduct site visits including pre-study, site initiation, interim monitoring, and close-out
Collect, review, and track essential/regulatory documents
Assist with study start-up activities, including feasibility, pre-study activities, and site selection
Participate in and complete all general and study-specific training as required
Conduct remote monitoring and complete the related activities in accordance with the study-specific Monitoring Plan
Manage ISF and TMF for all assigned study sites in accordance with SOPs or study-specific Monitoring Plans

At least 1 year of clinical trial monitoring experience or equivalent
Bachelor's Degree or higher in an allied health field such as nursing, pharmacy, or health/natural science
RN with an Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience
Previous experience in conducting clinical research studies in a hospital setting, a pharmaceutical company, or a CRO
Demonstrated successful performance in a CRA position with a minimum of 1 year of on-site monitoring experience preferred

Senior Clinical Research Associate

Key skills