Senior Clinical Research Associate/ Clinical Research Associate II
Core
Monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and regulations.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and regulatory compliance for oncology and rare disease studies
Domain
Clinical research / Oncology
Required skills
Site monitoring, regulatory compliance (ICH-GCP), risk identification, conflict resolution, study setup coordination, protocol adherence
Preferred skills
Oncology experience, early phase experience (via careerplan.io/jobs/5748061004-senior-clinical-research-associate-clinical-research-associate-ii-at-precisionmedicinegrou)
Technologies
ICH-GCP, SOPs
Responsibilities
Conduct pre-study and initiation visits, coordinate regulatory submissions, monitor study progress at sites, identify and mitigate study risks, prepare for investigator meetings
Seniority
Senior, hands-on IC