Clinical Research Associate II
Core
Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, ICH-GCP, and regulations.
Role type
Clinical Research Associate II
Builds
Clinical trial execution for life sciences therapies
Domain
Life Sciences / Oncology / Rare Disease
Required skills
Clinical study monitoring, Site management, Regulatory compliance (ICH-GCP), Risk identification, Protocol adherence, Investigator coordination
Preferred skills
Study start-up activities, Oncology monitoring experience
Technologies
Clinical trial management systems, Regulatory databases
Responsibilities
Conduct pre-study and initiation visits, Coordinate regulatory submissions, Ensure data recording and reporting per protocol, Identify and mitigate study risks, Manage investigator relationships (via careerplan.io/jobs/6121350004-clinical-research-associate-ii-at-precisionmedicinegroup)
Seniority
Mid-level, hands-on IC