Clinical Research Associate II
Core
Manage clinical aspects of full-service global clinical research projects in Taiwan, ensuring timelines, standards, and subject safety. (via careerplan.io/jobs/744000153933395-clinical-research-associate-ii-at-psi-cro)
Role type
Clinical Research Associate II (IC)
Builds
Clinical trial data and regulatory submissions for pharmaceutical clients
Domain
Clinical Research / Life Sciences
Required skills
On-site monitoring, Source document verification, CRF review, Query resolution, Site management, Feasibility research, Contract negotiation, Regulatory document preparation
Preferred skills
Therapeutic area experience (Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases)
Technologies
Clinical trial management systems, Electronic data capture (implied via CRF review)
Responsibilities
Conduct onsite monitoring visits, Perform study startup activities, Monitor trial progress at country level, Facilitate site budgets and contract negotiations, Serve as point of contact for vendors and internal teams, Participate in feasibility research
Seniority
Mid-level, hands-on IC