Senior Clinical Research Associate
Core
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
Role type
Senior Clinical Research Associate (Monitoring)
Builds
Clinical research studies in Phase II and III
Domain
Life Sciences / Clinical Research / Oncology
Deliverable
client delivery
Required skills
Independent on-site monitoring, compliance monitoring, site identification, feasibility research, regulatory document procurement, investigator training, automated tracking system maintenance, audit preparation and resolution
Preferred skills
Oncology study support experience
Technologies
MS Office applications
Responsibilities
Preparation, conduct, and reporting of monitoring visits; quality control and compliance monitoring; contact with clinical investigators, vendors, and support services; handling and reconciliation of Investigational Product(s) and trial supplies; training of investigators and site staff; involvement in site identification and feasibility research; support to Regulatory Affairs; delivering presentations at Investigator's Meetings; maintaining study-specific automated tracking systems; preparing for and attending company audits. (via careerplan.io/jobs/744000131127005-senior-clinical-research-associate-at-psi-cro)
Seniority
Mid-level, hands-on IC