Senior Clinical Research Associate
Core
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications, focusing on subjects' rights, safety, well-being, and data quality compliance.
Role type
Senior Clinical Research Associate (CRA) (via careerplan.io/jobs/744000152633691-senior-clinical-research-associate-at-psi-cro)
Builds
Clinical research studies in Phase II and/or III
Domain
Clinical Research / Life Sciences
Required skills
On-site monitoring, study startup, CRF review, source document verification, query resolution, site communication and management, schedule supervision, regulatory document preparation, feasibility research
Preferred skills
Oncology study experience, advanced MS Office knowledge
Technologies
MS Office
Responsibilities
Conducting and reporting onsite monitoring visits, driving study startup phase, performing CRF reviews and source document verification, managing site communication, supervising study activities and timelines, acting as point of contact for support services and vendors, supporting quality control and compliance monitoring, participating in feasibility research, supporting regulatory team in study submissions
Seniority
Senior, hands-on IC