Clinical Research Associate II/ Senior Clinical Research Associate
No visa sponsorship
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 (Oncology)
Builds
Clinical trial data and regulatory submissions for oncology therapies
Domain
Biopharmaceuticals / Oncology
Deliverable
physical/clinical work
Required skills
Site monitoring, protocol adherence, risk identification, regulatory compliance, conflict resolution, investigator coordination
Preferred skills
Oncology experience, Phase I experience, First-In-Human (FIH) experience
Technologies
ICH-GCP, SOPs
Responsibilities
Conduct pre-study and initiation visits, coordinate study setup activities, identify investigators, mitigate study risks, ensure data quality and regulatory compliance
Seniority
Senior, hands-on IC
