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Clinical Research Associate I/ Clinical Research Associate II

RemoteFull-time2026-10-05 → 2026-10-08
HybridNo visa sponsorship

Core

Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, and regulations.

Builds

Clinical trial execution for oncology and rare disease therapies

Domain

Life Sciences / Clinical Research / Oncology

Required skills

Site monitoring, regulatory compliance (ICH-GCP), study setup coordination, risk identification, conflict resolution, detail orientation

Preferred skills

Study start-up activities experience

Technologies

Clinical trial management systems, regulatory databases

Responsibilities

Conduct pre-study and initiation visits, coordinate regulatory submissions, identify investigators, monitor study progress, mitigate study risks

Seniority

Junior to Mid-level