CareerPlan
Beijing - CNFull-time2026-10-08 → 2026-11-10

Core

Primary point of contact at the clinical trial site level responsible for study startup and overseeing quality, integrity, and compliance of clinical trial sites.

Role type

Clinical Research Associate (CRA)

Builds

Clinical trial sites

Domain

Healthcare / Clinical Research

Deliverable

client delivery

Required skills

Study startup, site monitoring, protocol adherence, GCP compliance, regulatory requirements knowledge, SOP adherence

Responsibilities

Study startup at site, oversee quality and integrity of clinical trial sites, ensure compliance with protocol, SOPs, ICH GCP, and regulatory requirements