AbbVie

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Clinical Research Associate II

Added

21 days ago

Location

🇨🇳 Beijing

Type

Full time

Salary

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Related skills

gcp monitoring clinical research ich guidelines site management

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📋 Description

Primary Sponsor point of contact for investigative sites
Aligns, trains and motivates site staff on trial goals
Conducts site evaluation, training, routine monitoring, and closure
Customizes site engagement strategies and tracks progress
Connects protocol and scientific principles to trial execution
Mentors and trains less experienced CRAs

🎯 Requirements

Tertiary qualification in health-related disciplines preferred
Minimum 3 years clinical experience, 2 in independent monitoring
Knowledge of therapeutic area and clinical trial conduct
Familiar with regulations, ICH/GCP guidelines
Advanced communication and cross-functional collaboration
Superior planning, organizational, and critical thinking skills

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