Apr 28, 2022
South Korea

Job Description

The CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Phase I-IV Oncology and Pharma clinical trials within the country.
The CRA is responsible to deliver data within timelines and required quality standard, responsible for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

Degree in scientific or healthcare discipline.
Fluent English (Oral and spoken), Fluent in local language

• Up to 2 years pharmaceutical industry experience or other relevant experience
• Good knowledge of drug development process specifically clinical trial/research
• Knowledge of international standards (GCP/ICH, FDA, EMEA)
• Monitoring experience is desirable
• Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.
• A minimum of 50% overnight travel may be required.
• Good communication skills, ability to influence others.
• Excellent communicator and presenter (oral and written), ability to communicate to Sr. Leaders
• Ability to manage sites independently; Proven ability to work independently with minimal supervision
• Good strategic thinking:
• Ability to anticipate potential issues and take appropriate actions with or without supervision.
• Advanced data accuracy: Ability to work focused with a great attention to detail
Global Drug Development
South Korea
Research & Development
Full Time
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Clinical Research Associate (CRA)

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