MSG
ICON plc
Clinical Research Associate
Full-Time
Seoul, South Korea
Health & Biotech
Health & Biotech
20 June 2024
Description
- Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
- Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
- Balancing sponsor generated queries
- Taking responsibility for study cost efficiency
- Preparation and review of study documentation and feasibility studies for new proposals
- Potential to assist in training and mentoring fellow CRAs
Qualifications
- 12 months+ of monitoring experience in phase I-III trials as a CRA
- Oncology monitoring experience upreferred
- College degree in medicine, science, or equivalent
- Previous monitoring experience in medium-sized studies, including study start-up and close-out
- Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
- Excellent written and verbal communication
- Ability to work to tight deadlines
- Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
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