CRA II
On-siteTaipei, Taiwan, Taiwan
EXPIREDTaipei, Taiwan, TaiwanOn-siteFull TimeBachelors DegreeEnterprise
Full TimeBachelors DegreeEnterprise
Job Summary
Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance, data integrity, and patient safety. Collaborate with investigators and site staff to facilitate smooth study conduct, perform data review and query resolution, and contribute to the preparation of study documentation including protocols and clinical study reports. Requires a Bachelor's degree, minimum 2 years CRA experience, and ability to travel 60% of the time with a valid driver's license. Based in ICON Taipei office with flex schedule.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Minimum of 2 years of experience as a Clinical Research Associate
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment
- Ability to travel at least 60% of the time (international and domestic - fly and drive)
- Valid driver's license
- Legal right to work in the country where the role is based
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