Clinical Research Associate II Position
3 weeks ago
Job Summary
As a Clinical Research Associate II at PSI, you will be responsible for conducting on-site monitoring visits, reviewing CRFs, and verifying source documents. Your primary goal will be to ensure the highest quality standards in the industry.
You will:
- Conduct and report onsite monitoring visits for SSV, SIV, RMV, and COV studies.
- Perform CRF review, source document verification, and query resolution.
- Manage site communication and collaborate with internal project teams.
- Participate in feasibility research and support regulatory teams.
Qualifications
To be successful in this role, you should have:
- A college or university degree in Life Sciences or a relevant field.
- At least 2-3 years of independent on-site monitoring experience in China.
- Experience with all types of monitoring visits in Phase II and/or III.
- Therapeutic area experience in Oncology is a plus.
- Full working proficiency in English and Mandarin.
About PSI
At PSI, we offer a dynamic work environment, extensive training, and a competitive salary package. You will have the opportunity to advance your career in clinical research and work closely with driven and dedicated cross-functional teams.
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