Clinical Research Associate
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Job Summary
To support the successful delivery of clinical trials, the full-time Clinical Research Associate will manage site qualification, monitoring, and close-out visits while ensuring patient safety and data quality in a hybrid work environment.
Key Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits in accordance with study protocols and regulations
- Ensure subject safety, data integrity, and protocol compliance throughout the study lifecycle
- Build and maintain strong relationships with investigators, study coordinators, and site personnel
Required Qualifications
- Bachelor's degree in Life Sciences or a related field
- 3-4 years of Clinical Research Associate experience within the pharmaceutical, biotechnology, or CRO industry
- Solid understanding of ICH-GCP, clinical trial processes, and applicable regulations
- Demonstrated ability to work independently and take ownership of site activities and deliverables
- Oncology and/or Phase I clinical trial experience is preferred but not essential
Complete Job Description
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