Clinical Monitoring Lead
7 days ago
**Job Description:**
We are seeking an experienced Clinical Research Associate II to conduct site monitoring responsibilities for clinical trials. The ideal candidate will have excellent communication skills and be able to work effectively in a matrix environment.
Key Responsibilities:
- Study Coordination:
- Coordinate study activities with study staff and ensure compliance with protocol procedures.
- Query Generation and Resolution:
- Generate and resolve queries as necessary.
- Travel and Reporting:
- Prepare and submit accurate and timely trip reports.
**Requirements:**
- Qualifications:
- University or college degree, or certification in a related allied health profession.
- Thorough understanding of ICH GCP Guidelines and local regulatory requirements.
- Basic understanding of the clinical trial process.
- Fluent in English, both written and verbal.
Experience:
A minimum of 2 years of Clinical Monitoring experience.Ability to work with minimal supervision.-
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