Research Operations Manager
7 days ago
**Job Overview:**
Fortrea is seeking a highly skilled Clinical Research Associate II to join our team. The successful candidate will be responsible for conducting site monitoring responsibilities for clinical trials, ensuring data integrity, and maintaining quality control.
Key Responsibilities:
- Study Management:
- Manage study activities and ensure compliance with protocol procedures.
- Data Review:
- Review source documents carefully and verify accuracy against established data review guidelines.
- Travel and Training:
- Prepare and submit accurate and timely trip reports.
- Attend investigators' meetings and project team meetings as required.
**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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