Global Clinical Monitor
hace 1 semana
We are seeking a highly motivated and experienced Global Clinical Monitor to join our team at CDS Fortrea Inc. This is an exciting opportunity to work on clinical trials, driving drug development forward.
Job SummaryThe Global Clinical Monitor will be responsible for monitoring study sites independently, ensuring compliance with protocol monitoring guidelines, SOPs, and local regulatory requirements. This includes conducting pre-study and initiation visits, maintaining study files, and liaising with vendors.
Main Responsibilities- Monitor study sites independently, adhering to protocol monitoring guidelines, SOPs, and local regulatory requirements.
- Conduct pre-study and initiation visits, maintain study files, and liaise with vendors.
- Ensure informed consent procedures and protocol requirements are met according to applicable regulatory requirements.
- Verify data accuracy on Case Report Forms (CRFs) or other data collection tools through source document review.
- Monitor data for missing or implausible information.
- Ensure efficient use of Sponsor and Labcorp resources by performing monitoring tasks according to SOPs and established guidelines.
- Prepare accurate and timely trip reports.
- University or college degree in a related field or certification in a related allied health profession from an accredited institution.
- Thorough knowledge of ICH Guidelines and understanding of local regulatory requirements.
- Strong experience in clinical monitoring.
- Ability to work with minimal supervision.
- Good communication and interpersonal skills.
- Computer competency.
- Fluent in English, both written and verbal.
$85,000 - $115,000 per year, depending on location and experience.
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