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hace 2 meses
We are seeking a highly skilled Clinical Research Associate to join our team at CDS Fortrea Inc. As a Clinical Research Associate, you will be responsible for monitoring clinical sites, maintaining study files, and conducting pre-study and initiation visits. You will also be responsible for ensuring the integrity of data submitted on Case Report Forms (CRFs) and monitoring data for missing or implausible data.
Key Responsibilities- Monitor study sites to ensure compliance with protocol and regulatory requirements
- Maintain study files and ensure accurate and timely data submission
- Conduct pre-study and initiation visits to ensure study staff are properly trained
- Verify informed consent procedures and protocol requirements are adhered to
- Monitor data for missing or implausible data and ensure audit readiness
- Prepare accurate and timely trip reports
- University or college degree, or certification in a related allied health profession
- Thorough knowledge of ICH Guidelines and local regulatory requirements
- Strong experience with Clinical Monitoring
- Ability to monitor study sites independently and work with minimal supervision
- Good communication and interpersonal skills
- Computer competency and fluency in English
CDS Fortrea Inc. is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. We are committed to revolutionizing the development process and ensuring the swift delivery of life-changing ideas and therapies to patients in need.
