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A Senior Clinical Research Associate is sought by Fortrea, a leading global contract research organization. The successful candidate will be responsible for conducting site monitoring responsibilities for clinical trials according to Fortrea's Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.
Key Responsibilities- Ensures the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study.
- Monitors data for missing or implausible data, ensuring study data completeness, accuracy, consistency, and compliance.
- Tracks IP shipments and supplies, as needed.
- Works closely with the study team, aligning monitoring to critical study timelines ensuring study deliverables are met.
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution.
- A minimum of 2 years of Clinical Monitoring experience.
- Fluent in local office language and in English, both written and verbal.
$80,000 - $110,000 per annum, depending on experience.
About FortreaFortrea is a 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.
