Clinical Trials Operations Specialist
1 month ago
As a leading global contract research organization, Fortrea is seeking a highly skilled Clinical Trials Operations Specialist to support our pharmaceutical, biotechnology, and medical device customers.
Typical Accountabilities
- Schedule and manage clinical trials, ensuring compliance with regulatory requirements.
- Develop and implement efficient clinical trial workflows, reducing timelines and costs.
- Collaborate with cross-functional teams to resolve complex clinical trial issues.
- Provide training and support to study sites, ensuring seamless trial execution.
- Maintain accurate and compliant trial documentation, including study protocols, informed consent forms, and regulatory submissions.
- Stay up-to-date with evolving regulatory requirements, ensuring our customers' trials remain compliant.
Requirements
- Bachelor's degree in a relevant field, such as life sciences, clinical research, or a related field.
- At least 2 years of experience in clinical trials operations, regulatory compliance, or a related field.
- Knowledge of ICH guidelines, GCP, and local regulations.
- Excellent communication and project management skills.
- Fluent in English, both written and spoken.
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