
> Central Monitor, Oncology
2 semanas atrás
Clinical Research Associate (CRA) Job Description
">Our organization is seeking a dedicated Clinical Research Associate (CRA) to play a key role in the successful execution of clinical trials. The CRA will be responsible for conducting all types of site visits, collaborating with site staff, delivering protocol and study-specific training, assessing site performance, and ensuring compliance and data integrity.
">Required Skills and Qualifications
">- ">
- A Bachelor's degree in life sciences or a health-related field (or equivalent experience).">
- At least 1 year of on-site monitoring experience.">
- A strong understanding of GCP, ICH guidelines, and regulatory requirements.">
- The ability to travel as required by the project.">
Benefits
">This is an excellent opportunity for a motivated and detail-oriented individual to join our team and contribute to the success of our clinical trials.
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