Site Monitor/Clinical Research Associate - FSP
United States of America, Remote 求人ID R0000025624 Category Clinical TrialsAbout this Role
The Site Monitor will be responsible for data integrity, data quality and ensuring compliance with ICH GCP and local requirements at the site level.Monitoring will be conducted in line with the Study Monitoring Plan and will be performed virtually for the majority of activities to supplement on-site visit requirements.The Site Monitor will collaborate with the Site Manager to assure that the site is in compliance with the protocol and is inspection ready.
Education
- Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience
- Proficiency in local language preferred. English is required
Experience
- A minimum of 12 months experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite)
Skillsand Technical Competencies
- Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
- Must demonstrate good computer skills and be able to embrace new technologies
- Excellent communication, presentation and interpersonal skills
- Demonstrated networking and relationship building skills
- Ability to communicate effectively and appropriately with internal & external stakeholders
- Ability to adapt to changing technologies and processes
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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