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　　Site Monitor - all US locations United States of America, Remote Additional Locations: Remote - United States of America Job IDR0000019739 CategoryClinical Trials

　　Apply Now (https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/United-States-North-Carolina-Remote/Site-Monitor---all-US-locations_R0000019739) Save Job

　　About 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)

　　Skills and 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

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　　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.