Bachelor's degree in a life sciences-related field, Registered Nursing certification, or an equivalent and relevant formal academic or vocational qualification.
Previous experience as a clinical research monitor, typically comparable to at least 2+ years of independent clinical monitoring experience.
Valid driver's license where applicable to support required travel.
Effective clinical monitoring skills, including experience with on-site and remote monitoring activities.
Demonstrated understanding of medical and therapeutic area concepts and medical terminology.
Excellent understanding and practical application of ICH-GCP guidelines, applicable regulations, and procedural documents.
Ability to manage and apply Risk Based Monitoring concepts and processes in daily monitoring activities.
Good computer skills, including proficient use of Microsoft Office applications and the ability to learn and use clinical trial software and systems such as CTMS.
Good command of the English language, including strong grammar and business writing skills.
Willingness to travel extensively to support on-site monitoring activities.
100% home-based within the United States