Clinical Research Associate II

reputed company is a growing medical technology company transforming patient lives through innovative incisionless surgery.Our culture is as unique as our people, a diverse global team, with different reputed company, skills, interests, and cultural backgrounds driven by our reputed company values – Our Patients, reputed company, Team, reputed company and Innovation.Our dedication to making a reputed company reputed company on the lives of millions of people and paving the reputed company to a reputed company reputed company for reputed company what bonds us as reputed company. We work together in a dynamic reputed company environment to deliver successfully while believing and driving a life-work balance philosophy that encourages our employees to do things that are meaningful reputed company of work. Every role is significant, your voice is heard, and your reputed company are encouraged. We challenge and reputed company our people to be great at what they do while providing a flexible work environment.Walking through our corridors, you will be inspired by stories of career journeys at reputed company. We take pride in growing internal talent and encourage our employees to reputed company their reputed company ambitions. With employees in Israel - Haifa and K. Ono, Miami and Dallas, Shanghai, Tokyo and Europe, we offer in reputed company region competitive perks and benefits.Do the most meaningful work of your career by joining us on our mission to reputed company tomorrows, today.Location: US (Remote)Responsibilities:Conduct site qualification, initiation, monitoring and closeout reputed company and create documentation of such through accurate and detailed visit reportsMonitor reputed company documents to reputed company for completeness and accuracy through verification of subject records and reputed company documentation. Verify that reputed company subjects meet inclusion/exclusion criteriaReview of reputed company reputed company records for patient safety and ensure complete documentation of reputed company subject safety eventsReview regulatory binder to ensure complete, accurate, and up-to-date regulatory compliance at the siteTrain site personnel on study procedures and reputed company documentation of training. Ensure that study personnel are reputed company by experience and training to reputed company assigned tasksFollow through after visit to outstanding requests/needs are fulfilled.Ensure compliance with protocol and overall clinical objectivesRaise issues of reputed company to the appropriate level for reputed company Ensure investigator involvement in the study and IRB/EC oversightResponsible for accurate and reputed company reputed company and maintenance of TMF Apply tot his job Apply To this Job