Senior Clinical Research Associate

This position can work remotely anywhere in the United States*** What's in it for YOU? Competitive compensation with comprehensive medical, vision, and dental benefits package Unlimited PTO package with additional sick days 8 hours of additional PTO to volunteer for a charity of your choice and up to $120 paid to your charity for your commitment Wellness reimbursement up to $50 per month for fitness and wellness memberships Tuition reimbursement up to $5,000 per year Visibility and recognition by Senior leadership for positive contributions to the business Opportunity to have a voice and be a part of a very close-knit team (advice, reliability, mentorship, partnership) And more! Responsibilities: Ensure clinical trials are conducted in compliance with protocol/amendment(s), with ICH GCP, SOPs and with applicable regulatory requirements in the assigned countries and sites Ensure subject safety and verify diligence in protecting the confidentiality and wellbeing of study subjects Verify adequacy, completeness, reliability, and quality of trial data collected at study sites Conduct site qualification , site initiation, interim monitoring and close out visits Develop and maintain site and investigator relationships to ensure clinical trials are managed efficiently Qualifications: Bachelor's degree preferred; a Registered Nurse (RN) may also be considered 3+ years of clinical monitoring experience The ability to perform travel up to an average of 80%, depending on project needs This role may be office and/or home-based/field-based however regular infrequent visits to a Company office will also be required. Current passport or identity card with a valid driving license required