Senior Clinical Research Associate - 998

***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