Senior/Clinical Research Associate

"At Mobius, we only hire the best of the best. Our people are the primary reason for our success and the first pillar of our core values. As a leading CRO managing clinical trials across the USA, Australia, and New Zealand, we support a diverse portfolio of global and local clients across all phases of development and an array of therapeutic goods. We are committed to supporting our partners through every step of the clinical project journey, from rapid start-ups and comprehensive monitoring to precise data management, in-house EDC, and expedited study close-out." Job Description As a Senior Clinical Research Associate at Mobius, you will be the primary site manager, monitoring a variety of studies. This full-time position offers plenty of variety and the chance to make a significant impact as we strive to bring new therapies to those who need them. Minimum Requirements Bachelor's degree in life sciences or related field, # of years of related CV device experience, and/or clinicians who've moved into a CR position. 3+ years of CRA experience in med device, pharma, and/or biotech. Understands the clinical trial life cycle (FDA, IDE study, IRB, TMF, GCP, managed sites/audit/monitor). A utility player, team player who is self-empowered, challenges the team/asks questions, is comfortable wearing multiple hats, and possesses strong communication skills. Utilize IT, external, and study-specific software and tools. Comfortable with travel (1-2/week, depending on project). Job Requirements Oversee all aspects of clinical trial support from planning and start-up through monitoring and close-out. Collaborate with the VP and Manager of ClinOps to establish your project portfolio, monitoring schedules, and range of responsibilities. Ensure projects are executed in accordance with Mobius SOPs, study plans, and applicable regulations. Build and maintain strong relationships with investigators and their teams. Identify new opportunities to help and support site staff produce high-quality data and unparalleled compliance. Assist with budgeting, timekeeping, and billing. Troubleshoot and find compliant solutions to clinical trial issues. Hold regular project meetings and manage status reporting to Sponsors. Continuously enhance your knowledge of the clinical trials industry through training and professional development. Mentor colleagues with your expertise and practical solutions.

Location Territory Parameters:

Remote- will work on US-based projects.

Acceptable Candidate Location:

Remote- open to candidates residing in the Midwest, West, and Northeast.