Employer Industry: Healthcare Innovation and Medical Technology

Why consider this job opportunity:
- Salary up to $197,800
- Eligible for an annual performance bonus based on individual and corporate performance
- Comprehensive employee benefits including medical, dental, vision, and life insurance
- Opportunities for career advancement and participation in long-term incentive programs
- Flexible work arrangement with a fully remote position
- Generous time-off benefits, including vacation, sick time, and holidays

What to Expect (Job Responsibilities):
- Manage day-to-day operations of global clinical studies, ensuring compliance with clinical and regulatory standards
- Oversee project management activities, including vendor oversight and team communication
- Develop and maintain clinical trial documentation, including protocols and case report forms
- Conduct site visits to ensure protocol compliance and data accuracy
- Analyze clinical data and manage budgets, payments, and vendor performance throughout the study

What is Required (Qualifications):
- Bachelor's Degree in a scientific field, with consideration for other degrees
- Minimum of 10 years of experience in clinical research or related medical/scientific fields
- At least 1 year of experience managing clinical trials and projects; 2-3 years preferred
- Thorough knowledge of Good Clinical Practice (GCP) and applicable regulations
- Excellent verbal and written communication skills, with high attention to detail

How to Stand Out (Preferred Qualifications):
- Medical device experience strongly preferred
- Basic understanding of peripheral and coronary artery disease and therapies
- ACRP or SOCRA clinical research certification preferred
- Experience with EDC Data Management Systems
- Ability to manage multiple project teams in a fast-paced environment

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