Regulatory Coordinator

📋 Description

• Manage the documentation submission process, ensuring timely initiation of new clinical research
• Support quality documentation and training processes for our clinical trials, delivering timely and
• Maintain site staff certifications and supporting documentation.
• Carefully researching and responding to client inquiries or requests for information related to our
• Deliver clear, consistent communication to our clinical research locations about forthcoming trial
• Assist with the initial setup of new clinical trial sites.

🎯 Requirements

• At least two years of administration or project management experience.
• Exceptional organizational skills with strong attention to detail.
• Advanced problem-solving skills and adaptability, the ability to follow tasks through to completion.
• Proficiency with Apple computers, Google Workspace applications, and management of other relevant
• Bachelor's degree from an accredited university OR 3 years of equivalent professional experience in
• A self-motivated, positive approach to work and collaboration.

🎁 Benefits

• Medical Insurance, with generous employer paid contributions
• Dental and Vision Insurance
• Short and Long Term Disability and Group Life Coverage
• Paid Time Off that builds throughout your career with the company
• 401K (+ discretionary match/profit sharing)
• Quarterly Bonus Plan that clearly outlines your bonus potential per quarter and gives the team the