Senior Clinical Research Associate

We are looking for a Senior Clinical Research Associate to join our team. The successful candidate will be responsible for monitoring and site management activities to ensure timelines and deliverables are met at assigned sites. The role involves building and maintaining strong relationships with clinical sites and investigators, assessing protocol and regulatory compliance, and ensuring high quality data.

Requirements

• Bachelor’s degree in life sciences, medicine, or similar discipline.
• Minimum of six (6) years of industry experience in clinical research or equivalent experience gained with a CRO, pharmaceutical or medical device company.
• Thorough knowledge of ICH/GCP Guidelines, ISO 14155, and FDA and EU MDR, including a basic understanding of regulatory requirements in other countries.
• Advanced site monitoring skills.
• Ability to work with minimum supervision, excellent task management skills and collaboration, including verbal and written communication.
• Ability to travel (5-10%) domestically and internationally on an as-needed basis with advance notice.
• Knowledge of MS Office and clinical trial management systems.
• Full working proficiency in English.

Benefits

• Paid time off
• Paid volunteer time
• Medical, Dental, Vision and Flexible Spending Account
• Health Savings Account with Company Funded Contributions
• 401k Retirement Plan with Company Match
• Parental Leave and Adoption Services
• Health and Wellness Programs and Events