Job Description
Join NeuroVance Therapeutics at the forefront of neuroscience innovation! We're seeking a Clinical Research Associate to drive our groundbreaking Phase II trials for neurodegenerative therapeutics. As a key member of our clinical operations team, you'll ensure regulatory compliance while advancing treatments that impact millions. Enjoy competitive benefits, flexible work arrangements, and opportunities to present findings at international conferences.
Responsibilities
- Monitor clinical trial sites for protocol adherence and data integrity
- Conduct site visits, audits, and vendor management
- Ensure compliance with FDA regulations and ICH-GCP guidelines
- Manage clinical trial documentation and regulatory submissions
- Collaborate with cross-functional teams on trial design and execution
- Analyze safety data and prepare regulatory reports
Qualifications
- Bachelor's degree in life sciences, nursing, or related field
- Certified Clinical Research Associate (CCRA) required
- 3+ years of clinical monitoring experience in CNS trials
- Proficiency in EDC systems (Medidata Rave preferred)
- Strong knowledge of 21 CFR Part 11 and ICH-GCP
- Exceptional communication and problem-solving skills
- Ability to travel 25-30% domestically