Role OverviewWe are seeking a motivated and detail-oriented Clinical Trial Associate to support the execution of clinical studies within our Clinical Operations team. In this role, you will contribute to key trial activities and ensure that study components are delivered on time, within scope, and in compliance with quality and regulatory standards.
What You Will Do
Coordinate cross-functional study team meetings, prepare agendas, capture meeting minutes, support site start-up activities, and ongoing study coordination efforts. Maintain and track essential study documentation, including regulatory documents, and support Trial Master File activities.
Why It Might Be a Fit
This role requires a strong organizational skills, attention to detail, and ability to manage assigned study activities with guidance from senior team members. The ideal candidate will have a working knowledge of ICH guidelines, GCP, and global clinical trial regulations.
Requirements
- Bachelor’s or Master’s degree
- 1–3 years of experience in a pharmaceutical, biotech, CRO, or academic research setting
- Working knowledge of ICH guidelines, GCP, and global clinical trial regulations
- Ability to manage assigned study activities with guidance from senior team members
- Strong organizational skills and attention to detail
Benefits
- Competitive salary
- Annual bonus
- Comprehensive benefits package including medical, dental, vision insurance, 401(k) retirement plan with company match
- Generous parental leave and family planning benefits
- Outstanding culture and opportunities for personal and professional growth
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