Role OverviewWe are seeking a detail-oriented and proactive Sr. Clinical Trial Associate to support the successful execution of clinical studies within Clinical Operations. In this role, you will partner closely with study leads and cross-functional teams to manage key components of clinical trials, ensuring delivery against timelines, budgets, and quality standards.
What You Will Do
Coordinate cross-functional study team meetings, support clinical site start-up activities, manage external vendors, participate in Investigator Meetings, maintain and track study documentation, and support Trial Master File management.
Why It Might Be a Fit
This is an excellent opportunity for a clinical operations professional who thrives in a fast-paced environment and is eager to contribute to high-impact clinical programs.
Requirements
- Bachelor’s or Master’s degree
- At least 3 years of clinical operations experience in a pharmaceutical company and/or CRO
- Solid understanding of ICH guidelines, GCP, and key regulatory requirements
- Ability to independently manage assigned components of clinical trials with minimal oversight
- Strong attention to detail and organizational skills
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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