In-House Clinical Research Associate, CRA

Job Description: • Support study execution by managing meeting logistics, documenting decisions, and tracking action items. • Partner with Clinical Operations and site monitors to ensure protocol compliance and quality standards are met. • Responsible for filing the site-level documents into the Trial Master Files (TMFs) in a timely manner. • Track, review, and organize essential documents from sites and vendors. • Identify, escalate, and help resolve site-level issues in collaboration with cross-functional teams. • Assist with regulatory submissions and other study deliverables. • Drive process improvements that enhance speed, quality, and patient impact. Requirements: • Bachelor’s degree in a life science or health-related field, or equivalent industry experience. • 5+ years of clinical trial experience in biotech, pharma, or CRO settings. • Solid knowledge of GCP, ICH guidelines, and regulatory requirements. • Exceptional organizational and communication skills. • A proactive, problem-solving mindset with high attention to detail. • Comfortable managing multiple priorities in a fast-paced, mission-driven environment. • Strong team player who thrives in flat, agile organizations. • Proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook). Benefits: • 99% of premium paid for medical, dental, and vision plans. • Company-paid life insurance, AD&D, and disability benefits. • Voluntary plans to personalize coverage. • 401(k) matching up to 6% on eligible contributions. • Long-term stock incentives and ESPP. • Discretionary quarterly bonus. • Flexible wellness benefit. • Generous PTO and paid holidays. • Company-wide shutdowns. Apply tot his job