Senior Clinical Trial Manager Associate Clinical Operations

📋 Description

• Manage clinical study vendors, including central laboratories, RTSM/IRT, imaging, dosimetry, and
• Participate actively in vendor meetings, contribute to operational planning, develop and monitor
• Support CRO management, including reviewing clinical study protocols, informed consent forms, study
• Participate in CRO and Study Execution Team meetings and contribute to operational strategy
• Support site management activities such as site feasibility assessments, site selection and
• Track and maintain study documentation, ensuring Trial Master File completeness, accuracy, and

🎯 Requirements

• 2-3+ years of clinical operations experience within the biotech, pharmaceutical, CRO, or related
• Bachelor's degree in a scientific, healthcare, life sciences, or related field preferred.
• Experience managing or coordinating external clinical vendors, with an understanding of
• Familiarity with clinical trial execution, CRO collaboration, site start-up, and study
• Working knowledge of Good Clinical Practice (GCP), ICH guidelines, FDA requirements, and clinical
• Strong organizational skills, high attention to detail, and consistent focus on quality and timely

🎁 Benefits

• Fully remote position within the United States.
• Full-time employment with a base salary range of $119,116-$144,341, based on factors such as
• Eligibility for additional discretionary incentive compensation and stock opportunities.
• Comprehensive benefits including medical, dental, vision, life, and disability insurance.
• Retirement and financial protection benefits.
• Flexible Time Off for eligible U.S.-based exempt employees.