Senior Trial Manager (Sponsor Dedicated) (Clinical Research)

TL;DR

Senior Trial Manager (Sponsor Dedicated) (Clinical Research): Provides oversight and trial management of clinical trials from planning, execution to completion with an accent on regulatory compliance, team coordination, and milestone achievement. Focus on developing monitoring plans, site and vendor selection, and optimizing clinical monitoring for quality and timely deliverables.

Location: United States, Eastern Time Zone preferred

Salary: $122,000 USD starting base pay

Company

Clinical research organization helping biotech, medtech, and specialty pharma companies bring new medicines, devices, and diagnostics to patients.

What you will do

• Provide oversight and manage planning, execution, and completion of clinical trials per ICH/GCP regulations.
• Coordinate trial operations team to achieve milestones and project delivery.
• Develop and review project documentation including CRFs, study plans, protocols, and informed consents.
• Create and maintain clinical monitoring plans (CMP) with escalation instructions.
• Evaluate and select investigative sites and vendors, ensuring timely site activation within budget.
• Lead and monitor clinical monitoring team, review data reports, and address quality issues.

Requirements

• Bachelor’s degree in clinical, biological, scientific, or health-related field (or equivalent)
• 10 years clinical research experience, including 7 years study oversight
• Proven customer experience delivery and task ownership
• Excellent English verbal and written communication skills
• Strong analytical, organizational skills; ability to manage multiple projects in fast-paced environment
• Eastern Time Zone preferred

Culture & Benefits

• Comprehensive benefits package including health insurance, retirement plans, and paid time off.
• Opportunities for growth, skill development, and work-life balance.
• Flexible environment where ideas influence work and voice matters.
• Equal opportunity employer compliant with federal guidelines.