Director, Clinical Trial Management - Oncology

Responsibilities

• Manage and provide accountability for day-to-day operations of oncology clinical trials in accordance with ICH/GCP and applicable regulations
• Serve as the primary Sponsor contact for operational project-specific issues and study deliverables
• Provide cross-functional oversight of internal project team members and ensure all necessary project-specific training is completed
• Develop operational project plans and manage risk assessment and execution
• Review and provide input for study protocols, edit check specifications, data analysis plans, and final study reports
• Manage study vendors, site quality, and monitoring deliverables
• Maintain in-depth knowledge of protocols, therapeutic areas, and specific indications

Requirements

• Bachelor’s degree in a health-related field
• 5+ years of experience as a project or clinical trial manager within a CRO environment
• Proven experience managing clinical trials across Phases 1-4
• Experience with project timeline management
• Experience participating in bid defense meetings
• Strong leadership and mentoring skills

Preferred Qualifications

• Advanced degree in a health-related field

Benefits

• Competitive compensation and benefits package
• Competitive PTO packages
• Flexible work environment
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. Headquartered in Cincinnati, Ohio, we employ more than 6,000 people across 40+ countries.