Director, Clinical Study

Associate Director managing site agreements and contracts to support Summit’s global oncology clinical trials, including Phase 3 studies in NSCLC and colorectal cancer.

• develop pricing strategies
• negotiate and finalize site contracts and budgets
• collaborate with legal, finance, CROs, and sites
• ensure compliance with regulatory standards
• analyze budgets for cost-effectiveness
• support site activation and vendor relationships
• monitor progress and performance metrics
• implement departmental processes and strategies
• resolve disputes
• and contribute to trial efficiency

• Bachelor's in Life Sciences, Business or related
• 10+ years’ experience in clinical trial site agreement management within biotech or pharma, with oncological trial exposure preferred
• strong global negotiation skills
• budget development and financial acumen
• experience with multi-site, multi-vendor global trials
• proficiency with MS Office and document management
• excellent communication, organizational, and analytical skills

• Oncology
• Phase 3
• multi-site international trials
• site negotiation
• vendor management
• regulatory compliance
• GxP knowledge
• and experience working within established clinical operations frameworks

Not specified, but likely hybrid or onsite given the role’s nature.