Role
Associate Director managing site agreements and contracts to support Summit’s global oncology clinical trials, including Phase 3 studies in NSCLC and colorectal cancer.
Responsibilities
- 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
Requirements
- 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
High-Value
- Oncology
- Phase 3
- multi-site international trials
- site negotiation
- vendor management
- regulatory compliance
- GxP knowledge
- and experience working within established clinical operations frameworks
WorkSetup
Not specified, but likely hybrid or onsite given the role’s nature.
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This position is listed as contract and hybrid.