SSU Manager: Feasibility & Site Contracts

Summit Therapeutics Inc.

Princeton, Northern (NJ, KY)

Hybrid

USD 139,000 - 163,000

Full time

5 days ago
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Job summary

Summit Therapeutics Inc. is seeking an experienced SSU Manager to oversee feasibility, site start-up and budget negotiations for global Phase 2/3 trials. This role builds relationships with CROs, sites and internal stakeholders to drive site activation and ensure compliant study start-up delivery.

The ideal candidate has extensive SSU and feasibility experience, strong contract negotiation skills, and can lead cross-functional teams in a fast-paced biotech setting.

Qualifications

  • Degree in Life Sciences, Business Administration or related field; equivalent experience considered.
  • 5–7 years for manager; 10+ years for Sr. Manager in feasibility, SSU, site agreements.
  • Knowledge of clinical trial conduct, including multi-center, global trials.
  • Strong knowledge of ICH/GCP guidelines and regulatory requirements.
  • Excellent interpersonal, written and verbal communication, admin and computer skills.
  • Experience with process improvement initiatives; cross-functional collaboration.

Responsibilities

  • Lead day-to-day SSU operations to meet goals in line with GCP/ICH.
  • Negotiate and finalize site agreements and budgets.
  • Provide up-to-date project status and financial information in tracking systems.
  • Present the budget to senior leaders for approval with full detail.
  • Collaborate with Legal, Finance and Clinical teams on site agreements.
  • Develop SSU strategy and manage activation timelines.

Skills

Feasibility studies
Site contracts
Budgeting
Negotiation
Cross-functional collaboration

Education

Life Sciences / Business Administration degree

Tools

MS Office
Electronic document management systems
Document review tools

Job description

Summit Therapeutics Inc. is seeking an experienced SSU Manager to oversee feasibility, site start-up and budget negotiations for global Phase 2/3 trials. This role builds relationships with CROs, sites and internal stakeholders to drive site activation and ensure compliant study start-up delivery.

The ideal candidate has extensive SSU and feasibility experience, strong contract negotiation skills, and can lead cross-functional teams in a fast-paced biotech setting.

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