Senior Manager, Clinical Site Partner – Italy

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Summit Therapeutics, Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

Founded 2003

🧬 Biotechnology

💊 Pharmaceuticals

🔥 Funding within the last year

💰 $500M Post-IPO Equity - Summit Therapeutics on 2025-10

Biotechnology • Pharmaceuticals

Summit Therapeutics, Inc. is a biopharmaceutical oncology company focused on the discovery, development, and commercialization of novel medicinal therapies to improve quality and duration of life for patients with serious unmet medical needs. The company is advancing ivonescimab (SMT112), a novel bispecific antibody targeting PD-1 and VEGF, through multiple Phase 3 clinical trials for non-small cell lung cancer and other solid tumors under license from Akeso. Summit emphasizes clinical development, regulatory filing strategies, and potential commercialization in its licensed territories while promoting patient- and caregiver-friendly treatment options.

📋 Description

• The Senior Manager, Clinical Operations Site Partner (CSP) is responsible for providing leadership and operational expertise in the execution of one or more Phase I–III clinical trials across the European region. • As a key member of the Global Clinical Operations (GCO) group and reporting to the Senior Director, Clinical Operations (Europe), the Senior Manager CSP plays a pivotal role in ensuring operational excellence in trial conduct and site performance. • This position serves as the primary Summit operational point of contact for assigned clinical trial sites, with full accountability for the end-to-end lifecycle of studies. • The role drives site selection, site start-up efficiency, accelerates site activation, recruitment, and maintains high standards of performance and quality throughout the study lifecycle. • The Senior Manager CSP acts as a strategic partner to sites and study teams—helping Summit achieve its vision of becoming a Sponsor of Choice by delivering a concierge-level experience to our clinical trial sites.

🎯 Requirements

• Bachelor’s degree (BA/BS) in a scientific or medical discipline required. • Advanced degree (MSc, PharmD, PhD) preferred. • Minimum of 8 years of industry experience in clinical research or related functions. • Prior experience as a Senior Clinical Research Associate (SCRA) and/or Regional/Clinical Operations Manager within a CRO or sponsor organization highly desirable. • Extensive late-stage oncology clinical trial experience required. • Proven track record of operational excellence in multi-country clinical trial management. • Strong understanding of drug development processes and regulatory environments in Europe. • Excellent interpersonal, written, and verbal communication skills in Italian and English (additional European languages a plus). • Exceptional organizational and planning abilities with demonstrated success in managing complex projects. • Strong analytical and problem-solving skills, with the ability to anticipate challenges and develop pragmatic solutions. • Understand and clearly articulate the development plan and strategic rationale. • Ability to build effective partnerships with internal stakeholders, investigators, and external partners. • Demonstrated leadership and influencing skills, with the ability to drive accountability and results. • Comfortable working independently in a fast-paced, dynamic, and global environment. • Willingness to travel up to 75% of the time within Europe and occasionally internationally.

🏖️ Benefits

• Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. • This may be different in other locations due to differences in the cost of labor. • The total compensation package for this position may also include bonus, stock, benefits and/or other applicable variable compensation.