Director, Clinical Operations
Summit Therapeutics
Director, Clinical Operations
Summit Therapeutics
Develops and commercializes therapeutic medicines
About Summit:
Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs. At Summit, we believe in building a team of world class professionals who are passionate about this mission, and it is our people who drive this mission to reality. Summit’s core values include integrity, passion for excellence, purposeful urgency, collaboration, and our commitment to people. Our employees are truly the heart and soul of our culture, and they are invaluable in shaping our journey toward excellence.
Summit’s team is inspired to touch and help change lives through Summit’s clinical studies in the field of oncology. Summit has multiple global Phase 3 clinical studies, including:
Non-small Cell Lung Cancer (NSCLC)
HARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI.
HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
HARMONi-7: Phase 3 clinical study which is intended to evaluate ivonescimab monotherapy compared to pembrolizumab monotherapy in patients with first-line metastatic NSCLC.
Colorectal Cancer (CRC)
HARMONi-GI3: Phase 3 clinical study intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy.
Ivonescimab is an investigational therapy not presently approved by any regulatory authority other than China’s National Medical Products Administration (NMPA). Summit is headquartered in Miami, Florida, and has additional offices in California, New Jersey, the UK, and Ireland.
DIRECTOR, CLINICAL OPERATIONS
Overview of Role:
The Director, Regional Clinical Operations, Middle East, provides strategic leadership, operational expertise, and regional influence to enable the successful execution of Summit Phase I–III oncology clinical trials across the Middle East region. The role is part of the Global Clinical Operations (GCO) organization and reports directly to the Senior Director, Clinical Operations Europe.
This position serves as the senior clinical operations leader for the region and is accountable for driving country-startup strategy, site activation excellence, stakeholder engagement, and operational delivery across all countries within the region. The Director will leverage extensive regional expertise, established relationships with oncology investigators, sites, institutions, regulatory authorities, ethics committees, and healthcare stakeholders to accelerate trial approvals and study execution.
The scope of this role includes all countries within the Middle East region and may expand to neighbouring countries based on business needs and portfolio requirements.
Role and Responsibilities:
Regional Leadership & Strategy
· Lead and drive operational excellence for clinical trial execution across the Middle East region.
· Accountable for regional performance against study startup, enrolment, quality, timeline, and budget commitments.
· Act as the primary regional escalation point for operational challenges impacting study delivery.
· Develop regional operational strategies that maximize speed, quality, patient access, and investigator engagement.
· Provide strategic recommendations regarding country selection, site placement, and regional investment decisions.
External Stakeholder Engagement
· Establish and maintain senior-level relationships with regulatory agencies, ethics committees, health authorities, hospital leadership, research networks, cancer centers, and professional organizations throughout the region.
· Influence key external stakeholders involved in clinical trial approvals and activation to support efficient regulatory and operational pathways.
· Represent the company at regional scientific meetings, investigator meetings, industry organizations, and external stakeholder forums.
· Monitor and influence emerging regulatory and clinical research trends that may impact oncology development programs within the region.
· Serve as a trusted partner to investigators and institutions to strengthen the company's sponsor reputation and long-term strategic presence.
Investigator & Site Network Leadership
· Maintain a comprehensive and current understanding of leading oncology institutions and investigators across all countries within the Middle East.
· Utilize an extensive network of investigator and site relationships to strengthen feasibility assessments and support rapid study startup.
· Partner with global study teams to identify high-performing sites capable of delivering complex oncology protocols.
· Drive initiatives that improve site experience, site retention, and long-term engagement.
Feasibility & Start-up
· Lead regional feasibility strategy and provide expert country-level operational intelligence.
· Ensure robust assessment of regulatory pathways, site capabilities, patient populations, and competitive trial landscapes.
· Influence country startup strategies to optimize timelines and regulatory approval success rates.
· Identify regional barriers to activation and implement proactive mitigation strategies.
· Ensure timely incorporation of regional insights into global study plans.
Operational Oversight
· Maintain oversight of regional study performance and proactively identify risks to timelines, enrolment, quality, or budget.
· Partner with Global Study Teams to develop and implement mitigation plans for regional operational challenges.
· Ensure regional activities are conducted in compliance with GCP, local regulations, company policies, and applicable health authority requirements.
· Support inspection readiness activities and provide regional expertise during audits and inspections.
Experience, Education and Specialized Knowledge and Skills:
· BA/BS required; advanced degree (MS, PharmD, PhD, MBA) preferred.
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.
Summit does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact Summit’s Talent Acquisition team at [email protected] to obtain prior written authorization before referring any candidates to Summit.
Summit Therapeutics Inc. is an Equal Opportunity Employer and takes pride in creating and maintaining diverse environment. We do not discriminate in recruitment, hiring, training or promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
Develops and commercializes therapeutic medicines
Summit Therapeutics conducts end-to-end drug development, from identifying promising candidates to regulatory approval and commercialization. It relies on an in-house team of scientists and administrators and uses selective partnerships to advance products. Its therapies aim to improve both quality and length of life for patients with serious health needs. By controlling the development and commercialization process in-house, Summit seeks to speed development, reduce costs, and build a lasting healthcare organization with strong market presence and value for patients, clinicians, caregivers, and shareholders.
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