--- title: 'Associate Director, Risk Based Quality Management Lead at Summit Therapeutics' canonical: 'https://feeny.ai/job/associate-director-risk-based-quality-management-lead-summit-therapeutics-vt6at0qnxewm' type: 'job' last_seen: '2026-09-11' --- # Associate Director, Risk Based Quality Management Lead at Summit Therapeutics - **Company:** Summit Therapeutics - **Location:** Princeton New Jersey, United States - **Compensation:** $174k–$204k - **Posted:** 2026-08-06 - **Last confirmed live:** 2026-09-11 - **Apply:** https://job-boards.greenhouse.io/summittherapeutics/jobs/4356283009 ## Job description 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. Overview of Role: The Associate Director, Risk-Based Quality Management (RBQM Lead) is accountable for the operational execution of RBQM activities across assigned clinical studies. Serving as the primary RBQM subject matter expert within study teams, this role implements and maintains study-level risk management, centralized monitoring, Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), targeted monitoring strategies, and risk review processes. Working closely with Clinical Operations, Clinical Science, Data Management, Biostatistics, Medical Monitoring, and CRO partners, the RBQM Lead proactively identifies, evaluates, escalates, and mitigates risks throughout the clinical trial lifecycle to support participant safety, data reliability, and regulatory compliance. Role and Responsibilities: Study-Level RBQM Execution - Serve as the RBQM Lead and core study team member from protocol development through study closeout - Lead RBQM planning, execution, and ongoing risk oversight throughout study conduct. - Develop and maintain study-specific RBQM Plans and Critical-to-Quality (CtQ) factors, ensuring alignment with protocol objectives and identified study risks. Risk Assessment & Risk Management - Facilitate cross-functional risk identification and assessment workshops and lead creation and maintenance of study Risk Assessment and Categorization Tools (RACTs). - Document, score, track, and periodically reassess risks, identifying new or emerging risks from study performance data and operational signals. - Collaborate with study teams to implement risk mitigation strategies and actions, monitor their effectiveness, and recommend additional interventions when needed. ## Key Risk Indicator (KRI) Management - Develop and maintain study-specific KRIs linked to identified risks and CtQ factors, including thresholds, triggers, and escalation pathways. - Review and interpret KRI outputs and investigate threshold breaches and root causes. - Facilitate study-team RBQM reviews and track KRI trends, actions, and mitigation outcomes. Quality Tolerance Limit (QTL) Oversight - Collaborate with study teams to establish protocol-specific QTLs - Monitor QTL performance throughout study conduct. - Investigate QTL excursions and assess potential impact on participant safety and data integrity. - Coordinate documentation of investigations, assessments, and corrective actions. - Present QTL findings during study governance reviews. Central Monitoring: - Lead the implementation of centralized monitoring strategies across multiple clinical trials - Monitor and review clinical trial data across sites to ensure accuracy, completeness, and consistency with study protocols. - Conduct routine centralized monitoring reviews, through performing real-time data surveillance to identify outliers, trends, and potential issues that could impact data integrity. - Analyze data visualizations, listings, dashboards, and statistical outputs. - Identify unusual data patterns, quality concerns, and site-specific risks. - Evaluate trends across subjects, sites, countries, and regions. - Assess effectiveness of ongoing monitoring activities. - Generate risk summaries and recommendations for study teams. - Escalate significant findings requiring additional oversight. - Conduct risk-based monitoring activities, such as assessing site performance, patient safety data, and identifying sites at risk of data discrepancies or protocol violations. - Utilize central monitoring tools and platforms (e.g., RBQM, EDC, CTMS) to track study progress and ensure data consistency. - Support data query resolution by coordinating with site and CRO teams and ensuring timely data corrections. Study Risk Review Meetings - Lead recurring study risk review meetings to update the RACT and risk registers and facilitate cross-functional risk-management decisions. - Prepare dashboards and study risk summaries and present significant risk signals, KRI trends, QTL status, and mitigation activities. - Track decisions and action items and ensure timely follow-up. Site Risk Surveillance - Review site-level risk profiles and identify high-risk sites requiring additional oversight. - Partner with Clinical Operations, CRO teams, CRAs, Data Management, Medical Monitoring, and other stakeholders to develop and implement site-specific action plans. - Monitor the effectiveness of interventions at high-risk sites and escalate persistent quality concerns. Issue Management & CAPA Support - Support investigations of significant quality events and compliance issues, including root cause analyses. - Contribute to the definition of corrective and preventive actions (CAPAs) and quality improvement plans and monitor the effectiveness of proposed actions throughout the conduct of the study. Inspection Readiness - Maintain inspection-ready documentation of risk assessments, KRI and QTL reviews, centralized monitoring activities, findings, corrective actions, and recommendations. - Support sponsor audits, regulatory inspections, and quality-control checks, including preparation of RBQM-related responses and data-review reports. - Prepare monitoring reports summarizing findings, trends, and recommendations for improvements to the study team in support of the preparation for internal and regulatory audits - Ensure RBQM activities comply with GCP, ICH guidelines, FDA regulations, and other applicable regulatory requirements. - Participate in internal quality assurance activities and continuous improvement initiatives. Experience, Education and Specialized Knowledge and Skills: - Bachelor’s degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical-related areas preferred. - 10+ years of clinical operations experience in sponsor pharmaceutical or biotechnology organizations. - 7+ years of direct RBQM, centralized monitoring, risk-based monitoring, clinical quality, or study management experience. - Experience supporting global Phase II and/or Phase III clinical trials. - Experience conducting risk assessments; developing and managing KRIs and QTLs; and facilitating risk review meetings. - Demonstrated ability to interpret complex scientific, clinical, and operational data to identify quality and compliance risks and support centralized trial monitoring. - Experience working with CROs, RBQM technology and clinical analytics platforms. - Proven ability to oversee large, complex studies managed in-house and through CRO partners. - Demonstrated sound judgment and problem-solving ability related to regulatory requirements, external partners, timelines, and complex clinical programs. - Excellent planning, communication, negotiation, and organizational skills. - Strong knowledge of the drug development process, ICH guidelines, and GCP, with a deep understanding of clinical trial execution and the ability to apply this knowledge to complex global studies. This is the pay for this position Pay Transparency $174,000—$204,000 USD 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 recruiting@smmttx.com 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. ## About Summit Therapeutics ## Company Overview - **One-liner**: Summit Therapeutics Inc. is a biopharmaceutical oncology company focused on discovering, developing, and commercializing novel bispecific antibody therapies, with its lead candidate ivonescimab targeting PD-1 and VEGF for multiple solid tumors. - **Entity Type**: Public (NASDAQ: SMMT) - **Headquarters**: Miami, Florida, USA (with additional offices in Palo Alto, CA; Princeton, NJ; Oxford, UK; and Dublin, Ireland) - **Founded**: 2003 - **Founders**: Not publicly disclosed on the company website; the company was founded in 2003. ## Core Business - **Primary industry**: Biopharmaceuticals / Oncology - **Target customers**: B2B (healthcare providers, patients, and caregivers) with a focus on resolving serious unmet medical needs in oncology - **Mission statement**: "To resolve serious, unmet medical needs for the betterment of overall human health." [smmttx.com](https://smmttx.com/company/about-us/default.aspx) ## Products & Services - **Ivonescimab (SMT112)**: A novel, potential first-in-class investigational bispecific antibody targeting both PD-1 and VEGF. It is designed to combine immunotherapy (PD-1 blockade) with anti-angiogenesis (VEGF blockade) into a single molecule. Currently being studied in several global Phase 3 clinical trials for non-small cell lung cancer (NSCLC), colorectal cancer (CRC), and head and neck squamous cell carcinoma (HNSCC). Licensed from Akeso, Inc. (HKEX: 9926.HK) for territories including the U.S., Canada, Europe, Japan, Latin America, the Middle East, and Africa. [smmttx.com](https://smmttx.com/pipeline/default.aspx) ## Market Standing - **Valuation/Market Cap**: Approximately $2.7 billion (as of recent data) [linkedin.com](https://www.linkedin.com/company/summit-therapeutics) - **Key Metric**: Annual revenue of approximately $705,000 (reported). The company is pre-commercialization and heavily investing in R&D. Total funding raised since IPO (2015) is not disclosed, but the company has a strong cash position from equity offerings. - **Notable Investors/Partners**: Akeso, Inc. (key licensing partner for ivonescimab). The company is publicly traded with institutional and retail investors. - **Growth Signals**: - Headcount grew 72.5% year-over-year to 244 employees. [linkedin.com](https://www.linkedin.com/company/summit-therapeutics) - Multiple global Phase 3 trials actively recruiting (HARMONi, HARMONi-3, HARMONi-7, HARMONi-GI3, ILLUMINE). - Over 4,000 patients have been treated with ivonescimab across all clinical trials globally. [smmttx.com](https://smmttx.com/pipeline/default.aspx) - Achieved Great Place to Work® Certification. [smmttx.com](https://smmttx.com/careers/careers-overview/default.aspx) ## Competitive Advantages - **Novel Mechanism**: Ivonescimab is a first-in-class bispecific antibody targeting both PD-1 and VEGF simultaneously, potentially offering superior efficacy and fewer side effects compared to combination therapies. - **Speed and Execution**: The company emphasizes "high-speed execution in commercialization" and has rapidly initiated multiple Phase 3 trials. - **Global Reach**: Licensed territories cover major markets (U.S., Canada, Europe, Japan, Latin America, Middle East, Africa) with a strong partner (Akeso) in the rest of the world. - **Strong Balance Sheet**: With a $2.7B market cap and public listing, the company has access to capital markets to fund its pipeline. ## Strategic Focus - **Current priorities**: Advancing ivonescimab through Phase 3 clinical trials across multiple solid tumor indications (NSCLC, CRC, HNSCC), with the goal of regulatory approval and commercialization. - **Future direction**: Expanding the pipeline into additional solid tumors and leveraging the bispecific platform for future therapies. The company is focused on becoming a leading oncology player. - **Near-term milestones**: Data readouts from ongoing Phase 3 trials, potential regulatory submissions, and building commercial infrastructure. ## Why Work Here - **Culture**: The company has achieved Great Place to Work® Certification, indicating a positive, supportive, and fulfilling work environment. Core values include Commitment to People, Integrity, Passion for Excellence, Purposeful Urgency, Accountability, and Collaboration. [smmttx.com](https://smmttx.com/careers/careers-overview/default.aspx) - **Work Environment**: Fast-paced, high-energy atmosphere focused on innovation and collaboration. The company emphasizes "making a significant difference in patients’ lives." - **Benefits (U.S.)**: - 401(k) with 6% employer match - Employee Stock Purchase Plan (ESPP) with 15% discount up to the annual federal limit - Flexible Spending Account - Commuter Benefit - Onsite lunch provided - **Benefits (U.K.)**: - Private Medical Insurance - Employee Assistance Program - Life Assurance Policy - Company Pension Contributions - ESPP - **Remote/Hybrid Policy**: Not explicitly stated, but multiple office locations suggest a hybrid or on-site presence is expected for many roles. - **Open Roles**: 25 active job postings (as of recent data) including Senior Director of Sales Operations, Clinical Scientists, Medical Science Liaisons, and Drug Product MSAT roles. [greenhouse.io](https://job-boards.greenhouse.io/summitherrapeutics) - **Headcount Growth**: 72.5% year-over-year growth signals a scaling organization with opportunities for career advancement. ## Sources 1. [smmttx.com - About Us](https://smmttx.com/company/about-us/default.aspx) 2. [smmttx.com - Investor Relations Overview](https://www.smmttx.com/overview/default.aspx) 3. [smmttx.com - Pipeline](https://smmttx.com/pipeline/default.aspx) 4. [smmttx.com - Careers Overview](https://smmttx.com/careers/careers-overview/default.aspx) 5. [linkedin.com - Summit Therapeutics Company Page](https://www.linkedin.com/company/summit-therapeutics) 6. [greenhouse.io - Summit Therapeutics Careers](https://job-boards.greenhouse.io/summitherrapeutics) ## Other roles at Summit Therapeutics - [Senior Director, Regulatory CMC](https://feeny.ai/job/senior-director-regulatory-cmc-summit-therapeutics-united-states-qnq72sd971hr) — United States - [National Account Director, Government Payers —Medicaid](https://feeny.ai/job/national-account-director-government-payers-medicaid-summit-therapeutics-field-1sjzqhpn2hwe) — Field, United States - [Sr. Clinical Data Scientist](https://feeny.ai/job/sr-clinical-data-scientist-summit-therapeutics-palo-alto-y90jqt03ag43) — Palo Alto, CA - [Sr. Manager, Clinical Quality Assurance](https://feeny.ai/job/sr-manager-clinical-quality-assurance-summit-therapeutics-remote-0mexn4fh8bg8) - [Senior Director, Regional Marketing](https://feeny.ai/job/senior-director-regional-marketing-summit-therapeutics-princeton-nj-85z6bke8tkv2) — Princeton NJ, United States - [Senior Manager, Commercial Analytics](https://feeny.ai/job/senior-manager-commercial-analytics-summit-therapeutics-princeton-nj-s8drfzyv2fvy) — Princeton NJ, United States - [Associate Director, Regulatory Affairs](https://feeny.ai/job/associate-director-regulatory-affairs-summit-therapeutics-united-states-6v4qz21pkcxj) — United States - [Chief Commercial Officer](https://feeny.ai/job/chief-commercial-officer-summit-therapeutics-princeton-nj-y6mzyr8j1web) — Princeton NJ, United States - [Associate Director, Clinical Study Start-Up](https://feeny.ai/job/associate-director-clinical-study-start-up-summit-therapeutics-princeton-new-nemvsnpnzfdd) — Princeton New Jersey, United States - [Senior Director, Program Management](https://feeny.ai/job/senior-director-program-management-summit-therapeutics-palo-alto-california-fwf6t8kayq3v) — Palo Alto California, United States