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)
Colorectal Cancer (CRC)
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:
Reporting to the VP of Patient Safety & Pharmacovigilance (PSPV), the Safety Physician Director will be responsible for investigational and marketed product pharmacovigilance activities. Primary responsibilities include medical review of individual case safety reports (ICSRs), strategic input for adverse event monitoring and signal detection, ensuring global pharmacovigilance regulatory requirements are met, and safeguarding patients enrolled in our trials or administered our products.
Role and Responsibilities:
- Implement the medical review of ICSRs (narratives, coding, expectedness, causality and seriousness) to ensure quality reports. Evaluate medical accuracy of ICSRs reports.
- Prepare Analysis of Similar Events (AOSE) for IND safety reports.
- Confirm criteria and content for expedited reporting and unblinding (e.g. SUSAR or urgent safety issues).
- Lead or actively contribute to the preparations and presentation of safety information to the Drug Safety Committee (DSC), Product Safety Review Team (PSRT), Independent Data Monitoring Committees (IDMCs), and other internal and external stakeholders/parties, when required.
- Interact and liaise with PV vendor medical reviewer and Summit Medical Monitors.
- Review individual and aggregate safety data from safety database on a scheduled basis for signal detection.
- Act as product lead and/or therapeutic area lead as assigned.
- Share ICSR case quality issues with PV Operations as appropriate, and support Quality Assurance of ICSR medical review.
- Implement appropriate case follow up / queries per SOPs.
- Develop and support medical coding conventions, and systematic process improvements for ICSR medical review.
- Support reconciliation between Safety and Clinical databases.
- Develop, maintain, update, review and approve list of expected terms via the Reference Safety Information (RSI) in the IB, in collaboration with development partner and cross-functional teams.
- Act as a Medical Safety Review process lead and support the development, training on and implementation of new processes in Medical Safety Review.
- Mentor junior medical safety reviewers as needed and applicable, provide direct managerial responsibilities for medical safety reviewers on therapeutic or functional team.
- Maintain a state of inspection readiness, and act as functional representative and point of contact for Health Authority Inspection and Internal Process Audits within the remit of role and responsibility.
- Provide expertise and guidance on teams for interdepartmental and cross-functional initiatives including process improvement, standards development, Standard Operating Procedures (SOP) creation, and metrics with regards to medical safety review.
- Author, review and/or approve safety content of various aggregate safety summary documents such as DSURs, PBRERs, Regulatory Response documents, Safety Signal Evaluation documents, etc., when requested.
- Perform other duties related to the position as necessary as defined in SOPs or as requested by their supervisor.
- All other duties as assigned
Experience, Education and Specialized Knowledge and Skills:
- MD/DO or international equivalent plus a minimum of 8+ years relevant work as a safety physician.
- Working knowledge of case management and medical review processes and procedures.
- Clinical knowledge of oncology therapeutic area patient populations and drug classes (immunotherapy and chemotherapy). Oncologist with practical experience is preferred.
- Proficiency in technical safety systems.
- Strong knowledge and understanding of global safety reporting and pharmacovigilance requirements, aggregate reporting, and signal detection in both clinical trials and post market safety.
- Experience in safety data analysis and writing study related narratives, aggregate reports and safety assessments.
- Demonstrated ability to work effectively in a team environment (including Safety, Clinical Development, Medical Affairs, Clinical Operations, and Regulatory), as well as independently.
- Experience in MedDRA coding and search strategies.
- Strong computer and database skills.
- Attention to detail, accuracy and confidentiality.
- Clear and concise oral and written communication skills.
- Excellent organizational, critical thinking, and problem-solving skills.
- Must be able to effectively multi-task and manage time-sensitive and highly confidential documents.
- Communicate effectively and articulate complex ideas in an easily understandable way.
- Prioritize conflicting demands.
- Work in a fast-paced, demanding and collaborative environment.
