The Senior Clinical Trial Manager provides strategic leadership and operational oversight for complex global oncology clinical trials from start-up through closeout. They are responsible for managing CRO relationships, ensuring regulatory compliance, and driving patient enrollment and data quality strategies.
The Clinical Trial Manager II oversees all aspects of global clinical trial execution, including site selection, activation, and monitoring. They partner with CROs to ensure data quality, regulatory compliance, and adherence to study timelines and protocols.
The Associate Director provides operational leadership for global clinical trial execution, overseeing vendor performance and cross-functional team collaboration. They are responsible for ensuring study delivery within budget and compliance with regulatory standards while managing clinical operations staff.
The Director, Safety Physician provides medical oversight for pharmacovigilance activities, including the review of individual case safety reports and signal detection. They also lead safety-related medical input for clinical studies and ensure compliance with global regulatory requirements.
The National Account Director will lead and manage Fee-for-Service and Managed Medicaid accounts to ensure broad access, reimbursement, and patient affordability for oncology products. This role involves building relationships with key decision-makers and executing state-level access strategies while collaborating with cross-functional teams.
The Senior Manager of Clinical Quality Assurance will collaborate with cross-functional teams to provide GxP compliance advice and manage clinical site and vendor audits. They are responsible for overseeing end-to-end quality management, coordinating CAPAs, and preparing program teams for health authority inspections.
The Medical Science Liaison acts as a field-based scientific expert, strategically supporting oncology therapeutic objectives and communicating scientific data to healthcare professionals. They are responsible for developing territory engagement plans, supporting clinical research initiatives, and fostering relationships with external experts.
The Medical Science Liaison acts as a field-based scientific expert to support oncology therapeutic objectives and communicate scientific data to healthcare professionals. They are responsible for developing territory plans, managing expert relationships, and providing disease state education across the product lifecycle.
The Medical Science Liaison serves as a field-based scientific expert responsible for communicating Summit Therapeutics' oncology science to healthcare professionals. They develop territory plans, support clinical research initiatives, and foster relationships with external experts to meet scientific and business objectives.
The Medical Science Liaison serves as a field-based scientific expert responsible for building relationships with healthcare professionals and supporting the company's oncology therapeutic objectives. They provide disease state education, support clinical research initiatives, and act as a conduit for scientific insights between the field and internal cross-functional teams.
The Medical Science Liaison serves as a field-based scientific expert, strategically supporting oncology therapeutic objectives and communicating scientific data to healthcare professionals. They are responsible for developing territory engagement plans, supporting clinical research initiatives, and fostering relationships with external experts.
The Medical Science Liaison serves as a field-based scientific expert responsible for communicating complex oncology data to healthcare professionals and supporting clinical development initiatives. They develop territory plans, foster relationships with external experts, and provide disease state education to support the company's scientific and business objectives.
The Director, Value Outcomes Liaison will cultivate relationships with population-based decision makers to communicate the clinical and economic value of ivonescimab. They will collaborate with internal teams to execute scientific engagement strategies and ensure the inclusion of the therapy in clinical and payer pathways.
The Director, Value Outcomes Liaison will cultivate relationships with US population-based decision makers to communicate the clinical and economic value of ivonescimab. They will collaborate with internal teams to execute scientific engagement strategies and ensure the inclusion of the therapy in clinical and payer pathways.
The Senior Director leads, coaches, and develops a national team of Medical Science Liaisons to ensure high-quality, compliant scientific engagement. They translate therapeutic area strategy into regional execution while overseeing medical insights to inform evidence generation and lifecycle planning.
The Director of Medical Writing will produce high-quality, strategically aligned regulatory documents to support clinical development programs. They will manage document review processes, coordinate with cross-functional teams, and ensure compliance with global regulatory requirements.
The Sr. Commercial Attorney will lead the drafting and negotiation of commercial, marketing, and market access agreements to support the company's product launches. They will also provide legal advice on distribution networks, regulatory compliance, and complex reimbursement strategies.
The Medical Science Liaison acts as a field-based scientific expert to support oncology therapeutic objectives and build relationships with healthcare professionals. They are responsible for executing territory plans, supporting clinical research initiatives, and providing disease state education.
The Senior Director of Regulatory Affairs leads global regulatory strategies for oncology products, overseeing IND/CTA approvals and marketing applications. They also provide regulatory leadership, mentor team members, and ensure compliance with relevant laws and guidelines.
The Key Accounts Director is responsible for establishing strategic relationships with IDNs, Academic Centers, and health systems to ensure optimal market access for oncology medicines. They will lead account strategy, negotiate contracts, and collaborate cross-functionally to accelerate clinical pathway inclusion and resolve reimbursement barriers.
The Director of Market Access Payer Accounts is responsible for managing national and sub-national payer accounts to ensure broad access, reimbursement, and patient affordability for oncology products. This role involves building relationships with key decision-makers, executing access strategies, and collaborating with internal teams to support product positioning.
Lead the commercialization and launch of ivonescimab in the East Coast region by managing a team of oncology account managers. Execute national sales strategies and collaborate with cross-functional partners to achieve regional market share goals.
Oversee global Phase 3 clinical trials and BLA filings, focusing on protocol design and medical oversight. Lead cross-functional teams to execute clinical development goals and manage investigator engagements.
Lead global regulatory strategies to secure IND/CTA approvals and manage the planning and execution of global marketing applications (BLA/MAA) for oncology products. Act as the primary regulatory lead for development collaborations, partnerships, and cross-functional alignment across clinical and commercial teams.
