The Director will lead strategic sourcing, contracting, and vendor governance for clinical operations and global clinical trial portfolios. They will partner with cross-functional teams to optimize study-related spending, manage supplier performance, and ensure compliance across the clinical development lifecycle.
Lead medical affairs and clinical development across multiple oncology programs, including directing Phase 1–3 trials, shaping study strategy, and supporting trial execution and milestones. Collaborate with internal teams and external investigators, contribute to regulatory submissions and safety reviews, and guide scientific communications and clinical documents.
The Director, Clinical Scientist leads the design and execution of hematology/oncology clinical studies while collaborating with cross-functional teams. They are responsible for authoring regulatory documents, managing data quality, and fostering relationships with investigators and clinical sites.
The Regional Marketing Director will develop and execute regional marketing strategies and customer engagement initiatives to support the commercialization of the oncology portfolio. They will act as a key partner to cross-functional teams, including Sales and Medical Affairs, to translate national brand strategies into effective regional execution.
The Director of Market Access Payer Account 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.
The Director leads the global clinical operations analytics strategy, overseeing performance metrics, data governance, and the Veeva Vault Clinical platform. They translate operational data into actionable insights to drive study execution, resource planning, and risk-based decision-making across the organization.
The Corporate Counsel will draft, review, and negotiate a wide range of clinical and commercial contracts to support business objectives and mitigate risk. They will also act as a liaison between internal departments and external parties to ensure efficient legal and contractual operations.
The Associate Director will prepare, edit, and finalize high-quality clinical and regulatory documents to support global development programs. They will also manage document review processes and collaborate with cross-functional teams to ensure regulatory compliance and timely deliverables.
The Senior Director provides global regulatory leadership and strategic oversight for Chemistry, Manufacturing, and Controls (CMC) activities across the company's oncology portfolio. This role is responsible for defining global regulatory strategies for biologics and leading interactions with global Health Authorities to ensure successful product development and licensure.
The Medical Science Liaison acts as a field-based scientific expert responsible for developing territory plans and fostering relationships with healthcare professionals in the oncology space. They provide disease state education, support clinical development initiatives, and communicate complex scientific data to internal and external stakeholders.
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 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 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 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 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 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 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 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 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 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.
