Manager, Medical Information & Operations

Taiho Oncology, Inc.•Princeton, NJ

1d•$147,900 - $174,000•Hybrid

About The Position

Taiho Oncology is on a mission to improve the lives of patients with cancer, their families, and caregivers. Their “People first” approach means they also highly value their employees. Taiho’s success is founded on ensuring they always act with accountability, collaboration, and trust. By following these guiding principles, they earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, they are working on cutting-edge science and growing their portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities empower them to innovate and touch the lives of more and more patients. It’s their work, their passion, and their legacy. They invite you to join them.

Requirements

PharmD, RN, or other advanced degree in life sciences required.
3–5 years of experience in Medical Information, Medical Affairs, or a related pharmaceutical function is required.
Demonstrated experience participating in or supporting medical review is required.
Strong scientific, clinical, and regulatory knowledge with the ability to critically evaluate and communicate complex data clearly.
Excellent written and verbal communication skills; demonstrated proficiency communicating across all levels of the organization.
Proven ability to work cross-functionally and build effective stakeholder relationships in a matrixed environment.
Ability to manage multiple competing priorities in a fast-paced, deadline-driven environment.
Prior experience with AI tools and supporting the implementation of AI-driven solutions to improve Medical Information processes is necessary.

Nice To Haves

Licensure or certification in a health sciences field preferred.
Experience in oncology or specialty therapeutics is preferred.

Responsibilities

Serve as the primary point of contact to receive, document, and respond to unsolicited medical inquiries.
Utilize scientific expertise to prepare, update, and maintain medical information resources for assigned products.
Perform medical and scientific review of promotional and scientific exchange materials within the Medical Review Committee in partnership with Medical Directors, ensuring the highest standards of scientific accuracy and regulatory compliance.
Identify and implement continuous improvement initiatives to enhance MI efficiency, quality, and scalability.
Analyze metrics and develop insights reports on Medical Information activities for presentation to internal stakeholders.
Provide scientific support for assigned stakeholders on ad hoc projects and initiatives, including at Medical Information booths at assigned medical conferences.
Contribute to the development and maintenance of MI policies, guidelines, and SOPs in adherence to applicable FDA guidance and company compliance standards.