Intern, Project Management Princeton, NJ, USA Req #400 Friday, February 7, 2025 Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our 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: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us. Hybrid Employee Value Proposition: This internship offers a unique opportunity for a motivated college student to gain hands-on experience in clinical development project management by participating in initiatives and global product development teams within a dynamic and collaborative environment. We are committed to providing a valuable learning experience and mentorship to support professional development and growth. Position Summary: + The intern will work closely with our team of project management professionals to support various aspects of clinical drug development including strategic planning among global, cross-functional projects designed and coordinated to achieve the organization’s strategy. Performance Objectives: + Support project planning efforts for global development programs under the direction of the Global Project Management Lead. + Communicate and collaborate with project management department members and functional global development team members within the organization. + Support Project Management organization and Global Product Development Team initiatives, including process improvement, monitoring of objectives/goals and tracking deliverables. + Manage project timeline and budget for a drug development project and ensure the project scope is aligned across various tracking and reporting systems. + Attend team meetings, training sessions, and other department activities as needed. + Adhere to all relevant regulatory guidelines, protocols, and standard operating procedures (SOPs) to ensure compliance with industry standards. Education/Certification Requirements: + Currently enrolled in a Bachelor's degree program in a relevant science, business or math field. Knowledge, Skills, and Abilities: + Strong interest in product development strategy and business operations of the drug development process, including clinical research development spanning Phase I-IV. + Desire to participate in complex pharmaceutical projects and initiatives in a multi-disciplinary, global matrix team environment. + Ability to work independently, as well as collaboratively within a team environment. + Prior knowledge of global drug development, QA, mfg. ops, clinical & regulatory functions preferred but not required. + Proficiency in Microsoft Office applications, particularly Excel, Word, and PowerPoint. + Familiarity with Project planning tools preferred. The incumbent in this position may be required to perform other duties, as assigned. The pay range for this position at commencement of employment is expected to be between $18 to $22 per hour. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, commissions, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. #LI-Hybrid Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please emailPeople@taihooncology.com. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records. The incumbent in this position may be required to perform other duties, as assigned. + Princeton, NJ, USA