Role Description As a Digital Content Editor, you will play a key role in driving the growth of global digital products across regions including EMEA, APAC, and India. By supporting content development, streamlining workflows, and ensuring seamless coordination between teams, you will directly contribute to delivering high-quality digital learning solutions to a global audience. Your work will help ensure that content reaches learners efficiently and effectively, enabling impactful educational experiences worldwide. This role focuses on supporting global digital product operations by managing content workflows, assisting in product development initiatives, and coordinating across regional publishing teams. Reporting to the Sr. Associate Publisher of Global Product, you will work closely with editorial, production, and digital teams to ensure timely delivery of content and successful execution of digital product strategies outside the US. What you will be doing: - Support regional publishing programs across EMEA and APAC by tracking content development progress and following up with authors. - Assist in digital content management and product development, including content commissioning responsibilities in select regions. - Coordinate with editorial teams to manage agreements, contracts, and invoice processing across regions (EMEA, APAC, India, LATAM). - Liaise with Production and Digital Production teams to monitor the status of content for digital platforms. - Track regional publishing plans and plant budgets, and provide content status updates to Product, Sales, and Marketing teams. - Ensure accessibility and accuracy of global product information for cross-functional teams. - Contribute ideas to improve editorial workflows and operational processes. Qualifications - Bachelor’s degree. - At least 3 years of experience in professional or academic publishing, or working within a university environment. - Experience in digital product development. - Strong collaboration skills with editorial, sales, and marketing teams. - Excellent written and verbal communication skills. - Exceptional organizational and multitasking abilities. - Proficiency in English (C2/C1/B2 level if not a native speaker). Requirements - Proficiency in an additional language (C2/C1/B2 level). - Experience working with Oracle systems. - Ability to travel and engage with stakeholders and authors. - Familiarity with product information management tools and strategies. Benefits - Join a global, collaborative team focused on innovation in digital learning and publishing. - Opportunity to work across international markets and contribute to impactful educational products. - Grow your expertise in digital product development. - Foster a culture of collaboration, continuous improvement, and professional growth. - Empowerment to make a meaningful difference in how content is created and delivered worldwide.

• Provide high-quality medical and scientific writing from planning and coordination through delivery of final drafts to internal and external clients • Review documents for the team and provide training and guidance to junior team members • Provide advice on document development strategy, regulations, and industry best practices • Collaborate with internal and external clients to support effective communication that results in operational excellence

We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate with purpose, hold ourselves accountable and prioritize safety and quality in everything we do. Join us and be part of something bigger – helping to simplify health care one person, one family and one community at a time. Provided to TA partner Anticipated Weekly Hours 40 Time Type Full time Pay Range The typical pay range for this role is: $60,300.00 - $132,600.00 This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, geography and other relevant factors. This position is eligible for a CVS Health bonus, commission or short-term incentive program in addition to the base pay range listed above. Our people fuel our future. Our teams reflect the customers, patients, members and communities we serve and we are committed to fostering a workplace where every colleague feels valued and that they belong. Great benefits for great people We take pride in offering a comprehensive and competitive mix of pay and benefits that reflects our commitment to our colleagues and their families. This full‑time position is eligible for a comprehensive benefits package designed to support the physical, emotional, and financial well‑being of colleagues and their families. The benefits for this position include medical, dental, and vision coverage, paid time off, retirement savings options, wellness programs, and other resources, based on eligibility. Additional details about available benefits are provided during the application process and on Benefits Moments. We anticipate the application window for this opening will close on: 04/10/2026 Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state and local laws.

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. Remote Employee Value Proposition: At Taiho Oncology, we are driven by our mission to improve the lives of cancer patients. As an Associate Director, Medical Writing, you will work on various document types and play a critical role in transforming scientific data into compelling narratives that contribute to innovative cancer treatments. Join a dedicated team that fosters a collaborative, patient-first environment, where your expertise and passion will directly impact patient care and advance oncology research. We believe in empowering our employees through continuous learning, career development, and a supportive culture that values diverse perspectives and encourages innovation. If you are ready to take on new challenges and make a meaningful difference, Taiho Oncology offers you the opportunity to grow, excel, and be a part of something bigger. Together, we are relentless in our pursuit of better cancer treatments. Join us in putting patients at the heart of everything we do. Position Summary: The incumbent is responsible for authoring Taiho Oncology, Inc., (TOI), documents submitted to Regulatory Authorities including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and relevant summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions for drugs in line with regulatory requirements and internal standard operating procedures. Performance Objectives: - Responsible for authoring TOI documents submitted to Regulatory Authorities (e.g. FDA and EMA) including Clinical Study Reports, Investigator Brochures, Protocols, Protocol Amendments, Briefing Documents, Health Authority responses, and clinical summary sections of Common Technical Documents (CTDs) in support of worldwide (outside of Asia) regulatory submissions. - Prepare documents in line with regulatory requirements in conjunction with Regulatory Affairs and with internal standard operating procedures in a timely and accurate manner. - Understand publishing standards for FDA and MAA. - Manages and oversees medical writing deliverables assigned to internal and contract writers or other third party vendors. - Represent Global Medical Writing department on clinical development cross-functional teams and project initiatives. - Develop and implement medical writing processes in line with SOPs. - Prepares project and/or status reports. - Proficient in Microsoft applications and document management systems. Education/Certification Requirements: - Bachelor’s Degree in life science, health-related or pharmaceutical field, or the equivalent in experience. Advanced degree preferred. Knowledge, Skills, and Abilities: - Minimum of 8 years combined experience in academic/clinical and/or industry setting writing clinical protocols, CSRs and/or medical and/or scientific documents. - Extensive previous experience in Medical Writing in clinical drug development, preferably some experience in oncology. - Familiarity with the regulatory submission process, ICH and GCP guidelines and recommendations. - Knowledge of template development, document management systems and requirements - Experience developing and implementing medical writing processes for all stages of clinical development. - Strong working knowledge of medical writing requirements and document components. - Good interpersonal skills that involves working well in a team environment and the ability to lead others. - Good organizational and planning skills; drive for results. - Ability to read, analyze and interpret scientific and technical information. - Effective analytical/problem solving skills. The pay range for this position at commencement of employment is expected to be between $194,650 - $229,000 annually. 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 annual bonus/incentive comp plans, potential long term incentive plan, 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 a candidate/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-Remote 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 email People@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.