Director, Regulatory Compliance

About the role

Taiho Oncology is seeking a Director, Regulatory Compliance (Promotional Review Committee) to serve as a strategic partner supporting compliant, effective external communications across a growing oncology portfolio while helping strengthen and streamline Taiho Oncology’s promotional review capabilities.

Responsibilities

• Serve as the Regulatory Compliance representative for the Promotional Review process, including participation in the Promotional Review Committee (PRC).
• Review promotional, non-promotional, scientific exchange, and educational materials for regulatory compliance.
• Contribute to interpretation of FDA regulations, guidance documents, enforcement trends, and industry standards related to advertising and promotion.
• Partner with Marketing, Medical Affairs, Legal, Compliance, Market Access, and Sales to facilitate compliant and effective communications.
• Advise business partners on promotional strategy, claim development, and risk mitigation.
• Support launch planning and review of promotional campaigns for new products and indications.
• Assist in preparing responses to FDA inquiries related to promotional activities.
• Monitor regulatory developments and communicate emerging requirements and enforcement trends to internal stakeholders.
• Contribute to process improvements that enhance PRC effectiveness, efficiency, and consistency.
• Provide training and education to cross-functional partners regarding promotional regulations and review requirements.
• Support audits, inspections, and compliance assessments involving advertising and promotion activities.
• Collaborate with external regulatory consultants as needed.

Requirements

• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Regulatory Affairs, or related discipline required.
• Advanced degree, such as PharmD, PhD, MS, MBA, or JD, preferred.
• Minimum 10 years of pharmaceutical or biotechnology industry experience.
• Significant Regulatory Affairs experience with direct responsibility for promotional review and advertising and promotion compliance.
• Oncology experience strongly preferred.
• Demonstrated participation in a Promotional Review Committee, Medical Legal Regulatory review committee, or similar review process.
• Experience working with commercial organizations and cross-functional teams supporting marketed products.
• Strong knowledge of FDA regulations governing pharmaceutical advertising and promotion, including OPDP requirements, promotional guidance documents, and enforcement actions.
• Ability to interpret complex regulatory requirements and provide practical business guidance.
• Excellent communication, influencing, relationship-building, analytical, and risk-assessment skills.
• Ability to balance regulatory compliance with business objectives and work effectively in a fast-paced, matrixed environment.
• Excellent project management and organizational skills.
• Proficiency in promotional review systems and workflows.
• Experience supporting multiple oncology brands, specialty pharmaceutical products, digital and social media materials, market access, patient support programs, product launches, or lifecycle management initiatives preferred.

Pay

The pay range for this position at commencement of employment is expected to be between $217,600 and $256,000 annually. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

Benefits

The total compensation package for this position may include other elements, including annual bonus/incentive compensation 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).