Director Product Management

About the role

The Director of Product Management, RIM at Veeva leads a team of Product Managers dedicated to the Veeva RIM platform, owning the end-to-end journey for regulatory offerings. This role is responsible for defining and communicating the product strategy and roadmap for regulatory solutions aimed at enhancing process efficiency for both internal and external customers. The position involves designing solutions that translate complex compliance requirements into clear team momentum while working closely with engineering to execute the vision. You will craft product narratives and shape build artifacts that guide engineers on modular architecture, specifically for audit trails and regulatory clarity. Leading review rituals ensures that documentation meets the necessary compliance clarity standards is a core function of this position. You will coordinate ship schedules, balancing market urgency with risk mitigation logic to ensure timely and responsible delivery. Forging partner roadmaps that align external vendors with platform interoperability goals is essential to maintaining a cohesive ecosystem. Championing improvement loops to extract signals from user behavior and support patterns will drive continuous iteration and product refinement. Guarding quality thresholds by validating release readiness against regulatory checklists is required to maintain the highest standards. You will enable customer success by creating training artifacts that clarify feature interaction paths and regulatory workflows.

Key facts

What you'll do

• Conduct discovery sessions with regulatory stakeholders to capture nuanced requirements for Veeva RIM offerings.
• Translate regulatory constraints and compliance language into intuitive user workflows that reduce friction for life sciences teams.
• Define the strategic vision for regulatory product offerings while aligning engineering and customer teams around shared outcomes and measurable success metrics.
• Design intake workflows that capture regulatory questions proactively, preventing issues from escalating into larger compliance concerns.
• Shape build artifacts that provide engineers with clear guidance on modular architecture, focusing on robust audit trails and data integrity.
• Lead review rituals with cross-functional teams to ensure documentation meets compliance clarity standards and addresses real-world usage scenarios.
• Coordinate ship schedules by assessing dependencies, balancing market urgency with risk mitigation logic to ensure high-quality releases.
• Forge partner roadmaps that align external vendors with platform interoperability goals, ensuring seamless integration across the regulatory ecosystem.
• Champion improvement loops by analyzing user behavior and support patterns to extract actionable signals for product iteration and enhancement.
• Guard quality thresholds by validating release readiness against regulatory checklists and compliance requirements before public deployment.
• Enable customer success through the creation of training artifacts that clarify feature interaction paths and demonstrate compliance workflows.
• Collaborate with Life Sciences industry experts to bring the next generation of Veeva products to market with innovative regulatory solutions.
• Maintain a deep understanding of life sciences processes, including trials, safety, and pharmacovigilance, to inform product decisions and roadmap priorities.
• Communicate effectively with executive and technical audiences, presenting complex regulatory concepts in a clear and actionable manner.

Requirements

• Bring 3-5 years of experience managing complex product initiatives in regulated environments, demonstrating a history of successful delivery.
• Exhibit deep familiarity with life sciences processes, including trials, safety, and pharmacovigilance, to ensure product strategies reflect industry realities.
• Possess a proven ability to translate regulatory constraints into intuitive user workflows that simplify compliance for end users.
• Demonstrate strong written and verbal communication skills to effectively engage both executive leadership and technical engineering teams.
• Show commitment to understanding and navigating the complexities of regulatory landscapes within the life sciences sector.
• Display the capability to work independently and collaboratively within a cross-functional, mission-driven organization.
• Have experience aligning product strategy with business objectives in a fast-growing SaaS environment.
• Exhibit strong analytical and problem-solving skills to address challenges in regulatory product management.

Nice to have

• Experience with cloud platforms serving compliance, risk, or quality domains is highly desirable for this role.

Practical notes

• This is a full-time position based in Massachusetts
• Boston.
• Please review the official apply page for specific information regarding remote policy, exact compensation details, and start date availability.
• The duties and responsibilities outlined here are derived from the source material and should be confirmed on the official application page for The Director Product Management role at Veeva represents a significant opportunity to influence the future of regulatory information management within the life sciences industry. The successful candidate will play a critical role in ensuring that Veeva's RIM platform continues to meet the highest standards of regulatory compliance while driving efficiency for customers. This position requires a strategic thinker who is equally comfortable diving into technical architecture and articulating the broader product vision to diverse audiences. You will be instrumental in shaping how regulatory questions are captured, managed, and resolved within the Veeva ecosystem. The role demands a balance of creativity and rigor, ensuring that solutions are both innovative and compliant with established standards. Collaboration with life sciences experts ensures that the products remain grounded in real-world needs and regulatory expectations. Continuous improvement is central to the position, requiring a mindset focused on extracting insights and driving iterative enhancements. Quality and compliance remain at the forefront of all responsibilities, ensuring that every release meets stringent regulatory checklists. This is a leadership position that offers the chance to make a tangible impact on the life sciences industry and the delivery of therapies to patients worldwide.