layiq

/la·yiq/adjective

worthy; deserving; fitting; suitable.

A role, opportunity, or path that merits attention, time, and pursuit.

LAYIQ - Senior Director: Global Patient Safety Solutions Partner at Regeneron Pharmaceuticals

In this role, you will own platform strategy and delivery for Regeneron's Global Patient Safety technology portfolio, leading a team of Directors across the domain. Your day-to-day responsibilities will include:
GPS Platform Strategy & Ownership
Partner with senior GPS leadership, to align technology and capabilities to deliver on Global Patient Safety objectives and enterprise priorities.
Own and prioritize, in partnership with the business, the multi-year platform strategy and roadmap for Argus (safety), PIVIT, Signal Management, aRMM/ARMM, and SRP, translating Global Patient Safety and regulatory priorities into a funded, prioritized delivery plan.
Own the organizational design of the GPS Business Solution function, including structure, role allocation, and resourcing across Directors and Managers assigned to the domain.
Establish governance frameworks, standards, and validation practices for GPS platform delivery, ensuring consistency across teams and vendor engagements.
Own budget, forecast, and vendor contract accountability for the GPS platform portfolio, including software licensing and services agreements.
Delivery Oversight & Team Leadership
Serve as the escalation and quality-assurance point for planning, prioritization, and execution of safety platform initiatives led by direct reports.
Oversee product backlog, incident management, and release governance across the GPS platform portfolio, ensuring consistent reporting of value delivered against plan.
Coach and develop Directors and Managers, ensuring delivery commitments are met and domain capabilities continue to mature.
Manage steering committee meetings, working groups, and issue/release management for upgrades to existing safety platforms.
Data Governance & Regulatory Compliance
Partner with GPS business leadership, Regulatory Affairs, and Quality organizations to ensure safety platforms meet GxP validation, data integrity, and audit-readiness standards.
Own data classification, access, and quality standards for safety-related data, ensuring compliance with global safety reporting obligations (e.g., FDA, EMA).
Maintain oversight of case processing, signal detection, and risk management workflows to ensure platforms support timely and accurate regulatory reporting.
Cross-Functional & Vendor Partnership
Partner with Enterprise IT, Enterprise Architecture, and Information Security to align safety platform investments with enterprise standards and security requirements.
Build and maintain relationships with key platform vendors to clarify demands, resolve conflicts, and align technology roadmaps to business needs.
Represent GPS technology priorities in enterprise architecture and governance forums, ensuring alignment with enterprise-wide standards.
Executive & Stakeholder Engagement
Serve as the primary point of contact for senior GPS and IT leadership on matters requiring negotiation of complex or ambiguous issues.
Build relationships with key GPS business leaders to clarify demands, resolve conflicts, and align technology roadmaps with pharmacovigilance priorities.
Monitor industry trends in drug safety technology and regulatory reporting, bringing forward innovative approaches to senior leadership.
Prepare and deliver executive-level materials on the health and roadmap of the GPS platform portfolio for governance forums and senior leadership.

Education & Experience
Bachelor’s degree in Computer Science, Information Systems, Business Administration, or a related field (Master’s degree preferred).
15+ years of progressive industry/relevant professional experience, including significant experience managing enterprise-scale Global Patient Safety, drug safety, or regulatory technology platforms.
Experience in the biotech, pharma, or life sciences industry strongly preferred.
Proven experience leading a multi-disciplinary team of Directors and Managers, including budget and vendor contract accountability for a major function.
Technical Expertise
Deep expertise in patient safety and drug safety systems (e.g., Oracle Argus Safety, signal management, and risk management platforms).
Experience with global safety reporting standards and regulatory requirements (e.g., E2B, ICSR, FDA, EMA).
Strong knowledge of GxP validation practices and solution delivery life cycle management.
Experience managing technology capability identification, selection, and implementation across multiple simultaneous safety platform initiatives.
Skills & Competencies
Proven track record of budget and vendor management for a department or major function.
Strong stakeholder management and negotiation skills, with experience influencing senior management internally and externally.
Demonstrated ability to grow, motivate, and develop teams, coaching Directors and Managers through career milestones and progression.
Strategic mindset with the ability to define organizational structure and set long-term goals and objectives for a major function.
Exceptional executive communication skills, with experience engaging senior/executive leadership on sensitive or ambiguous matters.
Certifications (Preferred)
PMP or equivalent project/program management certification.
ITIL or SAFe Agile certification.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.

Senior Director: Global Patient Safety Solutions Partner

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