Head of US Risk Management & Product Safety (REMS)

Job Description Summary

Job Description Summary
As the Head of US Risk Management & Product Safety (Risk Evaluation and Mitigation - REMS) you will lead the US safety strategy behind some of Novartis’ most complex and high-impact medicines. You will own the end-to-end design and execution of Risk Evaluation and Mitigation Strategies, shaping how patients safely access innovative therapies across the United States.

In this influential role, you’ll partner closely with FDA and senior cross-functional leaders, drive inspection-ready operations, and translate evolving regulatory expectations into practical, patient-centric risk management that enables confident, compliant commercialization.

 

Job Description

Major accountabilities:

1.     REMS Strategy & Leadership

• Lead the US REMS Safety Strategy, ensuring alignment with FDA requirements, global risk management plans, and evolving patient safety priorities. 

• Drive development, approval, and launch of innovative, commercially feasible REMS programs including restricted distribution, prescriber/pharmacy certification, and patient enrollment systems. 

•  Provide US input into Risk Management Plans (RMPs) and REMS assessments; ensuring the implementation of recommendations and continuous optimization of risk minimization measures. 

2.     REMS Operational Oversight

• Manage REMS vendor performance (including call centers, specialty pharmacies, prescriber certification platforms) to ensure compliance, high quality training, and robust data integrity. 

• Oversee execution of REMS commitments and risk mitigation activities.

3.     US Local Product Safety Management

• Oversee US safety related labeling (USPI, Medication Guides, REMS safety language) and oversee timely, accurate submission of US aggregate reports (e.g., PADERs, PBRERs). 

• Serve as the primary contact for US product safety inquiries, escalations, and Health Authority requests. 

4.     Regulatory Compliance & Quality Oversight

• Maintain readiness for inspections and audits; manage findings, corrective actions, and CAPAs to closure.

• Keep current with evolving regulatory requirements and provide insights to support REMS and safety risk management strategy. 

• Participate in FDA interactions, REMS negotiations, advisory boards, and industry forums. 

Essential Requirements:

• Fluent English (both spoken and written).

• A Bachelor’s degree required. An advanced degree is preferred (PharmD, M.D, PHD).

• 10+ years' experience in risk management operations, including risk management planning and leadership experience in the pharmaceutical industry required.

• 4+ years of REMS management and/or risk management experience in a matrix role that encompasses leading cross-functional teams across all areas of an organization

• Strong knowledge of FDA REMS requirements, US PV regulations, risk minimization strategies, and audit/inspection management.

• Proven leadership in cross-functional settings; excellent communication, influencing, collaboration, and decision-making skills.

• Strong executive presence with excellent interpersonal, verbal, and written communication abilities, organizational acumen, and the capability to manage multiple high‑priority projects simultaneously.

• Proven expertise leading large-scale, strategic initiatives related to drug development, risk management and regulatory requirement.

• Deep understanding of risk management principles and best practices for REMS development implementers, and experience implementing risk management practices and/or managing risk in complex and/or conflict related environments.

Desirable Skills:

• Familiarity with safety databases, REMS platforms, and data analytics tools.

Novartis Compensation and Benefit Summary 

The salary for this position is expected to range between $204,400 and $379,600 per year. 

The final salary offered is determined based on factors like relevant skills and experience and may be reviewed periodically. Novartis may change the published salary range based on company and market factors.  Compensation includes a performance-based cash incentive and eligibility for annual equity awards. 

US-based eligible employees receive a comprehensive benefits package including health, life, disability benefits, 401(k) with company match, and generous time off. 

Join Novartis and play a defining role in advancing patient safety and regulatory excellence in the United States.  Apply now to be part of a purpose-driven organization reimagining medicine for patients worldwide. 

 

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. 

 

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

 

Salary Range

$204,400.00 - $379,600.00

 

Skills Desired

Clinical Research, Clinical Trials, Functional Teams, Leadership, Medical Strategy, Process Safety Management, Regulatory Compliance, Risk Management, Safety Science