Gilead Sciences Inc

Manager, Regulatory Affairs

Gilead Sciences Inc$133K — $172K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree with 6+ years or Master's Degree with 4+ years in Regulatory Affairs or related field.
  • Experience supporting Promotional Review Committee processes.
  • Strong understanding of FDA advertising and promotion regulations.
  • Management experience with Form FDA 2253 and FDA APLB/OPDP submissions.
  • Expertise in claims management, reference governance, and annotation standards.

Responsibilities

  • Lead and evolve Claims, References, and Annotation programs.
  • Partner with various stakeholders to document and maintain claims.
  • Monitor compliance with reference formatting standards and approved claims.
  • Develop and deliver training materials for Regulatory Affairs and PRC Operations.
  • Maintain PRC Operations playbooks and documentation of processes.
  • Schedule and quality-check FDA submissions with cross-functional teams.
  • Analyze PRC Operations metrics and recommend process improvements.

Benefits

  • Company-sponsored medical, dental, and vision insurance plans.
  • Life insurance coverage.
  • Potential eligibility for a discretionary annual bonus.
  • Access to stock-based long-term incentives based on role.
  • Paid time off and comprehensive benefits package.
Full Job Description
Job Description

The PRC Operations team under Regulatory Affairs Advertising and Promotion serves as a strategic operational partner to Legal, Medical Affairs, Commercial, and agency partners by enabling efficient, compliant, and scalable execution of Kite's Promotional Review Committee (PRC) process. This role will lead key operational programs supporting promotional material review, claims and reference governance, FDA submission readiness, training, business process optimization, and performance reporting. This individual will also collaborate with cross-functional stakeholders to help identify and advance automation and AI technology into the PRC Process.

Key Responsibilities

Claims, References, and Annotation Governance
  • Lead the maintenance and evolution of Kite's Claims, References, and Annotation programs.
  • Partner with Medical, Legal, Regulatory, Commercial, and agency stakeholders to ensure claims are appropriately documented and maintained.
  • Monitor compliance with internal reference formatting standards, submission requirements, and approved claims usage.
  • Drive continuous improvements to claim management processes, reference libraries, reusable text assets, and associated documentation.


Training and Communications
  • Develop, maintain, and deliver PRC Operations and Regulatory Affairs Advertising & Promotion training materials.
  • Create and update training decks, new hire onboarding materials, process documentation, and business guidance resources.
  • Facilitate training sessions for business owners, agency partners, reviewers, and operational stakeholders.
  • Monitor process adoption and identify opportunities for additional education and training.


Playbooks and Process Documentation
  • Own and maintain PRC Operations playbooks, job aids, standard operating procedures, business process guides, and submission guidelines.
  • Coordinate cross-functional reviews and updates to process documentation.
  • Ensuring documentation reflects evolving regulatory requirements, system enhancements, and business processes.
  • Support inspection readiness and audit preparedness activities through documentation governance.


FDA Submission Operations
  • Schedule, prepare, and quality check submissions to FDA.
  • Manage submission timelines and collaborate with cross-functional teams to ensure accurate and timely submissions.


Business Metrics and Operational Excellence
  • Enhance, maintain, and analyze PRC Operations metrics and dashboards.
  • Generate routine reporting for leadership and executive stakeholders.
  • Monitor performance indicators, identify trends, and recommend process improvements.
  • Leverage data-driven insights to improve operational efficiency, quality, and compliance.


Automation and Digital Innovation
  • Evaluate opportunities to leverage artificial intelligence (AI), automation, and digital solutions to improve PRC Operations processes.
  • Identify operational bottlenecks and recommend scalable technology solutions.
  • Partner with Information Technology, Regulatory Affairs, Commercial Operations, and external vendors to advance automation initiatives.
  • Support implementation and optimization of systems such as Veeva PromoMats, eCTD capabilities, reporting solutions, and future technology platforms.


Leadership and Stakeholder Management
  • Lead cross-functional operational projects and serve as a trusted advisor to key stakeholders.
  • Foster a culture of continuous improvement, collaboration, accountability, and innovation.


Basic Qualifications

  • Bachelor's Degree AND 6+ years of experience in Regulatory Affairs, Promotional Review Operations, Commercial Operations, Medical Affairs Operations, Regulatory Business Operations, or related pharmaceutical/biotechnology functions OR
  • Master's Degree AND 4+ years of experience in Regulatory Affairs, Promotional Review Operations, Commercial Operations, Medical Affairs Operations, Regulatory Business Operations, or related pharmaceutical/biotechnology functions


Preferred Qualifications
  • Experience supporting Promotional Review Committee (PRC), Medical Review Committee (MRC), or comparable review processes.
  • Strong understanding of FDA advertising and promotion requirements.
  • Experience managing Form FDA 2253 and FDA APLB/OPDP submissions.
  • Experience with Veeva PromoMats/MedDocs and promotional material lifecycle management.
  • Demonstrated expertise in claims management, reference governance, and annotation standards.
  • Experience developing training curricula, playbooks, process documents, and operational guidance materials.
  • Strong analytical capabilities and experience developing operational metrics and dashboards.
  • Knowledge of AI, automation technologies, workflow optimization, and digital transformation initiatives.
  • Demonstrated project management and stakeholder management skills within a highly matrixed environment.
  • Demonstrated ability to be flexible and adaptable to change
  • Strong interpersonal skills and understanding of team dynamics
  • Excellent written, verbal, presentation, and organizational skills.


Success Profile

The ideal candidate combines strong operational execution with strategic thinking and is recognized as a trusted business partner who can:
  • Drive operational excellence across PRC-related processes.
  • Translate complex requirements into scalable business processes.
  • Leverage technology and automation to improve efficiency.
  • Build effective cross-functional partnerships.
  • Deliver high-quality, compliant outcomes while supporting an evolving business environment.


The salary range for this position is: $133,195.00 - $172,370.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

About Gilead Sciences Inc

Gilead Sciences is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet need. With each new discovery and experimental drug candidate, they seek to improve the care of patients suffering from life-threatening diseases. Gilead's primary areas of focus include HIV/AIDS, liver disease, and serious cardiovascular and respiratory conditions.

Gilead Sciences Inc Careers

Join the vibrant team at Gilead Sciences Inc, a leader in the biopharmaceutical industry known for its innovative approach to healthcare. At Gilead, we are committed to advancing the care of patients around the globe through rigorous science and research.

Work You’ll Do

Embark on a career journey with Gilead Sciences Inc, where job opportunities abound in a variety of fields, from scientific research to marketing and sales. Our team is dedicated to fostering an environment of diversity and inclusion, where every employee can thrive.

Innovate and Lead

At Gilead, innovation is at the core of everything we do. Join us and contribute to our mission of saving lives through advanced treatments and cutting-edge medicine. Our leadership is committed to nurturing professional growth, making Gilead an ideal place for those who aim to lead and innovate in the healthcare industry.

Grow Your Career

Gilead Sciences Inc offers a wealth of career advancement opportunities. With personalized career development programs, employees are encouraged to pursue their professional interests and expand their skills. Whether through on-the-job learning, formal training, or leadership development, we provide the tools necessary for long-term career growth.

Be Part of Our Team

Our team at Gilead Sciences Inc is composed of passionate, curious, and solution-driven professionals. By joining us, you’ll collaborate with some of the brightest minds in the industry. Our culture promotes teamwork and an interdisciplinary approach to problem-solving, making our workplace dynamic and innovative.

Internship and Employment Opportunities

Start your career with Gilead through our internship programs, which offer hands-on experience in biopharmaceutical development and business operations. For seasoned professionals, our employment opportunities span across various disciplines, inviting you to bring your valuable skills to our team.

Benefits and Culture

Gilead Sciences Inc is not only a great place to work but also offers competitive benefits designed to support the health, well-being, and financial security of our employees and their families. From health insurance to retirement plans and wellness programs, we ensure our team members are taken care of.

Networking and Professional Development

We emphasize the importance of networking and professional development within the company. Regular workshops, seminars, and training sessions are held to enhance your skills and knowledge. Additionally, Gilead’s strong emphasis on internal networking allows for cross-departmental collaboration and innovation.

Join Our Hiring Events

Stay connected with Gilead by joining our hiring events and exploring open positions that match your skills and interests. We are always on the lookout for dedicated, creative, and driven team players. Prepare your resume, ace the interview, and take the first step towards a fulfilling career at Gilead Sciences Inc.

Explore Jobs at Gilead Sciences Inc

Discover the exciting career opportunities waiting for you at Gilead Sciences Inc. Visit our careers page to search for open positions, read about our company culture, and learn how you can make a difference in the global healthcare landscape.

Stay Up to Date

Keep informed with the latest company news, career tips, and industry insights—all from the people who work at Gilead Sciences Inc. Subscribe to our job alert emails and personalize your experience to receive updates that align with your career preferences. Join Gilead Sciences Inc today and be part of a team that values innovation, leadership, and a commitment to diversity and employee growth.
Learn more about Gilead Sciences Inc
Size
14,400 employees
Market Cap
$107.2 billion
Industry
Net Income
$123 million
Founded
1987
5 Year Trend
-2.1%
Revenue
$24.6 billion
NASDAQ

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