About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company dedicated to creating a healthier world for all people. For over 35 years, Gilead has pioneered therapies for some of the world's most challenging diseases, including HIV, viral hepatitis, COVID-19, cancer, and inflammatory diseases. Our relentless pursuit of innovation has led to life-changing treatments that improve lives and ensure global access to cutting-edge medicine. With a mission-driven culture, Gilead fosters collaboration, determination, and bold ambition. Employees are at the heart of our success, driving scientific discoveries in HIV treatments like Biktarvy, oncology breakthroughs, and therapies for inflammatory conditions. Join us to make a direct impact on global health.

Role Overview

As Director, R&D Information Systems at Gilead Sciences, you will serve as a thought leader in the Regulatory and R&D Quality Systems organization. This role focuses on supporting Regulatory Affairs and R&D Quality stakeholders, particularly in regions outside the U.S., by providing visibility into requirements that enhance business processes. Based in Cambridge or Stockley Park, UK, with 3 days onsite per week, you will drive innovation through current technology trends, including AI, to transform how Gilead meets corporate objectives. This leadership position demands expertise in Regulatory Information Management (RIM), submission management, inspection readiness, and more, positioning you at the forefront of biopharma digital transformation.

Strategic Impact

In this role, you will partner with global teams to introduce innovative technologies, manage critical system escalations, and represent Gilead during inspections. Your enterprise mindset will ensure systems evolve to support Gilead's ambitious goals in HIV, oncology, and inflammatory diseases research.

Key Responsibilities

Lead with expertise and vision in this pivotal role:

• Deliver guidance on RIM, submission management, inspection readiness, and AI technologies, applying an enterprise-wide perspective.
• Manage escalations during system outages, collaborating with IT and business leaders for clear impact assessment and user communication.
• Act as Gilead's representative in inspections and audits, while mentoring UK-based Development Systems team members.
• Drive evaluation of emerging technologies to meet evolving business needs and serve as SME on cross-functional requirement gathering.
• Engage senior leaders, provide strategic input to department planning, and lead projects across Regulatory Affairs, R&D Quality, Patient Safety, and IT.

Qualifications & Requirements

To excel as Director, R&D Information Systems, candidates must demonstrate:

• BA/BS in a scientific discipline, information systems, or equivalent with 12+ years managing Regulatory Affairs systems; or MS with 10+ years.
• Proven success driving change in complex organizations via new technologies and processes.
• In-depth knowledge of RIM technologies, AI transformations, computer system validation, and change management.
• Extensive pharma/biotech experience, including global/regional roles in Regulatory Affairs and R&D Quality.
• Strong leadership, self-starter mindset, cross-functional collaboration, and exceptional communication skills.

Key Competencies

Ideal candidates navigate ambiguity, inspire innovation, and deliver results through teamwork and strategic vision.

Benefits & Perks

Gilead Sciences offers a premium compensation package designed to attract top talent:

• Competitive base salary estimated at $180,000-$250,000 USD annually, plus bonuses and equity.
• Comprehensive health, dental, and vision insurance with wellness programs.
• Generous 401(k) matching, paid time off, and family leave policies.
• Professional development opportunities, including leadership training and tuition reimbursement.
• Hybrid work model with onsite collaboration in state-of-the-art facilities.

Career Growth

At Gilead, people leaders are central to our culture of inclusion and empowerment. This Director role offers a platform for advancement into executive R&D IT leadership, with exposure to global projects in HIV, oncology, and inflammatory diseases. Benefit from mentorship, cross-functional projects, and Gilead's commitment to employee aspirations. Our track record shows rapid progression for high performers in biopharma innovation.

Why Join Gilead

Gilead is more than a biopharma leader—it's a force for global health equity. Contribute to therapies transforming HIV care, advancing oncology treatments, and addressing inflammatory diseases. Work in a collaborative environment with cutting-edge resources, onsite 3 days weekly in Cambridge or Stockley Park. Be part of a team relentless in pursuit of 'possible,' with every role playing a critical part in scientific breakthroughs. Gilead's bold ambitions create unparalleled opportunities for impact and growth.

Role FAQs

Q: What is the work arrangement?
A: Hybrid model requiring 3 days onsite per week in Cambridge or Stockley Park, UK.

Q: What experience is essential?
A: 10-12+ years in Regulatory Affairs systems, with pharma/biotech background and AI/RIM expertise.

Q: How does this role support Gilead's mission?
A: By innovating systems for R&D Quality and Regulatory Affairs, enabling faster development of HIV, oncology, and inflammatory disease therapies.

Q: What leadership opportunities exist?
A: Mentor teams, lead projects, and influence strategic planning across global functions.

Q: Is relocation support available?
A: Gilead offers competitive relocation packages for qualifying candidates.