About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company with over 35 years of dedication to creating a healthier world. Headquartered globally, Gilead has transformed lives through groundbreaking therapies for HIV, viral hepatitis, COVID-19, and cancer. The company's relentless pursuit of innovation extends to inflammatory diseases, ensuring access to life-changing treatments worldwide. At the heart of Gilead's mission is collaboration, determination, and a drive to address the biggest health challenges. Employees are empowered as key contributors to scientific discoveries, with a strong emphasis on inclusive leadership and professional growth.

Gilead's Impact in HIV, Oncology, and Inflammatory Diseases

Gilead pioneered HIV treatments, making antiretroviral therapies widely available and improving patient outcomes dramatically. In oncology, innovative drugs target cancers with precision, while advancements in inflammatory diseases alleviate chronic suffering. The Pediatric Center of Excellence in Dublin amplifies these efforts, focusing on child-specific solutions.

Role Overview

The Senior Director, Global Regulatory Affairs Liaison – Pediatric Center of Excellence, is a pivotal leadership role at Gilead's global hub in Dublin, Ireland. As Franchise Lead for Regulatory Affairs, you will spearhead strategies for pediatric developments across Virology, Oncology, and Inflammation therapeutic areas. This position demands strategic partnership with cross-functional teams and regulatory authorities to secure licensure and optimal market access for pediatric products. Serving as a senior regulatory expert, you will drive submissions, monitor commitments, and foster continuous improvement in GRA capabilities.

Key Responsibilities

In this role, you will be accountable for the oversight and leadership of global pediatric regulatory strategies, ensuring successful completion of submissions and deliverables. Key duties include developing and optimizing regulatory processes in collaboration with Global TA teams, representing Gilead in authority negotiations, and proactively managing risks with mitigation plans. You will manage direct reports, provide resource recommendations, and lead initiatives on the Global TA Regulatory Liaison leadership team. Additionally, you will advise the Pediatric Center of Excellence on site management and special projects to advance pediatric therapies.

Strategic Leadership in Pediatric Regulatory Affairs

Expect to guide global pediatric plans, prepare submissions, and track progress across therapeutic areas, aligning with broader product goals for efficiency and compliance.

Qualifications & Requirements

Ideal candidates hold an advanced degree in life sciences, pharmacy, medicine, or a related discipline, coupled with 15+ years of regulatory affairs experience, including substantial pediatric focus. Expertise in Virology, Oncology, and Inflammation is essential, alongside proven leadership in global teams and direct interactions with regulatory bodies like EMA and FDA. Strong skills in strategic planning, risk management, cross-functional collaboration, and mentorship are required. Familiarity with Gilead's portfolio and GRA processes is highly advantageous.

Leadership and Technical Expertise

You must excel in developing regulatory strategies, managing budgets, and driving process innovations while ensuring adherence to policies and regulations.

Benefits & Perks

Gilead offers a premium compensation package, including a competitive salary estimated at €180,000–€250,000 annually, performance bonuses, and equity opportunities. Comprehensive health insurance, retirement savings plans, and family benefits support work-life balance. Employees enjoy professional development programs, leadership training, and flexible hybrid work in Dublin. Additional perks include wellness programs, generous paid time off, and access to cutting-edge facilities at the Pediatric Center of Excellence.

Career Growth

At Gilead, career progression is a priority. As a People Leader, you will shape culture and empower teams, with opportunities to advance into executive regulatory roles or broader corporate leadership. Mentorship programs, global rotations, and tuition reimbursement foster continuous learning. The Pediatric Center of Excellence provides a platform for high-visibility projects, positioning you as a key influencer in biopharma regulatory affairs.

Why Join Gilead

Joining Gilead means contributing to therapies that save pediatric lives in HIV, oncology, and beyond. Dublin's vibrant hub offers a collaborative environment with world-class resources. Be part of a mission-driven culture where innovation thrives, inclusion is paramount, and every role drives global health impact. With bold ambitions and employee-centric leadership, Gilead equips you to make a difference.

Role FAQs

Q: What therapeutic areas does this role cover? A: Virology, Oncology, and Inflammation, with a pediatric focus.
Q: Is relocation support available? A: Gilead provides comprehensive support for international hires to Dublin.
Q: What level of experience is required? A: 15+ years in regulatory affairs, with senior leadership exposure.
Q: Does the role involve direct reports? A: Yes, managing one or more team members.
Q: How does this position interact with regulators? A: As Gilead's contact, you will negotiate and represent in key interactions.
Q: Is the role hybrid or on-site? A: Flexible hybrid model at the Dublin Pediatric Center of Excellence.