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, and cancer. The company's relentless pursuit of innovation has resulted in groundbreaking treatments that improve lives and expand access to care globally. Gilead's work extends to oncology and inflammatory diseases, where it continues to develop transformative medicines. With a mission-driven culture, Gilead fosters collaboration, determination, and bold ambition, making it a top destination for life sciences professionals.

Role Overview

The Sr Clinical Trials Manager position at Gilead Sciences in Seoul, South Korea, is a pivotal leadership role within the Clinical Operations team. This role involves leading Phase I-IV clinical trials across Gilead's therapeutic areas, ensuring compliance with SOPs, policies, and regulatory guidelines. You will provide strategic oversight to clinical studies within designated programs, managing budgets, timelines, and cross-functional teams. This position offers the opportunity to drive high-quality clinical data supporting global product registration and commercialization, while contributing to Gilead's fight against major health challenges.

Strategic Impact

As a Sr Clinical Trials Manager, you will partner with Clinical Program Managers to define study logistics and plans, incorporating best practices to achieve objectives efficiently. Your expertise will influence study protocols, case report forms, and informed consents, ensuring seamless execution from start-up to close-out.

Key Responsibilities

In this role, you will take ownership of critical clinical trial components:

• Lead and oversee all aspects of assigned studies in collaboration with Clinical Program Managers.
• Actively manage clinical study budgets with proactive financial oversight.
• Lead CRO and vendor selection, managing interactions and deliverables.
• Collaborate cross-functionally to align on study goals and ensure project success.
• Provide guidance, training, and oversight to team members, CROs, vendors, and investigators.
• Define and enforce study timelines, monitoring compliance with protocols, regulations, SOPs, and plans.
• Handle local regulatory activities required for clinical trials in South Korea.
• Contribute to SOP development, special projects, and internal/external presentations.

Qualifications & Requirements

Gilead seeks candidates with proven expertise in clinical operations:

• 10+ years of relevant clinical or related experience in life sciences, including multiple years leading studies and project teams.
• Demonstrated leadership in managing teams, coaching, and mentoring colleagues.
• Complete knowledge of full-cycle study management, drug development, and industry best practices.
• Advanced understanding of protocol requirements, ICH guidelines, GCP, and South Korean regulations.
• Strong adaptability, fast learning, and communication skills for clear articulation of complex requirements.

Knowledge & Skills

Success requires significant industry knowledge, flexibility to pivot between projects, and the ability to improve study efficiencies through innovative tools and processes.

Benefits & Perks

Gilead Sciences offers a comprehensive compensation package designed to support your professional and personal well-being:

• Competitive salary estimated at $90,000 - $150,000 USD annually, based on biopharmaceutical sector rates in Seoul with a 5-10% buffer.
• Robust health insurance, retirement plans, and wellness programs.
• Generous paid time off and family leave policies.
• Access to cutting-edge resources and global networks.
• Employee stock purchase plans and performance bonuses.

Career Growth

Gilead invests in your development as a people leader. This role positions you to evolve the company culture, mentor emerging talent, and take on strategic initiatives. With opportunities for advancement in clinical operations, program management, and beyond, Gilead empowers you to fulfill your aspirations. Training programs, leadership coaching, and exposure to international projects accelerate your trajectory in biopharma.

Why Join Gilead

Joining Gilead means contributing to therapies that combat HIV, advance oncology treatments, and address inflammatory diseases, directly impacting millions. In Seoul, you'll work in a dynamic affiliate supporting global trials while navigating local regulations. Gilead's inclusive environment ensures every employee feels valued, developed, and empowered. Be part of a team relentless in pursuit of scientific innovation and global health equity.

Role FAQs

Q: What experience is required?
A: 10+ years in clinical research, with proven study leadership.

Q: Is travel involved?
A: Yes, oversight of study sites and regions may require domestic and international travel.

Q: What therapeutic areas does this cover?
A: All Gilead areas, including HIV, oncology, viral hepatitis, and inflammatory diseases.

Q: How does Gilead support work-life balance?
A: Through flexible policies, wellness resources, and a culture prioritizing employee well-being.

Q: What is the reporting structure?
A: Reports to Clinical Operations leadership, collaborating with program managers and cross-functional teams.