Gilead Sciences-posted 11 days ago
Full-time • Director
Foster City, CA
5,001-10,000 employees

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description The Director, Clinical Development – Inflammation will lead the design, execution, and oversight of clinical trials in support of Gilead’s inflammation portfolio. This individual will play a key role in shaping clinical strategy, collaborating cross-functionally with research, regulatory, safety, and commercial teams to advance innovative therapies that address unmet medical needs in inflammatory diseases.

  • Lead the development and execution of clinical trial protocols for inflammation programs, ensuring scientific rigor and regulatory compliance.
  • Serve as the clinical lead on cross-functional study teams, providing medical and strategic input throughout the clinical development lifecycle.
  • Analyze and interpret clinical trial data; contribute to clinical study reports, regulatory submissions, and publications.
  • Collaborate with external experts, investigators, and regulatory authorities to support program objectives.
  • Contribute to the development of long-term clinical strategies and lifecycle management plans.
  • Mentor and develop junior clinical team members, fostering a culture of scientific excellence and collaboration.
  • Represent Clinical Development in internal governance and external scientific forums.
  • PhD/ Pharm D and 8 years of experience OR MD (or equivalent medical degree) and 4 years’ clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or a related environment.
  • MD or equivalent with board certification or eligibility in a relevant specialty (e.g., rheumatology, immunology, dermatology, or respiratory).
  • Extensive experience in clinical development within the pharmaceutical or biotechnology industry, ideally in inflammation or immunology.
  • Proven track record of leading clinical trials from Phase 1 through Phase 3.
  • Strong understanding of regulatory requirements and clinical trial design.
  • Excellent communication, leadership, and cross-functional collaboration skills.
  • Experience interacting with regulatory agencies and external stakeholders.
  • 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.
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