Director, Clinical Development

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.
 

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Job Description
 

Director, Clinical Development

Job Description

The Director, Clinical Development will play a key role in the design, execution, and evaluation of Phase 1, 2, and 3 clinical trials, providing subject‑matter expertise in pediatric viral infectious diseases. This role will support the development and registration of novel therapies for pediatric viral diseases and will be responsible for a broad range of clinical development activities within the pediatric virology therapeutic area.

The successful candidate will collaborate across multiple functions to support clinical trial start‑up, execution, and close‑out, and will contribute clinical development expertise to data analysis, regulatory submissions, publications, and scientific presentations. The role may serve as Pediatric Development Lead for assigned disease areas, molecules, or products.

As Pediatric Development Lead, you will be responsible for shaping, implementing, and executing the pediatric clinical development strategy, ensuring alignment with overall asset development plans and regulatory expectations.

Essential Functions

• Provide input into, or lead, the development of pediatric development plans for applicable compounds and products

• Serve as a trusted clinical and scientific advisor to cross‑functional teams to support timely and high‑quality clinical development deliverables

• Lead or contribute to clinical trial protocol design, clinical study reports, and responses to health authority inquiries

• Partner closely with Gilead asset development teams to ensure alignment with overall development strategies

• Provide ongoing clinical oversight for clinical trials, including assessment of eligibility criteria, toxicity management, and drug safety surveillance

• Lead or support the preparation and review of regulatory documents, investigator brochures, and development plans

• Coordinate the collection and synthesis of ongoing clinical data for internal analysis and review

• Oversee the preparation and/or review of data listings, summary tables, study reports, and scientific presentations

• Present scientific and clinical data at investigator meetings and international scientific conferences

• Ensure compliance with applicable regulatory requirements, industry standards of Good Clinical Practice (GCP), and Gilead SOPs

Knowledge, Experience & Skills

• MD or equivalent medical degree, PharmD, or PhD in a clinical and/or scientific discipline, or equivalent combination of education, training, and experience

• Experience in pediatric medicine and/or pediatric drug development is highly desirable, with direct hands‑on pediatric development experience strongly preferred

• Familiarity with virology, including HIV, viral hepatitis, COVID‑19, or related viral infectious diseases, is preferred

• Pharmaceutical or biotechnology industry experience in clinical development is preferred

• Demonstrated experience working on cross‑functional, matrixed project and program teams within life sciences, healthcare, academia, or consulting environments

• Strong verbal, written, and interpersonal communication skills

• Proven ability to manage complex clinical development projects, balancing multiple priorities and deliverables through influence and leadership

• Strong analytical and problem‑solving capabilities, demonstrated through professional experience and/or academic research

• Thorough understanding of global pharmaceutical regulatory requirements and their impact on the design and execution of clinical trials

• Willingness to travel as required

Equal Employment Opportunity (EEO)

It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual’s gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.

For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.