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Sr Director, Clinical Development LIVER (MD)

Gilead Sciences, Inc. • Foster City, CA, United States • $200k - $250k / year • 1m ago

Sr Director, Clinical Development LIVER (MD)

Locations: United States - California - Foster City, United States - Washington - Seattle

Time Type: Full time

Posted on: Vor mehr als 30 Tagen

Job Requisition ID: R0040067

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.

POSITION OVERVIEW:

You may act as a Clinical Development Lead and Physician Responsible on clinical trial programs in the Inflammation and Fibrosis therapeutic area. Clinical development activities include molecules/products targeting primary biliary cholangitis (PBC), other cholangiopathies, and metabolic dysfunction-associated steatohepatitis (MASH). The ideal candidate would have a strong clinical background in hepatology, along with experience in drug development. As Clinical Development Lead, you will be accountable for the design, conduct, evaluation, close-out, and reporting of clinical trials for the assigned molecules/products.

EXAMPLE RESPONSIBILITIES:

Integrates with a team providing matrix leadership that ensures execution of innovative, highly proficient, and feasible strategies for drug development specific to a portfolio of therapeutics targeting inflammatory & fibrotic diseases.
Works closely with cross-functional leaders and teams to develop, implement, and oversee the clinical development strategy for the assigned molecules/products.
Leads or oversees and directs clinical trial protocol design and clinical study reporting for assigned molecules/products.
Provides or oversees ongoing medical monitoring for clinical trials, including assessment of eligibility criteria, toxicity management, and drug safety surveillance.
May assist in the clinical evaluation of business development opportunities.
Adheres to regulatory requirements of study conduct and industry standards of Good Clinical Practice as well as Gilead SOPs.

REQUIREMENTS:

Minimum Education & Experience:

MD or equivalent with 6+ years’ clinical, scientific, and/or drug development experience in the biopharma industry.
Board certification in hepatology and/or gastroenterology is preferred.
Multiple years’ experience leading high-complexity cross-functional drug development strategies and plans.
Demonstrated excellence leading large and complex teams in life sciences, healthcare, consulting, or academia.

Knowledge & Other Requirements:

Expert-level knowledge of drug development with a proven track record in setting drug development strategies.
Strong communication and organizational skills.
Ability to think analytically and strategically to formulate, develop, and execute clinical plans.

The salary range for this position is: $295,290.00 - $382,140.00. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives, paid time off, and a benefits package.

For additional benefits information, visit: Gilead Benefits

As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination.

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