Sr Manager, Biostatistics

Gilead Sciences•Foster City, CA

3d•$169,320 - $219,120

About The Position

The Sr Manager, Biostatistics collaborates with statistical programmers, biostatisticians, clinical research associates, clinical data managers, and other clinical, global drug safety, regulatory, and project management staff to deliver statistical data analysis and reporting on project timelines. The role directs internal and external teams across multifunctional projects or functional areas, leads efforts to gather, organize, and analyze data from sources such as virology, case report forms, and patient tracking, and works with management and Human Resources to address short-term staffing needs. The position oversees and contributes to technical and operational statistical activities for a group of clinical trials for a compound or indication, or equivalent, by managing internal and external resources. It also provides senior-level review of technical documents, advises colleagues to support decision-making and problem-solving, addresses client obstacles, and builds effective teams with a clear sense of direction. The role calls for strong verbal, written, and interpersonal communication; the ability to evaluate issues from multiple perspectives; and the judgment to identify critical functions and support priorities within the functional area. The stated U.S. salary range is $169,320 to $219,120. The position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary by role), paid time off, and company-sponsored medical, dental, vision, and life insurance plans.

Requirements

Excellent verbal and written communication skills.
Excellent interpersonal skills.
Ability to examine issues from various perspectives and apply appropriate concepts to address situations.
Ability to identify the functions most critical to company success and support priorities within the functional area.

Responsibilities

Collaborate with statistical programmers, biostatisticians, clinical research associates, clinical data managers, and other clinical, global drug safety, regulatory, and project management staff to meet deliverables and timelines for statistical data analysis and reporting.
Direct internal and external teams across multifunctional projects or functional areas.
Lead initiatives to gather, organize, and analyze data from sources such as virology, case report forms, and patient tracking.
Work with management and Human Resources to satisfy short-term staffing needs.
Oversee and contribute to technical and operational statistical activities for a group of clinical trials for a compound or indication, or equivalent, by managing internal and external resources.
Provide senior-level review of technical documents.
Advise colleagues to support better decisions and resolve problems.
Address client obstacles and difficulties to meet goals.
Build effective teams and create a clear sense of direction.