Gilead Sciences

Gilead Sciences

VP, NonClinical Safety and Pathobiology

United States - California - Foster City · Vp

Sponsorship not specifiedDetected 74 days ago
Clinical TrialsPharmacologyResearchAnimal ModelsLeadershipCollaborationCritical ThinkingOrganizational Skills

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odds of building a lasting career here

38Risky
Cap-exempt (no lottery)0
Sponsors this role85
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 70 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 71%

Of 38 labor certifications old enough to have been used, 11 expired without the employer filing the next step. Median time from filing to decision: 482 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Files H-1B transfers

34 transfer filings in the last year, covering 34 workers. Median labor-condition decision: 7 days. An employer that already files transfers is one that can take over an existing H-1B.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • At Gilead, we're creating a healthier world for all people.
  • 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.

Responsibilities

  • Nonclinical Safety and Pathobiology (NSP) group is responsible for design, implementation, oversight and analysis of nonclinical programs to support drug development candidates from research to registration.
  • NSP is responsible for ensuring global compliance with worldwide regulations governing the conduct of Gilead's nonclinical studies in support of global clinical trials, registration, and new drug approvals.
  • Manages and mentors a group of Ph.D. level toxicologists and pathologists to ensure NSP continues to develop and implement cutting edge scientific technologies and drug development strategies.
  • Prepares and reviews regulatory documents including INDs/IMPDs, Investigator Brochures and NDAs/MAAs.
  • Join Gilead and help create possible, together.

Requirements

  • Knowledge of global regulatory guidelines associated with quality and compliance in the conduct of nonclinical safety studies is required.
  • Should have at least 20 years of experience in research or development in a pharmaceutical company or contract research organization.

Compensation

  • However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have

Benefits

  • 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.

Company info

  • 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.

This listing is sourced directly from Gilead Sciences's careers page and normalized into a canonical job model.