Sr IT Project Manager - Commercial | Temporary FT & Onsite

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San Diego, CA, USA
In-Office
Healthtech • Biotech • Pharmaceutical
The Role
Who We Are:

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.

What We Do:

Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)

About the Role:The Senior IT Project Manager leads projects and works with cross functional teams to address business system needs and resolve issues, with key stakeholders across Commercial functions. This role plans and develops the analysis of complex business problems and identifies opportunities to solve them with automated systems, including significant work focused on enhancing and optimizing Salesforce.
It provides technical guidance in evaluating systems and procedures that are cost effective, scalable, and aligned with user requirements. The Senior IT Project Manager plans and executes unit, integration, and acceptance testing and may create specifications to ensure systems meet business needs. The role also serves as a knowledgeable partner to users, offering consultation and support in the effective use of automated systems.

_

Your Contributions (include, but are not limited to):
  • Participates on project teams, may lead small project(s), in the capacity of supporting application implementation, administration, and support

  • Evaluates and recommends process improvements and supports the development of processes required for the successful implementation of key software systems. Provide technical support for the management of data from multiple sources and databases for the eventual submission to multiple regulatory agencies

  • Interacts with Clinical and Regulatory departments on issues relating to electronic submissions

  • Leads evaluating and implementing additional technologies that may improve the overall quality of systems throughout all departments

  • Consults with department representatives to determine requirements for data access, reports, and interfaces

  • Maintains interaction with department managers to ensure successful implementation of data management/interface tools. This will include both regulatory and validation requirements for all Clinical/Regulatory data management projects

  • Other duties as assigned

Requirements:
  • BS/BA degree degree in computer science, IT, or similar field and 4+ years of IT experience working in a pharmaceutical company with exposure to FDA regulations. 5+ years of IT experience with the most recent experience in support of Microsoft applications utilizing the following technologies: MS SQL Server, Oracle, JAVA, Visual Basic, MS Access, MS Project, IIS, Internet Explorer, and Advanced Web technologies such as HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet Database Programming. Experience supporting validated applications for regulatory purposes in a biotech/pharmaceutical company strongly required OR

  • Master’s degree in computer science, IT, or similar field and 2+ years of similar experience noted above

  • PMP certification or working towards a certification is highly desired

  • Understands key business drivers and uses this understanding to accomplish work

  • Has strong understanding of processes, procedures and systems used to accomplish the work and recognizes downstream impact on other functional areas

  • Proficient with tools and processes that support work conducted by functional area

  • Ability to work as part of a team; may train lower levels

  • Possess excellent computer skills

  • Has strong communications, problem-solving, analytical thinking skills

  • Is detail oriented yet can see broader picture for department

  • Ability to meet multiple deadlines, with a high degree of accuracy and efficiency

  • Has strong project management skills

  • Able to communicate technical information and work with all levels within the organization

  • Strong base knowledge of web application technology, electronic document management systems, electronic publishing systems for regulatory filings, and an in depth experience in database technologies and data warehousing/data mining

  • Strong knowledge of the most recent experience in support of Microsoft applications utilizing the following technologies: MS SQL Server, Oracle, JAVA, Visual Basic, MS Access, MS Project, IIS, Internet Explorer, and Advanced Web technologies such as HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet Database Programming

  • Strong knowledge of supporting validated applications for regulatory purposes in a biotech/pharmaceutical company strongly required

Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.

Neurocrine Biosciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Neurocrine Biosciences and has not been reviewed or approved by Neurocrine Biosciences.

  • Strong & Reliable Incentives Total rewards commonly include sizable annual bonuses and RSUs that are characterized as generous. Pay packages are portrayed as robust when combining base, bonus, and equity.
  • Healthcare Strength Medical, dental, and vision coverage begin on the first day with multiple plan options and telehealth access. Health insurance quality is highlighted alongside overall compensation.
  • Parental & Family Support Paid parental and caregiver leave are offered for extended periods in addition to dedicated sick time. Family-building resources and new‑parent support are positioned as part of the core Total Rewards.

Neurocrine Biosciences Insights

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The Company
HQ: San Diego, CA
1,150 Employees
Year Founded: 1992

What We Do

Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company’s diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson’s disease, endometriosis* and uterine fibroids* , as well as clinical programs in multiple therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. Review our Community Guidelines: https://bit.ly/3L8M8hx *in collaboration with AbbVie

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