Senior IT Program Manager

Posted Yesterday
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San Diego, CA, USA
In-Office
103K-141K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Leads or supports moderately complex IT initiatives from initiation through stabilization, managing scope, schedules, budgets, risks, issues, dependencies, compliance, validation, governance, and stakeholder communications. Develops project plans, portfolio and steering committee reports, and value-realization measures. Partners with IT and business stakeholders on platform roadmaps, demand intake, and commercial operations initiatives, particularly within clinical and regulatory systems. Requires pharmaceutical IT experience, FDA-regulated validated applications expertise, strong technical knowledge, and project management skills.
Summary Generated by Built In
Who We Are:

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, 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 more than 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 LinkedInX, Facebook and YouTube. (*in collaboration with AbbVie)

About the Role:Operates within the Value Management Office Delivery Project & Program Management organization and supports the disciplined execution of moderately complex IT initiatives.
Supports or may lead cross-functional technology projects from initiation through stabilization under broad supervision, helping ensure delivery against defined scope, schedule, budget, quality, compliance, and business outcome expectations. Partners closely with IT and business stakeholders to support effective governance, predictable execution, and alignment with established enterprise strategies and goals.
Execution- and delivery-focused, emphasizing governance, risk management, stakeholder coordination, and transparent reporting to support measurable business value.

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Your Contributions (include, but are not limited to):
  • Support or lead the execution of moderately complex IT initiatives under broad supervision

  • Contribute to the delivery and measurement of defined business outcomes

  • Translate defined objectives into detailed project plans, milestones, and deliverables

  • Support adherence to regulatory, validation, and compliance requirements throughout project execution

  • Support predictable delivery through disciplined task, risk, issue, dependency, and scope management

  • Prepare and maintain consistent project, portfolio, and steering committee reporting

  • Partner with IT and business stakeholders to coordinate initiative delivery with established platform roadmaps and technology plans

  • Ensure regulatory, validation, and compliance requirements are embedded into project execution (particularly in Clinical and Regulatory systems environments)

  • Support the tracking and reporting of defined value-realization measures

  • Works independently to lead initiatives within the commercial organization

  • Partners with IT Business Partners to manage the demand intake process

Requirements:
  • BS/BA degree in computer science, IT, or similar field

    and 4+ years of IT experience working in a pharmaceutical company with exposure to FDA regulations. Experience supporting validated applications for regulatory purposes in a biotech/pharmaceutical company required OR

  • BS/BA degree in computer science, IT, or similar field

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

  • 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 required

  • 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

  • Possess excellent computer skills

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

  • Detail oriented yet can see broader picture for the department

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

  • Has strong project management skills

  • Knowledge of Commercial Operations, including field/product support and Omnichannel activities, and the business processes required to act as an effective commercial project manager

#LI-CL1

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.

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The annual base salary we reasonably expect to pay is $103,300.00-$141,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 20% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.

Skills Required

  • Bachelor’s degree in computer science, information technology, or a related field, plus 4 or more years of IT experience in a pharmaceutical company with FDA regulation exposure and validated application support experience; alternatively, a master’s degree in a related field plus 2 or more years of similar experience.
  • Experience supporting validated applications for regulatory purposes in a biotechnology or pharmaceutical company.
  • Knowledge of web application technology, electronic document management systems, electronic publishing systems for regulatory filings, database technologies, data warehousing, and data mining.
  • Experience with MS SQL Server, Oracle, Java, Visual Basic, MS Access, MS Project, IIS, Internet Explorer, HTML, XML, SGML, Dynamic HTML, JavaScript, VBScript, and Internet database programming.
  • Ability to communicate technical information and work effectively with all organizational levels.
  • Understanding of business drivers, business processes, procedures, systems, and downstream impacts across functional areas.
  • Proficiency with functional-area tools and processes, strong computer skills, and ability to work as part of a team.
  • Strong communication, problem-solving, analytical thinking, attention to detail, and ability to manage multiple deadlines accurately and efficiently.
  • Strong project management skills.
  • Knowledge of commercial operations, including field or product support, omnichannel activities, and related business processes.

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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