Associate Program Management Director (Neurology)

Posted 9 Hours Ago
Be an Early Applicant
San Diego, CA, USA
In-Office
174K-238K Annually
Senior level
Healthtech • Biotech • Pharmaceutical
The Role
Lead drug development programs, manage cross-functional teams, develop program strategy, oversee program execution, and ensure alignment with stakeholders.
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 patients with 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:Lead drug development programs of high complexity and priority in partnership with the Program Lead, to develop cross-functional program strategy and long-range plans from pre-clinical development through regulatory approval and commercialization. Drive team alignment in execution of the program plan following strong Project and Program Management theory and practice, including management of stakeholders, schedule, risks/issues, budget, resources and governance processes. Manage program reporting and escalate risks/issues to management as well as highlight team successes to the wider organization. Interact with stakeholders across the organization, including research, CMC, pre-clinical, clinical, regulatory and commercial functions to ensure alignment on program strategy, goals, timelines and resources.

_

Your Contributions (include, but are not limited to):
  • Partner with Program Lead to lead the development and execution of program strategy

  • Establish and maintain functionally integrated program schedules in accordance with established structures to enable accurate project analyses, identification of critical path activities and areas of resource constraint

  • Proactively lead identification and assessment of program risk and response strategies

  • Lead scenario planning efforts to prepare teams for differing outcomes at key milestones

  • Identify and leverage inter-dependencies in short-, mid-, and long-term program plans and advise teams on areas of risk or possibilities to accelerate development

  • Challenge assumptions and provide recommendations to improve processes and outcomes

  • Drive clarity and alignment in complex, ambiguous environments

  • Oversee program team meetings, cross-functional communication and decision making, ensuring alignment with internal functional groups and leadership

  • Develop relationships with key functional stakeholder groups and their leadership across the organization to support the execution of program goals

  • Serve as a Program Management expert resource for the PM group and the broader organization

  • Contribute to the development of the Program Management function through the introduction of new tools and/or processes

  • Contribute to successful execution of Program Management department goals and activities

  • May manage or mentor Program Management staff

  • Other duties as assigned

Requirements:
  • BS/BA degree in Life Sciences discipline AND 10+ years of multi-disciplinary experience in the pharmaceutical/biotechnology industry, including experience with both early and late phase pharmaceutical program management including IND/CTA, BLA/NDA/MAA submissions. Experience managing global drug development efforts OR

  • Master’s degree in Life Sciences discipline AND 8+ years of relevant experience noted above OR

  • PhD in Life Sciences discipline AND 5+ years of relevant experience noted above OR

  • PMP Certification highly desired

  • Strong skills in communications, problem-solving, analytical thinking, influencing

  • Ability to build, coach and lead high-performing cross-functional teams

  • Advanced knowledge of drug development process and inter-dependencies of key functions including research, CMC, non-clinical development, clinical development and operations, regulatory affairs and commercial

  • Experience as a PM leader on early and late phase global drug development programs including: IND/CTA, NDA/BLA/MAA submissions, pediatric development, rare diseases, small molecule and biologic modalities.  Experience in Ph2/3 clinical development, LAI development, neurology, and/or gene therapy preferred.

  • Ability to independently identify and manage project objectives, timelines, budgets, providing formal and informal status updates to stakeholders as needed

  • Ability to manage conflict, drive consensus, challenge assumptions and promote decision-making

  • Experience managing and mentoring direct reports is desired

  • Advanced proficiency in project management practices, tools and methodology, such as Smartsheet or other project management software. PMP designation and Planisware experience desired

#LI-TM1

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.

_

The annual base salary we reasonably expect to pay is $173,900.00-$238,000.00. 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 30% 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

  • BS/BA in Life Sciences and 10+ years experience
  • Master's degree in Life Sciences and 8+ years experience
  • PhD in Life Sciences and 5+ years experience
  • PMP Certification highly desired
  • Advanced knowledge of drug development process
  • Experience managing global drug development efforts
  • Strong skills in communications and problem-solving

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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