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.
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)
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Partner with Program Lead and Development Team members to manage 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
Assess program risk and support mitigation planning and tracking
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 constructively to improve outcomes and/or provide recommendations to improve processes
Drive clarity and alignment in complex, ambiguous environments
Facilitate and document 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 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
Other duties as assigned
BS/BA degree in Life Sciences discipline and 8+ years of multi-disciplinary experience in the pharmaceutical/biotechnology industry, including experience with both early and late phase pharmaceutical program management including IND/CTA, NDA/MAA submissions. Experience managing global drug development efforts OR
Master’s degree in Life Sciences discipline and 6+ years of similar experience noted above OR
PhD in Life Sciences discipline and 4+ years of similar experience noted above
PMP Certification highly desired
Demonstrated ability to build trust and influence without authority
Track record of challenging team thinking to improve decisions and outcomes
Ability to drive alignment across diverse stakeholders in high-ambiguity environments
Strong bias toward operational efficiency and continuous improvement
Demonstrated self-awareness and leadership presence. Lead by example with accountability, ownership, and transparency.
Sees broader picture and longer-term impact on division/company.
Ability to meet multiple deadlines across a variety of projects/programs.
Demonstrated knowledge of project management practices, tools and methodology
Knowledge of the drug development process and inter-dependencies between key functions including research, CMC, non-clinical development, clinical development and operations, and regulatory affairs
Experience as a PM on early and late phase global drug development programs including some of: IND/CTA, NDA/MAA submissions, pediatric development, rare diseases.
Ability to manage conflict, drive consensus, and promote decision-making
Ability to independently identify and manage project objectives, timelines, budgets, providing formal and informal status updates to stakeholders as needed
Ability to challenge assumptions
Proficiency in Smartsheet, MS Project or other project management software
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 $158,100.00-$216,000.00. 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.