Sr. Program Manager, Drug Development
$158.1k - $216kNeurocrine Biosciences
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 LinkedIn , X , Facebook and YouTube . (*in collaboration with AbbVie )
About the Role:
Lead drug development teams 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 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 and provide recommendations to improve processes and outcomes
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
May manage other Program Management staff
Other duties as assigned
Requirements:
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
Ability to lead cross-functional teams
Good leadership and mentorship skills
Excellent communications, problem-solving, analytical thinking skills
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 Planisware, Smartsheet, MS Project or other project management software
#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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