Neurocrine Biosciences, Inc.

Sr. Program Manager, Drug Development

Neurocrine Biosciences, Inc.$158K — $216K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA in Life Sciences with 8+ years in pharmaceutical/biotech; or Master's with 6+ years; or PhD with 4+ years
  • PMP Certification preferred
  • Proven ability to lead cross-functional teams effectively
  • Strong communication, problem-solving, and analytical skills
  • In-depth knowledge of drug development processes and methodologies

Responsibilities

  • Partner with Program Lead to shape and execute program strategy
  • Develop and maintain integrated program schedules ensuring project timelines
  • Identify program risks and manage mitigation strategies
  • Lead scenario planning for key project milestones
  • Facilitate cross-functional communication to ensure project alignment
  • Build and nurture relationships with key stakeholders
  • Contribute to enhancing Program Management practices with new tools

Benefits

  • Retirement savings plan with company match
  • Paid vacation, holiday, and personal days
  • Paid caregiver/parental and medical leave
  • Comprehensive health benefits including medical, dental, and vision coverage
Full Job Description
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

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.

About Neurocrine Biosciences, Inc.

Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company dedicated to discovering, developing and delivering life-changing treatments for people with serious, challenging and under-addressed neurological, endocrine and psychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson's disease, endometriosis* and uterine fibroids*, with three pivotal and five early-stage clinical programs in multiple therapeutic areas. (*in collaboration with AbbVie)
Learn more about Neurocrine Biosciences, Inc.
Size
900 employees
Market Cap
$11.6 billion
Industry
Net Income
$407.3 million
5 Year Trend
+137.5%
Revenue
$1 billion
NASDAQ

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