Full-Time

Principal Portfolio and Project Manager

23andMe

23andMe

501-1,000 employees

Personal genomics & biotechnology company

Biotechnology

Senior

San Bruno, CA, USA

Required Skills
Communications
Management
Requirements
  • Ability to work onsite in South San Francisco at least 2 days per week
  • 7+ years' direct experience as a Project or Program Manager in drug discovery and/or drug development
  • Bachelor's degree in a life science discipline. Advanced degree is a strong plus
  • Excellent understanding of pharmaceutical drug discovery and development
  • Successful track record of managing drug discovery/development programs across different therapeutic areas and at different stages of development, from early and late stage research phases through early development
  • Prior experience in managing IND preparation, strategy and timelines required
  • Proven ability to lead cross-functional teams, understand and help teams to prioritize; provide strategic and operational guidance
  • Excellent communication skills, both written and oral. Able to cut to the heart of a problem, find a solution and build consensus around that solution; ability to analyze project progress and metrics, develop project dashboards and other project communication tools
  • Adept facilitation and interpersonal skills with the ability to establish a positive work environment and build important relationships with cross-functional team and other stakeholders
  • Excellent organizational skills. Strong ability to manage a range of complex, high-impact projects simultaneously
  • Ability to influence, negotiate and manage cross-functional teams to support quick project decisions, able to bring alignment out of challenging circumstances, independently set and meet deadlines
  • Proven track record to independently set and meet deadlines and to motivate others to meet deadlines without formal authority and with minimal supervision
  • Ability to proactively identify issues or challenges from a scientific, legal, privacy, or business perspective
  • Ability to work in a dynamic environment with individuals of diverse backgrounds
  • Experience with large molecule development preferred
Responsibilities
  • Partner with scientific and/or clinical project team leaders to manage multiple therapeutic projects to successful and timely decision points from early and late research phases through clinical development
  • Establish and maintain functionally integrated project timelines ensuring accurate inputs are provided by all functional leads
  • Facilitate cross-functional core project team meetings, strategic discussions, and decision making, ensuring cross-functional alignment with team members and other key stakeholders
  • Facilitate cross-functional project communication, prepare clear documentation (meeting minutes, project status reports, and templates for information transparency, ensuring single source of truth for the projects
  • Document, track, and archive project team activities and decisions. Work closely with the scientific/clinical project lead, act as primary contact for project team related information, and develop project updates/reports in a concise manner for upper management and external stakeholders
  • Prepare and track project team budgets including resource requirements and external cost projections. Work with the Finance team to incorporate the project level budgets into the overall budget
  • Manage collaboration projects with industry partners. Work closely with internal and external stakeholders to define deliverables and ensure they are provided within established scope, timeline, and budget
  • Oversee Contract Research Organization operational processes, including assessment and ongoing management of CROs and vendors
  • Provide regular competitive assessments of our current and future Therapeutic programs and specific therapeutic areas
  • Lead and/or help develop key operational initiatives for the Therapeutics team (e.g., budget planning process, time tracking, portfolio management, and communications)

23andMe’s mission is to help people access, understand, and benefit from the human genome. The company has created the world’s largest crowdsourced platform for genetic research and is the only company with multiple FDA authorizations for genetic health risk reports. The company is also in development of discovery programs rooted in a diverse spectrum of human genetics to ultimately deliver reports and results from all spectrums of your DNA.

Company Stage

IPO

Total Funding

$1.2B

Headquarters

Sunnyvale, California

Founded

2006

Growth & Insights
Headcount

6 month growth

0%

1 year growth

-2%

2 year growth

16%

Benefits

Comprehensive health, vision, & dental plans

Family planning, support, & leave for parents

Mental healthcare

Student loan assistance

Volunteer time off

Dog friendly office

INACTIVE