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Roivant Sciences // biomedical research
 
Roivant Sciences, 151 West 42nd Street, 15th Floor, New York City 10036    Posted: Thursday, February 11, 2021
 
   
 
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JOB DETAILS
 

Summary:

Roivant is seeking a knowledgeable cross-functional drug development program manager with strong project leadership skills that enjoys working in a high energy, entrepreneurial environment. Manage development projects from initiation through product launch by establishing & leading cross-functional product development teams. Lead the coordination of due diligence in-licensing activities for the R&D team. The program manager is the focal point for senior management program communication & will interact with, & influence, senior internal & external stakeholders. The Program Manager will develop & manage timelines to ensure project deliverables are being met on time & within budget. This is a highly-visible & critical role that offers a chance to make significant contributions to various research & development programs in several therapeutic areas.

Essential Duties & Responsibilities

  • Drive implementation by establishing development strategy, schedules, & budgets.
  • Resolves project issues by working with team members, project customers, & others as appropriate
  • Responsible for identifying critical project issues & risks, & timely communication to senior leadership
  • Excellent communication & time management skills to meet expectations of all stakeholders
  • Maintains direct interaction with R&D, quality, regulatory, operations, & manufacturing organizations in the Company & with external partners
  • Lead & manage the projects effectively & to ensure they are delivered on time, on budget, & to agreed quality standards by generating high quality global strategic integrated project plans
  • Managing standards, procedures & practices of record-keeping

Requirements/Qualifications:

  • BS/BA degree in the health sciences & have a demonstrated track record of success
  • Experience in pharmaceutical drug development is required
  • Preclinical & Phase I/II/III/IV expertise, & 5+ years of experience in managing and/or leading cross-functional drug development teams
  • Drug development knowledge with advanced understanding of other functions including, but not limited to: Research, Pre-Clinical, Clinical, Manufacturing & Operations, Commercial, Regulatory, Safety & Payer
  • Knowledge of applicable quality & regulatory standards requirements for pharmaceutical industry
  • Experience project managing the in-licensing due diligence process is a plus
  • Understanding of Good Manufacturing Practices & Product Development Process requirements
  • Demonstrated leadership skills in collaborating & influencing cross-functionally
  • Strong organizational & interpersonal skills
  • Strong planning & execution skill Experience using MS Project or equivalent is a must
  • Strong written & oral communication skills
  • Critical thinking/problem-solving skills
  • Demonstrated competencies in all aspects of project management
  • PMP certification desired
 
 
 
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