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Regulatory Global Submission Manager Poznań

Termin ważności:
2020-09-25 - 2020-11-30
Województwo / region:
Poznan, wielkopolskie
Firma:
ukryte

For one of our clients - a multinational pharmaceutical company we are looking for:

Regulatory Global Submission Manager

Responsibilities:

  • Accountable to Global Regulatory Lead and Global Regulatory Affairs staff for the project management of major submissions.
  • Provides guidance to project teams and client groups on submission related processes and content and format requirements for key markets.
  • Through collaboration with contributing functional lines, creates and maintains a Global Submission Plan that captures detailed list of dossier content, key activities and timelines associated with delivery of that content, target governance board review time frames, and credible dispatch and Health Authority approval dates for key markets.
  • To ensure company’s competitiveness in drug development, work with teams to identify ways to optimize and accelerate bringing products in our late-stage pipeline to market, focusing on key activities and processes from last subject last visit (LSLV) to submission and approval.
  • Leads submission planning discussions, ensuring team is aware of upcoming deliverables, aligned on roles and responsibilities, understands the inter-dependencies between submission activities and components, and that any issues, risks, or impact due to changes in strategy and/or timelines are assessed quickly throughout the submission process.
  • Performs scenario planning when multiple regulatory strategies are being considered.
  • Provides various visuals, reports, scorecards, etc. to facilitate awareness of key milestones, closely monitors critical path activities, and ensures transparency of submission status to stakeholders.
  • Works closely with data generating groups to monitor progress and ensure team is on-track to delivery according to plan. When potential issues and delays are identified, works to expeditiously find solutions in order to keep the team progressing toward the target submission time frame.
  • Responsible for understanding, adhering to, and advising others on global Regulatory Authority regulations and guidance associated with electronic submissions, which differ across regions and Regulatory Authorities.
  • Facilitate post-submission after action reviews (AARs) to identify key learnings and best practices which are then used to refine and improve submission processes.
Qualifications:
  • Education – preferred degree in a biological, health care, or life science discipline.
  • Project management experience in the pharmaceutical industry, preferred in regulatory environment.
  • Understanding of the pharmaceutical drug and vaccine development environment, and R&D processes and objectives.
  • General knowledge of Regulatory Affairs responsibilities from pre-IND through Phases I-IV.
  • Proficiency with Microsoft Project and/or other project management tools will be an asset.
  • Ability to interpret regulations and gain consensus on a way forward in an environment where there may be more than one way of achieving a successful outcome.
  • Effectively lead multidisciplinary team meetings and drive discussions regarding submission content, timelines, resource allocation, risk management, etc.
  • Ability to proactively identify and mitigate risks and potential bottlenecks and effectively interact with stakeholders to ensure transparency of submission progress/status.
  • Excellent organizational skills, attention to detail and commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines.
  • Ability to lead in a matrix environment and ensure delivery of objectives across cross-functional teams.
We offer:
  • Important and interesting job in one of the leading global healthcare companies.
  • An opportunity to play a key role in bringing new medicines and vaccines to patients.
  • A position that liaises with various functional areas and culminates years of work into a marketing application that is submitted around the world.
  • Possibility to work with engaged and enthusiastic people from various locations.
  • Training on the newest project portfolio management software solutions and content management platforms.
  • Possibilities of development within the role and company’s structure.
  • Benefits (e.g. private medical healthcare, life insurance, sports card, pension plan, flexible working hours, home office).
  • Corporate culture based on our values: patient focus, integrity, respect and transparency.

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