Hub Submission Manager, EME / EU (multiple roles each region)

Recruiter
Pfizer
Location
Tadworth
Salary
Negotiable
Posted
31 Mar 2021
Closes
14 Apr 2021
Ref
4808521
Hours
Full Time
Contract Type
Permanent

At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives. We are currently recruitment for multiple Hub Submission Manager (HSM) roles. Each HSM role will be dedicated to either EU or EME region.

Position Purpose

The Hub Submission Manager is accountable for operational management of regional and/or national regulatory dossiers to designated Health Authorities (HA's) Based within GRA Submission Management, this role sits within a team working to tight, business critical deadlines within a highly regulated environment. Primary focus is on allocated region/ countries, with additional responsibility to support other locations through utilization of global tools. On behalf of Global Regulatory Affairs (GRA), guide and manage logistical and technical aspects, ensuring development and delivery of X-regional, regional and/or national regulatory dossiers - initial application and subsequent lifecycle updates (compliance and maintenance). Execute, through use of standards and tools, designated operational tasks e.g. submission planning, document receipt, translation management, technical build and submittal to HA or via the applicable Pfizer country office, conforming to regulatory submission milestones and applicable regulatory obligations. Given the scope of international work, critical features of this role are the ability to successfully interface with multiple cultures and, to recognize and exploit opportunities to use scale, cloning and repurposing dossiers for worldwide markets where feasible.

Primary Responsibilities (include but not limited to):

  • Drive submission coordination activities for assigned products and/or regulatory procedures as appropriate. Partnering with product teams and/or third-party partners, the incumbent will be responsible for project management of activities, in support of regional and national regulatory submissions component build and delivery.
  • Delivering project specific Pfizer electronic and paper regulatory submissions. Including co-ordination and execution of solutions that meet unique requirements of each submission and national market, management of product delivery to regulatory agencies and ensuring subsequent archival.
  • Ongoing liaison with Project Team and country representatives to ensure paper and electronic submission requirements, translation requirements and timelines are mutually understood and in line with corporate standards and deadlines for dossier delivery to regional and national markets.
  • Actively participate in the definition, investigation and implementation of national, regional and global process efficiencies for paper and electronic submission execution, including the evaluation of current processes.
  • Completion of assignments and tasks within a specific task group/project associated with electronic and paper submissions.
  • Help interpret regulatory guidelines to produce business requirements and ensure that those requirements are implemented where appropriate at local level.
  • Contribute to effective forecasting and management of project specific resources utilizing flexible resourcing, and global load sharing as normal business practice.
  • Adhere to the appropriate use of technical tools, through use of working practices and QC/QA regimes, such that regulatory and internal compliance is preserved.

 

Required Skills, Experience and Qualifications:

  • B.S./B.Sc is in Pharmacy, Life Sciences, Business or Information Technology (desirable); equivalent relevant professional experience could be considered.
  • Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards.
  • Multi-lingual skills desirable.
  • Familiarity with pharmaceutical organizational structures, systems, and culture is preferred.
  • Demonstrated coordination of activities in a highly regulated environment
  • Proven aptitude in project management and logistics
  • Demonstration of experience working in a stimulating customer service environment
  • Proven experience managing or delivering through others in a team environment
  • Demonstrated attention to detail
  • Relevant experience in electronic submissions build within the Pharmaceutical Industry
  • Understanding of applicable filing regulatory guidelines and fluency regarding order and presentation of regional and national regulatory dossiers
  • Ability to work on multiple highly complex projects simultaneously.
  • Strong knowledge of the drug development process, regulatory affairs, and submissions management.

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