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

Pfizer
Niceville, FL 32578
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**Hub Submission Manager, EME / EU (multiple roles each region)**



Breakthroughs that change patients' lives... At Pfizer we are apatient 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:**



+ 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.

+ Operate as Subject Matter Expert in dossier types and/or processes with responsibility for training and mentoring fellow colleagues

+ Escalates, informs, and resolves any issues that may impact submission builds or the logistics of global submission delivery to regional partners or Health Authorities.

+ Promotes the use of Document Management and Archival systems and standard document authoring and publishing processes, partnering with supplier groups as necessary in order to produce timely delivery of submission/archive ready components.

+ Functions as a change agent that can exhibit regulatory knowledge and awareness, technical proficiency, sound judgment and a professional demeanour

+ Engages Submission leaders, business suppliers and other key regional representatives as appropriate, to agree on process and activities for opportunistic re-use of submission documentation for multiple national markets.

+ Directs the interpretation of regulatory guidelines to produce business requirements and ensure that those requirements are implemented where appropriate at local level.

+ Manages own time to meet objectives; forecasts and plans resource requirements (people, financial and technology) for projects across Department Provides guidance to and directs moderately complex submission and process improvement projects, making decisions independently

+ Considered a technical resource within the group

+ Regularly takes informal leadership role during Work Team meetings to facilitate agreements and move the group toward its goals



**Technical Skill Requirements:**



+ 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

+ Formal training in technical tools

+ Knowledge of drug development process

+ Ability to work on multiple highly complex projects simultaneously.

+ Strong knowledge of the drug development process, regulatory affairs, and submissions management.

+ In depth understanding of systems and electronic technologies used to support submission and planning activities, as well as demonstrated experiences in process development and new technology implementation.

+ Ability to operate seamlessly and influence/mentor direct and indirect reports, as well as across organizations.



**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.



Closing deadline for applications is June 26th.



All applicants must have the relevant authorisation to live and work in the UK.



Purpose



**Breakthroughs that change patients' lives** ... At Pfizer we are apatient 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.



Digital Transformation Strategy



One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.



Flexibility



We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self.Let's start the conversation!



Equal Employment Opportunity



We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer iscommitted to celebratingthis,in all itsforms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.



Regulatory Affairs
Posted: 2021-06-11 Expires: 2021-07-12
Sponsored by:
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Hub Submission Manager, EME / EU (multiple roles each region)

Pfizer
Niceville, FL 32578

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