6 days old

GRA Global Regulatory Strategist

Pfizer
Niceville, FL 32578
**GRA Global Regulatory Strategist - Manager**



**Why Patients Need You**

Breakthroughs that change patients' lives... 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're looking to bring medicines to the world faster and we are not willing to compromise on excellence and integrity. Adhering to local and global regulations is essential and the ever-changing regulatory environment requires forward thinking and attention to detail. Your dedication and expertise will help expand and accelerate patient access to Pfizer medicines and vaccines.



**What You Will Achieve**

You will represent Pfizer as an approval liaison in the regulatory affairs team. You will play the critical role of providing strategic product direction to teams while interacting directly/indirectly with regulatory agencies and negotiating with them to expedite approval of pending registrations. Due to your expertise, you will be the regulatory liaison on the project team throughout the product lifecycle and a regulatory representative to marketing or research project teams and government regulatory agencies. Strategies should be in alignment with global/regional positions, commercial goals, and key stakeholders/partner lines.



Your knowledge of regulatory procedures will help in development of submission of product registration, progress reports, supplements/variations and periodic experience reports. You will have an comprehension of the regulatory environment and will communicate priorities to global stakeholders



As a Manager, you provide guidance to operational teams for managing projects. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate concords between different teams.

It is your dedication that will help in making Pfizer ready to achieve new milestones and help patients across the globe.



**How You Will Achieve It**



+ Accountable for ensuring or contributing to Global/Regional Regulatory Strategies and implementation plans (including core labels, risk registers) developed for assigned project/s.

+ Ensures regulatory contributions achieve the objectives in the strategy, achieve agreed standards and minimize resource demands while maximizing overall project delivery time and probability of success and facilitating post filing activities.

+ Partners with project teams and other customer groups (e.g., Country Regulatory Managers, Brand Teams, PGS, etc.) to ensure required regulatory contributions (e.g. briefing documents, line plans, IND, NDA) meet business needs and are provided to the project teams, to agreed time, cost and quality standards.

+ Ensures regulatory plans are monitored, progress/variance conveyed to Senior Management and any risks (from emerging technical data, changing internal objectives or external threats) mitigated.

+ Ensures an aligned regulatory position is reached and communicated for all key issues for assigned project/s, and that these regulatory positions supporting the business are championed and communicated.

+ Works closely with other Regulatory and CMC Product managers within, and across, sites to ensure consistent and appropriate processes, systems, working practices, shared learning's and quality standards.

+ Implements systems, processes and procedures relating to regulatory strategy productivity improvements, ensuring that these facilitate the imparting of information across the relevant lines.

+ Engages in appropriate activities in order to influence the regulatory environment through Agency contacts and Trade Associations as appropriate.

+ Ensures business compliance and implementation of and adherence to Regulatory standards.

+ Develops and maintains constructive working relationship with Health Authority contacts.



**Required Qualifications, Skills and Experience**



+ Bachelor's Degree essential, Master's degree desirable

+ Demonstrable experience of effective delivery in a complex matrix environment

+ Regulatory Knowledge: Knowledge of the regulatory environment and how this impacts regulatory strategy and implementation. Comprehension of regulatory agency philosophy and guidelines. Experience preparing and submitting MAAs, line extensions, NDAs, INDs. Working with and influencing, opinion leaders, external organizations facilitating approval of submissions.

+ In depth knowledge of national/regional regulatory legislation and guidelines.

+ Therapeutic Area Knowledge: Has working knowledge of the therapeutic area, through prior regulatory experience; direct product development and/or academic training.

+ Commercial Awareness: Demonstrated knowledge of global regulatory procedures and requirements. Understanding of regulatory agency philosophy and guidelines. Experience preparing and submitting MAAs and post approval variations.

+ Problem Solving and Analysis: Strong problem identification and solving skills, e.g. risk management planning. Strong logical and analytical skills.

+ Communication skills: Communicates effectively using a variety of mediums appropriate to the setting.

+ Negotiation skills: Can negotiate skillfully in tough situations with both internal and external groups. Can be direct and forceful as well as diplomatic. Gains trust quickly of other parties to the negotiations.

+ Proven examples of delivery across the product's lifecycle with demonstrable contribution in Regulatory Affairs.

+ Proven ability to manage complex regulatory issues.

+ Proven ability to consistently deliver to time, cost and quality standards.

+ Knowledge of pharmaceutical analytics technology, pharmacology, toxicology and medicine

+ Leadership qualities and management skills, team oriented with problem solving skills

+ Strong written and verbal communication and interactive skills



The closing deadline for applications is October 20th.



All applicants must have the relevant authorisation to live and work in the UK / EU as applicable.



\#LI-PFE



Purpose

**Breakthroughs that change patients' lives** ... 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.



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

Categories

Posted: 2020-10-13 Expires: 2020-11-12

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

GRA Global Regulatory Strategist

Pfizer
Niceville, FL 32578

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast