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Senior Associate, early phase oncology, Regulatory, Tadworth
Client: [Client Name]
Location: Tadworth, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Reference: d0ba2116a54b
Job Views: 105
Posted: 10.03.2025
Expiry Date: 24.04.2025
Job Description:
Job Summary
* Represent EU region (EU, UK, CH, NZ, AUS) for regulatory sciences in relation to the designated early-stage oncology portfolio
* Provide regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST)
* Lead and implement EU regulatory strategies in agreement with key stakeholders for assigned projects/products and in line with the company goals
* Accountable for timely submissions and approvals in the EU region
* Accountable for ensuring optimal regulatory interactions with Health Authorities, in relation to the designated early-stage oncology portfolio within the EU
Job Responsibilities
* Accountable for ensuring EU contribution to Global Regulatory Strategies and implementation plans (including core labels, risk registers) for assigned early-stage oncology portfolio
* Ensures regulatory contributions achieve the objectives in the strategy, achieve agreed standards, maximizing overall project delivery time and probability of success and facilitating submission activities
* Partners with project teams to ensure required regulatory contributions (CTA, etc.) meet business needs and are provided to the project teams, to agreed time and quality standards
* Ensures regulatory plans are monitored, progress/variance communicated to GRL and Senior Management, and any risks mitigated
* Ensures an aligned EU regulatory position is reached and communicated for all key issues for assigned project/s, and that these regulatory positions supporting the EU business are championed and communicated
* Engages in appropriate activities to influence the EU regulatory environment through GRS-In Country colleagues, Agency contacts, and/or Trade Associations as appropriate
* Ensures business compliance and implementation of and adherence to Regulatory standards
* Develops and maintains, directly or indirectly, constructive working relationships with Health Authority contacts in the EU region
Organizational Relationship
* Reports to early phase Oncology EU lead
* Works with GRS colleagues and relevant project team(s) members (i.e. Clinical and Project Management, Development Operations, Global Regulatory Sciences, Worldwide Risk Management, Worldwide Safety Sciences, Pharmaceutical Sciences, Global Manufacturing Compliance and Legal)
* Partners with EU colleagues, including GRS-in Country colleagues and Medical colleagues, to provide an EU position
* Works directly or indirectly with external contacts in Regulatory Agencies within EU region
* Ensures alignment with GRL and early phase Oncology Global Head
Qualifications
* Scientific Degree. A higher degree may be an advantage but is not essential
* Proven experience in managing national and/or EU regulatory process and registration aspects of the drug development process particularly clinical trials experience at least in one country
* Previous experience as a national and/or EU regulatory liaison for at least one product in different therapeutic areas and in different stages of the product life cycle is highly desirable
* Experience in communicating with major EU regulatory agency(ies) respectively, as well as participating in/leading such interactions, is preferred
* Knowledge of drug development practice rules, regulations and guidelines
* Proven ability in developing and implementing regulatory strategy
* Communication skills - Ability to communicate complex information and analyses to a variety of scientific audiences in both verbal and written format
* Presentation skills - Effective in a variety of formal presentation settings
* Negotiation skills - Can negotiate skillfully in tough situations with both internal and external groups
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.
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!
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms – 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.
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