Lavori attuali relativi a Regulatory Affairs Professional, Early Phase Oncology - Milano, Lombardia - Pfizer

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    Milano, Lombardia, Italia Pfizer A tempo pieno

    Job SummaryAs a Senior Associate, Early Phase, Regulatory Affairs, you will represent the EU region for regulatory sciences in relation to our designated early-stage oncology portfolio. You will provide regional strategic expertise as a member of the Global Regulatory Strategic Team (GRST) and lead and implement EU regulatory strategies in agreement with key...

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    Milano, Lombardia, Italia Pfizer A tempo pieno

    {"Job Title": "Senior Associate, Early Phase, Regulatory Affairs", "Job Summary": "As a key member of our Global Regulatory Strategic Team, you will be responsible for representing the EU region in regulatory sciences related to our early-stage oncology portfolio. Your expertise will be crucial in providing regional strategic guidance and implementing EU...

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    Milano, Lombardia, Italia Pfizer A tempo pieno

    {"Job Title": "Senior Associate, Early Phase, Regulatory Affairs", "Job Summary": "We are seeking a highly skilled and experienced Senior Associate to join our Early Phase Regulatory Affairs team in the EU region. As a key member of the Global Regulatory Strategic Team, you will provide regional strategic expertise and lead the implementation of EU...

Regulatory Affairs Professional, Early Phase Oncology

2 mesi fa

Milano, Lombardia, Italia Pfizer A tempo pieno
Job Summary

We are seeking a highly skilled Regulatory Affairs professional to join our team as a Senior Associate, Early Phase Oncology Regulatory Specialist. In this role, you will be responsible for representing the EU region in regulatory sciences related to early-stage oncology portfolio.

Key Responsibilities
  • 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 (from emerging technical data, changing internal objectives or external threats) 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 in order 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 relationship 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
Qualification Skills
  • 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. Equivalent experience, either at a regulatory agency or working on substantive industry-government collaborations, can be considered
  • 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 - Familiarity with factors likely to influence the regulatory environment, including new and emerging guidelines
  • Proven ability in developing and implementing regulatory strategy - Understanding of regulatory agency philosophy and guidelines. Experience preparing and submitting CTAs
  • Communication skills - Ability to communicate complex information and analyses to a variety of scientific audiences in both verbal and written format, including to senior management
  • Presentation skills - Is effective in a variety of formal presentation settings; one-on-one, small and large groups, with peers, direct reports and senior manager
  • 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