Regulatory Affairs Senior Manager – Full Time – Uxbridge

  • Contract
  • Uxbridge
  • Country: United Kingdom
  • Address Region: Greater London

Medical/Pharmaceutical/Scientific

Regulatory Affairs Senior Manager required for a 12 month contract role with a leading multinational client based in Uxbridge or Cambridge.

The role
This role will support one or more oncology products from a European regulatory perspective. As a member of the Global Regulatory Team (GRT), you will define the regulatory strategy and support the desired labelling by developing and executing regional regulatory strategies and managing effective agency interactions.

Responsibilities
• Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products within the client’s portfolio in compliance with global filing plans and local regulatory requirements.
• Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements.
• Leads development of regional regulatory documents and meetings in accordance with GRT strategy
• Provides regulatory direction on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, conditional/accelerated approvals , compassionate use and paediatric plan)
• Directs the development of the regional product label by collaborating with the Labelling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent.
• Manages regional label negotiation activities
• With minimal supervision, participate in the development and execution of regional regulatory product strategies, including precedence, risk management and contingency planning
• Consistent with GRT strategy, advise GDT on regulatory implications and requirements related to global clinical development plans and objectives
• Co-ordinates company responses to requests from regulatory authorities, e.g Response to Questions (RTQs)
• Estimate the likelihood of regulatory success based on proposed strategies and discuss with GRT and line Management Develop predictions for expectations and risks associated with outcomes by regulatory agencies
• Ensure regulatory product compliance for product (e.g. IMR, PMCs, paediatric and other agency commitments)
• Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to products.
• Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement.
• Evaluates and communicate impact of relevant regional regulations, guidance, current regulatory environment and competitor labelling
• Act as contact and create relationships with agency staff on specific product assignment
• Document and communicate details and outcomes of regulatory agency interactions to GRT and relevant sr. management
• Manages core regulatory activities to ensure effective regional agency interactions consistent with the Global Regulatory strategy, includes contingency regulatory planning/risk assessment
• Supports communication/collaboration between direct reports who are regional leads and regional head for program issues requiring next level engagement
• Provides managerial leadership & direction to assigned team allowing appropriate prioritization of resources to achieve goals.

Requirements
• Regulatory knowledge in regional legislation Working with policies, procedures and SOPs
• Experience with national legislation and regulations relating to medicinal products
• Understanding of the regional regulatory procedures for CTAs, MAs, post approval changes, extensions and renewals.
• Understanding of drug development Scientific / Technical Excellence
• Strong knowledge of and experience in regional regulatory environment in relevant product area and development stage
• Comprehensive understanding of regulatory activities, touch points and how they affect projects and processes

Interested candidates should submit an updated CV
Please click the link below to apply, call Alba on (phone number removed) or alternatively send an up to date CV alba@peglobal.net
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert.

Salary:

Job Type: Contract

Location: Uxbridge

To apply for this job please visit www.cv-library.co.uk.

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