Orion Group Sciences are looking for a Regulatory Affairs Manager for our multinational pharmaceutical client based in the Middlesex area on an initial 12-month contract with the potential to extend.
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
Main Responsibilities of the role
This role is responsible for:
Advising the GRT on regional considerations in developing strategy Ensuring the regional needs are well defined and implemented in collaboration with relevant regional stakeholders May manage one or more regional leads or support roles Strategy and Execution Plans and manages regulatory submissions (e.g. clinical trial and marketing applications) for products within companies 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) Communicates regulatory strategies as appropriate such that expectations are understood.
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) Collaboration Share regulatory information and implications with the GRT colleagues on an ongoing basis and provide advice on regional considerations Communicate and ensure alignment of regional management before GRT strategy decisions Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Maintains an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to 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’s, current regulatory environment and competitor labelling Health Authority Interactions 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 Management 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 goalsDesired Experience and Background of the successful candidate
Knowledge and Skills 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 Ability to resolve conflicts and develop a course of action leading to a beneficial outcome Cultural awareness and sensitivity to achieve results across both
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For more information on this role, call Kate O’ Sullivan on +44 (0) (phone number removed) or email (url removed) for a completely confidential chat about this role and other opportunities using the reference number: (phone number removed)
Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Job Type: Contract
Location: Uxbridge, London
To apply for this job please visit www.cv-library.co.uk.