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The Regulatory Project Manager (RPM) is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables. The RPM contributes to regulatory submission strategy, identifying submission risks and ...

Job Description

The Regulatory Project Manager (RPM) is a regulatory specialist with project management capabilities responsible for leading the end-to-end planning, coordination, and execution of assigned deliverables. The RPM contributes to regulatory submission strategy, identifying submission risks and opportunities, while leading simple through more complex regulatory applications and managing procedures through approval. The RPM provides regulatory expertise and guidance on procedural and documentation requirements to GRET, GRST and cross-functional teams working flexibly within and across regions to ensure the delivery of business objectives. 

Looking for candidate with : 
Operational Submission experience 
Project Management Experience 
Regulatory Affairs 
Pharma background 
Can navigate MS project and manage meetings 
SBLA 

Accountabilities/Responsibilities: 
• Understand the regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions. 
• Provide regulatory input on procedural and documentation requirements as defined by Health Authorities for assigned deliverable(s) including: 
   o Submission delivery strategy of all dossiers and all application types per market and /or region. 
   o Review of documents (e.g. response documents, study protocols, PSRs, etc.). 
   o Analysis of regulatory procedures and special designations used during development, authorizations and extension of the product. 
• Use and share best practices, when handling various applications and procedures during interactions with health authorities and in day-to-day work, while operating in a highly dynamic environment. 
• Lead and/or contribute to the planning, preparation (including authoring where relevant) and delivery of simple and with experience, increasingly more complex submissions throughout the product’s life cycle from either a global and/or regional perspective. 
• Develop, execute and maintain submission delivery plans, submission content plans, and proactively provide status updates to designated stakeholders. 
• Coordinate the input, maintenance and revision in the OPAL project plans for assigned projects, and highlight unforeseen changes in resource demand in a timely manner to Lead RPM and line manager. 
• Identify regulatory risks and propose mitigations to Lead RPM and cross functional teams. 
• Support operational and compliance activities for assigned deliverables, including generating work requests and submission content plans, submission tracking, TMF, and document management utilizing the support and input of GRO, MCs, CROs and/or alliance partners where relevant. 
• Provide coaching, mentoring and knowledge sharing within the RPM skill group. 
• Contribute to process improvement. 

Minimum Requirements –Education and Experience 
• Relevant University Degree in Science or related discipline 
• Regulatory experience within the biopharmaceutical industry, or at a health authority, or other relevant experience 
• General knowledge of drug development 
• Strong project management skills 
• Leadership skills, including experience leading multi-disciplinary project teams 

Internal and External Contacts/Customers 
• Global Regulatory Leads (GRLs) 
• Regional Leads (eg, US, EU international RADs) 
• Lead RPM 
• Other GRAPSQA skill groups, eg, GRO, GLG, Reg CMC, CMC RC, PS 
• Other Science Unit functions within the IMED and GMED 
• Operations (CMC post approval) 
• Marketing Companies 
• Health Authorities 
• External collaboration partners