Vice President, Regulatory Science

Job not on LinkedIn

🔥 15 minutes ago

🌐 United Kingdom, Ireland – Remote

🇬🇧 United Kingdom – Remote 🇮🇪 Ireland – Remote

⏰ Full Time

🔴 Lead

👔 Vice President

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Lead high-impact client engagements as a recognized industry expert • Provide advanced regulatory and scientific consulting services across the product lifecycle • Create opportunities for clients by applying scientific, technical, regulatory, and commercial expertise • Lead teams of subject-matter experts and provide guidance to project team members • Manage project engagements of varying sizes • Prioritize project workloads and deliver project scope and objectives • Resolve project issues and conflicts • Review colleagues’ work for content and quality • Ensure accurate financial management and general project support with the Project Assistant • Present speeches and seminars to industry groups • Author articles for industry magazines, newsletters, book chapters, and other forums • Review colleagues’ thought-leadership activities • Contribute to professional societies, academic groups, industry associations, boards, task forces, and committees • Facilitate improvements to Parexel business processes and development of new consulting models • Adapt and improve consulting methodologies for unique client situations • Represent clients to regulatory agencies • Act as a trusted advisor to clients, including senior and executive management, client boards, and C-suite stakeholders • Identify follow-on business and project-scope opportunities • Build trusted client relationships and contribute to consulting-offering development

🎯 Requirements

• Qualification as a Medical Doctor is required • Therapeutic expertise in General Medicine, Neurology, Immunology/Rheumatology or Endocrinology highly preferred • Minimum 10+ years’ experience with expert-level industry or regulatory knowledge in Clinical Development/Clinical Trial Design, Clinical Strategy, and authoring clinical sections of regulatory applications • Previous experience with a regulatory agency such as the EMA or MHRA as a Senior/Master Medical Review Officer, Team Lead, or related Medical role strongly preferred • Ability to travel up to 20–30% domestically and/or internationally for client and/or Health Authority meetings and thought leadership/conference attendance • Ability to lead high-impact client engagements and provide advanced regulatory and scientific consulting services • Deep technical expertise, client leadership, and industry influence • Ability to present to client boards and provide strategic advice to C-suite and senior/executive management • Ability to develop and implement business solutions addressing client needs • Ability to work individually or within a team environment • Ability to prioritize workloads, resolve issues and conflicts, and mentor junior staff

🏖️ Benefits

• Work/life balance • Work from home • Career opportunities • Opportunity to influence the development strategies of biopharma companies • Industry visibility and thought-leadership opportunities

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