Regulatory Affairs Specialist/Regulatory Scientist

Work Schedule Standard (Mon-Fri) Environmental Conditions Office

Job Description
Join Us as a Regulatory Affairs Scientist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have the opportunity to support Regional and/or Global Regulatory Leads in developing and executing regulatory strategies for assigned programs. As a Regulatory Affairs Scientist, you’ll contribute to global and regional programs across development and post-approval maintenance, helping ensure regulatory activities and submissions are aligned with applicable requirements and the overall regulatory strategy. You’ll work collaboratively with Regulatory Leads, subject matter experts and cross-functional teams, contributing to regulatory submissions, Health Authority interactions, risk assessment and regulatory planning while developing your expertise across the global regulatory environment. What You’ll Do: �
� Support the Regulatory Lead in the development and execution of integrated global and/or regional regulatory strategies for assigned programs across development and post-approval maintenance. �
� Contribute to the compilation of regulatory documents for submission to Health Authorities. �
� Support submissions including iPSPs/PIPs, ODDs, Briefing Books, INDs/CTAs, BLA/MAAs and sBLA/Variations. �
� Lead or support collaboration with subject matter experts to provide timely responses to Regulatory Agency queries, ensuring content remains consistent with the agreed regulatory strategy. �
� Develop your understanding of the regulatory environment, competitor intelligence and therapeutic area landscape, and apply these insights to the development of regulatory strategies. �
� Identify and assess regulatory risks associated with specific strategies and contribute to defining appropriate mitigation strategies. �
� Act as a backup or delegate for the Regulatory Lead within project teams or workstreams, helping maintain alignment and a consistent “one regulatory voice.” �
� As applicable, review clinical trial plans, protocols and submission plans for assigned projects to ensure alignment with regulatory requirements. �
� Provide regulatory input and follow-up relating to inspections, audits, litigation support and product complaints. �
� Support the development and continuous improvement of processes related to regulatory submissions. Education and Experience

Requirements:
�
� University degree in a scientific or biomedical field. �
� Minimum 3 years’ experience in a clinical development environment, preferably within Regulatory Affairs. Knowledge, Skills and Abilities: �
� Independent and able to learn quickly. �
� Highly self-motivated with a hands-on approach. �
� Excellent interpersonal skills, with the ability to build effective relationships across a diverse range of stakeholders. �
� Strong leadership and critical-thinking skills, with the ability to work collaboratively to solve problems and make decisions. �
� Sound judgement and the ability to analyse situations and information, making decisions based on facts and evidence. �
� Demonstrated leadership within the context of assigned responsibilities. �
� Able to communicate effectively within teams, with guidance and support from management. �
� Excellent organisational skills and strong attention to detail. �
� Able to prioritise effectively within a fast-paced environment. �
� Proactive and collaborative, with the ability to drive assignments forward across teams. �
� Working knowledge of current global clinical trial regulations. �
� Able to summarise content for focused and maintenance submissions and provide training to others on submissions. �
� Flexible mindset, with the resilience to adapt to changing priorities and regulatory strategies. �
� Able to travel based on business needs.