When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel is seeking a Regulatory Affairs Strategist (Regulatory Affairs Consultant) with extensive experience in EU, US, and ROW markets. As a Regulatory Strategist, you will play a crucial role in providing regulatory representation in cross-functional teams, developing regulatory strategies, and advising on regulatory expectations, requirements, and timelines. This is a client dedicated project. This role can be home or office based in various European locations. Responsibilities: Develop and implement regulatory strategies for global submissions in accordance with applicable regulations. Prepare, maintain, and coordinate regulatory submissions including INDs, CTAs, NDAs, MAAs, MATs, and LCM, ensuring compliance with regulatory guidelines. Identify regulatory scientific data needs and resolve regulatory issues. Serve as the primary Health Authority contact for routine communications related to submissions. Assist in preparing for and participating in regulatory authority meetings, inspections, and response to agency questions. Collaborate cross-functionally to ensure regulatory compliance and support strategic initiatives. Qualifications: Bachelor's degree in a scientific discipline and a minimum of 5 years of regulatory experience; or Master's degree with a minimum of 3 years of experience. Solid knowledge and understanding of the drug development process and regulatory requirements for EU, US, and ROW. Experience in the preparation and submission of documentation to support regulatory submissions. Excellent oral and written communication skills. Strong technical and analytical skills to independently identify and solve problems. Proven ability to manage multiple projects, identify and resolve regulatory issues. Strong organizational skills to maintain a high level of productivity, innovation, and priority-setting. Experience working cross-functionally on broad and strategic initiatives. Ability to work under pressure, meet time-sensitive deadlines, while maintaining a high level of quality. Fluent in English, written and spoken Join our dynamic team at Parexel and contribute to the development of innovative therapies that have the potential to improve patients' lives worldwide. Apply now and take the next step in your regulatory career! Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.