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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.
Senior Regulatory Affairs Consultant - Regulatory Lead
Job ID R0000035930Join Parexel as a Regulatory Affairs Strategy Lead
Are you a strategic thinker with a passion for navigating the complex world of global regulatory affairs? Do you thrive in cross-functional environments and love transforming regulatory requirements into actionable plans? If so, we’d love to connect.
We’re seeking Regulatory Affairs Strategy Leads who will be the driving force behind regulatory strategy and execution for some of our clients’ most critical development programs. These are high-impact roles where you’ll lead multidisciplinary teams, shape global submission strategies, and serve as a key liaison with Health Authorities.
What You’ll Do
• Lead regulatory strategy for assigned programs from early development through approval
• Coordinate cross-functional regulatory activities (CMC, nonclinical, clinical) to meet key milestones
• Conduct Regulatory Risk Assessments and guide teams through complex decision-making
• Prepare and oversee global submissions, including INDs, CTAs, and marketing applications in eCTD format
• Respond to Health Authority questions during IND/NDA review phases
• Review and approve technical documents across Clinical, Nonclinical, and CMC domains
• Monitor evolving regulations and translate changes into internal SOPs and process improvements
• Collaborate with Regulatory Operations to ensure eCTD compliance and submission readiness
• Support international trials through IMPD preparation and CTA strategy
What You Bring
• B.S. in a scientific discipline (M.S. preferred)
• 7+ years of regulatory experience in pharma or biotech in a similar role
• Proven success designing and executing regulatory strategies for NCEs and biologics
• Deep knowledge of FDA, ICH, and global regulatory frameworks
• Experience with international clinical trials and regulatory documentation
• Strong communication, leadership, and collaboration skills
• Detail-oriented mindset with a proactive approach to problem-solving
• Willingness to travel 15-20%, if needed, in a global work environment
Why You’ll Love Working Here
• Work with both passionate, mission-driven colleagues and client teams
• Influence global development programs that make a difference
• Enjoy flexible work arrangements and a collaborative culture
• Stay ahead of the curve with cutting-edge regulatory tools and training
• Be part of a company that values innovation, integrity, and impact
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