[Hiring] Regulatory Strategy Consultant @Parexel

Role Description

We are seeking a Regulatory Strategy Consultant to join our team in a remote capacity. As a Regulatory Strategy Consultant, you will own regulatory strategy across significant programs and portfolios, providing leadership for major regulatory decisions, authority engagement models, and high-impact submissions. This position plays a key role in advancing clinical development through strategic regulatory planning, lifecycle management, and cross-functional collaboration. You'll work with biopharmaceutical partners to shape regulatory pathways, guide long-range development strategies, and drive submissions that bring new treatments to patients.

Responsibilities include:

• Leading regulatory strategy development
• Managing authority engagement
• Overseeing high-impact submissions
• Contributing to long-range development and lifecycle planning

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through strategic regulatory leadership and advancing clinical research. With diverse teams and continuous learning opportunities, the Regulatory Strategy Consultant can explore career paths and expand expertise across therapeutic areas and development phases.

Qualifications

• Strengths in regulatory strategy, strategic planning, and cross-functional leadership
• Extensive experience in clinical development, regulatory affairs, or a highly regulated environment
• The ability to lead across teams, influence stakeholders, and communicate complex regulatory concepts clearly
• A patient-focused mindset and strong attention to regulatory detail and compliance
• Comfort working with regulatory databases, submission management systems, and collaborative platforms

Requirements

• Bachelor's degree in life sciences, pharmacy, medicine, or related field, or equivalent professional experience
• 10+ years of experience in regulatory affairs, clinical development, or related field
• Previous experience with vaccine and/or biologic products is required
• Deep knowledge of ICH-GCP, FDA and international regulatory requirements, and clinical trial processes
• Experience with regulatory tracking systems, electronic submission tools, and clinical development platforms
• Excellent communication, strategic planning, and problem-solving skills with demonstrated leadership ability

Preferred Qualifications

• Advanced degree (M.D., Ph.D., or M.B.A.) or regulatory certification (e.g., RAC) preferred
• Experience in multiple therapeutic areas or development phases
• Familiarity with global regulatory frameworks and international submission strategies
• Fluency in additional languages relevant to regulatory submissions

Benefits

• Health, Vision & Dental Insurance
• Tuition Reimbursement
• Vacation/Holiday/Sick Time
• Flexible Spending & Health Savings Accounts
• Work/Life Balance
• 401(k) with Company match
• Pet Insurance

For a complete list of benefits, please visit www.parexel.com/us-benefits .

Some roles may also be eligible for additional incentives, bonuses, or other compensation programs. Our Talent Acquisition team will provide details on applicable bonus plans or incentive structures for eligible positions.

We offer a comprehensive benefits package to eligible employees, which includes paid time off, a 401(k) match, life insurance, health insurance, and additional benefit offerings in accordance with the terms of our applicable plans.