Regulatory Strategy Senior Associate

When our values align theres no limit to what we can achieve.

At Parexel we all share the same goal - to improve the worlds 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 were committed to making a difference.

Please note - This position is part of a talent pool created in anticipation of future opportunities within our Regulatory team. Candidates may be considered for upcoming roles as business needs evolve.

About Parexel
Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22000 employees worldwide we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone anywhere.

We work with focus agility and shared purpose moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking adapt quickly to change and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry-leading innovation With Heart.

About the Role
We are seeking a Regulatory Strategy Senior Associate to join our team in a remote capacity. As a Regulatory Strategy Senior Associate you will support regulatory strategy initiatives that advance new treatments for patients. This position plays a key role in regulatory pathway planning agency engagement support and strategic compliance oversight. Youll collaborate with cross-functional teams follow industry-standard processes and contribute to regulatory strategy from planning through implementation. Responsibilities include developing regulatory pathway recommendations supporting agency engagement planning and identifying key risks and opportunities with opportunities to deepen your expertise and influence regulatory outcomes.

Youll join a fast-paced growth-oriented environment focused on making a meaningful impact through strategic regulatory guidance and product development support. With diverse teams and continuous learning opportunities the Regulatory Strategy Senior Associate can explore career paths and expand skills across regulatory affairs and clinical development.

Key Responsibilities
Develop and recommend regulatory pathways for assigned products studies or markets
Support agency engagement planning and prepare materials for regulatory meetings
Identify key regulatory risks and opportunities to inform development strategy
Align regulatory approaches with development and commercialization objectives
Maintain current knowledge of regulatory requirements and industry guidance
Collaborate with cross-functional teams to ensure regulatory compliance and strategic alignment
Prepare regulatory documentation and submissions as needed
Track regulatory timelines and milestones to support program execution

Candidate Profile
Youll thrive in this role if you bring:
Strengths in regulatory strategy strategic thinking and problem-solving
Experience working in regulatory affairs clinical development or a regulated environment
The ability to collaborate across teams and communicate clearly with internal and external stakeholders
A patient-focused mindset and strong attention to detail
Comfort working with regulatory databases submission tracking systems and standard office tools

Required Qualifications
Bachelors degree in life sciences regulatory affairs pharmacy or related field or equivalent professional experience
4 years of experience in regulatory affairs clinical development or a related field
Previous experience with vaccine and/or biologic products is required
FDA regulation expertise/knowledge is required and experience with other global markets is preferred
Knowledge of ICH-GCP regulatory requirements and clinical trial processes
Experience with regulatory databases or submission tracking systems
Strong communication organization and problem-solving skills

Preferred Qualifications
Advanced degree in regulatory affairs pharmacy or related field
Experience in specific therapeutic areas or development phases
Familiarity with regulatory submission software or electronic tracking systems
Experience supporting FDA or international regulatory submissions

If this job doesnt sound like the next step in your career but perhaps you know of someone whod be a perfect fit send them the link to apply!

We believe in flexibility growth and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research.

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