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Prepare: global clinical regulatory frameworks (IND/CTA, labeling, submissions), CRO–sponsor decision rights, inspection readiness, and how you coach technical teams under accelerated or complex development plans. Bring 1–2 examples of agency interactions and portfolio governance at scale.
Strong fit if you lead clinical regulatory strategy at VP/senior technical level and prefer home-based CRO client work over site-heavy ops. Thin public salary/review data means validate scope, team size, and travel in process.
As Senior / Vice President, Technical – Clinical Regulatory Affairs at Parexel, expect strategy and oversight of regulatory pathways for client trials: guidance strategy, agency-facing quality, cross-functional alignment with clinical and medical teams, and leadership of technical regulatory experts supporting multi-study portfolios—largely remote/home-based collaboration with sponsors and internal delivery teams.
Role family tools in DATA (nursing-adjacent free learning only—not role-specific RA credentials):
The job title includes home-based; the listing also references Phoenix / Maricopa County, Arizona—confirm work-location policy in interview.
Parexel is a CRO that designs and runs clinical trials for pharma and biotech clients to advance drug development.
No. Do not rely on invented ranges; ask compensation band and equity/bonus structure directly.
Website: parexel.com
Parexel is an American contract research organization. It conducts clinical trials on behalf of its pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress.
Public cache only — not an employee review.
Join Parexel as a Senior / Vice President, Technical in Clinical Regulatory Affairs, based in Phoenix, Maricopa County. Lead technical strategy and regulatory excellence for innovative biopharmaceutical clients seeking to bring life-changing therapies to market faster and more effectively. About the Role As a Senior / Vice President, Technical in Clinical Regulatory Affairs at Parexel, you'll partner directly with leading biopharma organizations to shape the regulatory and clinical development strategies that determine how therapies advance through the healthcare landscape. Your expertise will help clients navigate complex regulatory environments, accelerate their timelines, and ultimately bring critical medicines to patients who need them. This is a high-impact leadership position where strategic thinking, deep technical knowledge, and client partnership drive measurable results. What You'll Do Develop and execute comprehensive technical regulatory strategies for clinical and regulatory programs across multiple therapeutic areas Serve as a trusted strategic advisor to senior leadership at biopharma companies, translating complex regulatory pathways into actionable plans Lead technical teams in preparing regulatory submissions, including INDs, NDAs, BLAs, and other critical filings Guide clients through FDA interactions, advisory meetings, and inspection preparation with authority and insight Identify regulatory risks and opportunities early in development, helping clients make informed strategic decisions Collaborate across Parexel's multidisciplinary network to deliver integrated solutions that combine regulatory science, clinical operations, and technical excellence What We're Looking For Extensive experience in clinical regulatory affairs, ideally with prior FDA background or equivalent regulatory agency exposure Deep technical knowledge of drug development processes, regulatory frameworks, and clinical trial design Proven success in a senior leadership or consulting role, managing complex programs and leading teams Strong communication skills with the ability to influence and advise senior executives Strategic mindset combined with attention to scientific and regulatory detail Track record of helping clients accelerate development timelines while maintaining compliance and quality About Parexel Parexel is a leading biopharmaceutical services organization dedicated to supporting the development of innovative therapies that transform patient outcomes. With deep expertise across clinical regulatory affairs, clinical operations, and strategic consulting, Parexel partners with biopharma companies at every stage of the development journey. Our team includes former…
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