Regulatory Affairs Lead

Join Qps

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.

Team members enjoy challenging and rewarding work and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.

If this sounds like your ideal work environment, then we would love to speak with you, so apply today!

The job

As a Regulatory Affairs Lead with QPS (a full-service, global Contract Research Organization), you will lead regulatory strategies and submission activities for sponsor clients across multiple therapeutic areas, with a focus on U.S. FDA submissions. You will oversee regulatory deliverables, collaborating with internal teams and sponsor stakeholders to ensure high-quality, compliant submissions that meet all applicable health authority requirements.

Key Responsibilities

• Serve as the primary regulatory lead on sponsor projects, advising on and implementing submission strategies for INDs, NDAs, amendments, and other FDA-regulated filings.
• Manage and coordinate the preparation, review, and timely submission of regulatory documents to the FDA and other U.S. health authorities.
• Participate in regulatory authority meetings (e.g., Pre-IND, Type B / C) and assist sponsors with briefing package development and logistical planning.
• Provide expert guidance to internal teams and sponsor clients on ICH and FDA regulatory frameworks, including CFR and GCP requirements.
• Collaborate cross-functionally with Clinical Operations, CMC, Pharmacovigilance, and Medical Writing to ensure cohesive and high-quality submission content.
• Maintain awareness of changes in regulatory requirements and provide proactive communication and strategic recommendations to internal and external stakeholders.
• Support business development by contributing to proposals, capabilities presentations, and bid defense meetings requiring regulatory input.

Work Location

This job will be 100% home-office based. (see Telecommuting Policy for full details)

Requirements

Preferred experience includes :

Why You Should Apply

QPS, LLC is an Equal Employment Opportunity / Affirmative Action Employer.