Position Summary:

We are seeking an experienced and strategic Associate Director, Analytical Development, to lead the execution of small molecule analytical activities across clinical and commercial programs. This role partners closely with the Director to shape and implement analytical strategies while driving day-to-day execution through external partners.

The Associate Director provides technical leadership across analytical activities, ensures alignment with regulatory expectations, and contributes to the progression of programs from early development through commercialization. This role collaborates cross-functionally with CMC, Quality, Regulatory, and external partners to ensure timely and high-quality deliverables.

This is a hybrid role (2-3 days in office) at our Waltham, MA headquarters.

Responsibilities:

• Lead execution of phase-appropriate analytical development strategies in alignment with Director guidance for external partners (CMOs/CROs), ensuring quality, timelines, and alignment with program goals
• Oversee analytical method development, qualification, validation, and transfer activities to support clinical and commercial programs
• Partner cross-functionally and external analytical partners to advance programs, escalating risks and proposing solutions proactively
• Provide technical review and guidance on analytical data, protocols, and reports to ensure scientific rigor and compliance
• Participate in the author and review of analytical sections of regulatory submissions (INDs, NDAs) in collaboration with senior leadership
• Represent the Analytical Development function on various cross-functional project teams including internal project teams as well as third-party analytical and manufacturing teams
• Ensure analytical activities are aligned with regulatory expectations and internal quality standards
• Contribute to continuous improvement initiatives, including processes, workflows, and vendor management practices

Qualifications:

• B.S. in chemistry or related discipline with 9+ years of industry or equivalent experience
• Demonstrated experience in analytical method development and validation as well as associated regulatory requirements
• Experience working in close collaboration with technical, regulatory, quality assurance, project management, and supply chain functions in a cGMP operational environment
• Experience in managing outsourced Analytical Development activities
• Experience in preparing regulatory documents including briefing books for regulatory meetings, INDs, and NDAs
• Excellent communication skills and the ability to present to internal and external audiences
• Strong understanding of cGMP requirements and quality systems related to analytical development activities
• Periodic travel to manufacturing and other partner sites (approximately 10% of time)

The anticipated annualized base pay range for this full-time position is $183,000 - $223,000 Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.

Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision), life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.