Associate Director, Clinical Quality Assuranc

We are seeking a motivated and qualified individual to join our team as an Associate Director, Clinical Quality Assurance. This role provides strategic and operational leadership for the Clinical QA function, ensuring the highest standards of Good Clinical Practice (GCP) compliance across all clinical programs. This role is responsible for building and maintaining a robust, risk-based quality framework that supports all stages of clinical development, regulatory submissions, and sustained inspection readiness. The role will serve as a key partner across functions, driving a culture of quality, compliance, and continuous improvement.

Develop and execute the Clinical QA strategy aligned with organizational and development goals

Develop, implement, maintain and continuously improve phase-appropriate, risk-based clinical. quality systems, processes, SOPs and policies to support early and late phase clinical trials and regulatory submissions.

Implement proactive, risk-based approaches to identify, assess, and mitigate quality and compliance risks.

Provide ongoing GCP quality oversight and support to ensure adherence to global GCP, quality and compliance requirements across all clinical programs.

Partner closely with Clinical Operations, Clinical Development, Regulatory Affairs, Data Management, Biometrics, CMC, Clinical Supply Chain and study teams to proactively identify and mitigate compliance risks and ensure operational compliance.

Provide Clinical QA oversight for CROs, laboratories, and other clinical vendors. Ensure appropriate qualification, monitoring, and oversight are in place.

Review and contribute to key clinical and regulatory documents including INDs, protocols, IBs, NDAs, and other trial and submission-related materials, as applicable.

Lead the planning and execution of a comprehensive, risk-based GCP audit program (investigator sites, CROs, vendors, and processes).

Oversee the management of audit findings and drive effective CAPA implementation.

Oversee and support investigations of deviations, noncompliance and quality events, ensuring thorough root cause analysis, CAPA implementation and proper documentation.

Lead organizational inspection readiness activities for late phase programs and global regulatory authority inspections (e.g., FDA, EMA).

Ensure systems are inspection-ready and aligned with evolving regulatory expectations.

Serve as Clinical QA lead for regulatory inspections, including preparation, hosting, and post-inspection response management.

Support NDA/BLA/MAA submission activities from a quality perspective.

Influence and embed quality principles across the clinical development lifecycle.

Develop and deliver annual GCP training programs and quality-related trainings.

Communicate regulatory changes, best practices and compliance expectations to internal stakeholders.

Collaborate closely with the broader Quality team to execute Quality objectives and ensure alignment across GxP areas.

Foster a culture of inspection readiness and continuous improvement across the organization

Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis.

Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

Approximately 10-20% travel may be required.

Bachelor’s degree in life sciences, pharmacy, or related field; advanced degree preferred

10+ years of progressive GCP Quality Assurance experience in the biotechnology or pharmaceutical industry

Direct experience supporting late-stage clinical trials (Phase 2/3) and NDA/MAA submission preparation, with proven inspection readiness experience

Expert knowledge of global GCP regulations and guidance, including but not limited to:

21 CFR Parts 11, 50, 54, 56, 312

EU Clinical Trial Regulation (EU-CTR)

ICH E6(R2/R3), ICH E8

General Data Protection Regulation (GDPR)

Good Clinical Laboratory Practice (GCLP)

Extensive experience leading GCP audits (internal, investigator sites, CROs, and vendors) and managing regulatory inspections

Demonstrated ability to operate both strategically and hands-on in a small, fast-paced biotech environment

Excellent communication, collaboration, and influencing skills across cross-functional teams

Strategic mindset with strong execution capability

Deep expertise in GCP and clinical development processes

High integrity and commitment to quality and compliance

Strong leadership and stakeholder influence

Solutions-oriented with a proactive, risk-based approach

This is a full-time position, Monday-Friday, occasional overtime.

Pay is commensurate with experience.

Equity-based compensation

Performance-based bonuses

401(k) with Company Match

Medical, Dental, Vision

Flexible Spending Account

Life Insurance

Employee Assistance Program

Employee Discounts

Gym Membership

Paid Vacation

Paid Holidays

Paid Sick, Jury Duty, Bereavement

United States (Required)

Background Check

As a condition of employment, you must successfully complete all post-offer, pre-employment requirements, including but not limited to a background check.

ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system.

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law.

Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses.

Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.