Regulatory Systems Manager

Ardelyx

Newark, CA

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JOB DETAILS

SALARY

$117,000–$143,000 Per Year

JOB TYPE

Full-time

SKILLS

Acceptance Testing, Biology, Biotech and Pharmaceutical, Change Control, Configuration Management, Corporate Policies, Cross-Functional, Data Management, Data Quality, Detail Oriented, Document Archiving, Document Management, Documentation, Employee Benefits, GxP, Health Plan, Identify Issues, Incentive Programs, Information Technology & Information Systems, Insurance, Operational Support, Prescription Drugs, Process Improvement, Product Lifecycle Management, Publishing Software, Regulations, Regulatory Compliance, Regulatory Requirements, Regulatory Submissions, Standard Operating Procedures (SOP), System Operations, System Test, System Validation, Systems Administration/Management, Team Player, Testing

LOCATION

Newark, CA

POSTED

1 day ago

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients. Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive. We foster an inclusive environment where employees are respected, supported, and empowered to make an impact — both within our company and in the lives of patients we serve.Position Summary: The Regulatory Systems Manager is responsible for the administration, optimization, and day-to-day management of regulatory systems that support global regulatory operations. This role will ensure regulatory information and documentation are maintained accurately and efficiently across systems that support regulatory submissions, health authority interactions, and product lifecycle management.This position is hands-on working closely with Regulatory Affairs, Quality, and IT teams. The Regulatory Systems Manager will play a key role in improving processes, ensuring data integrity, supporting system implementations, configuration, or upgrades, and enabling efficient regulatory submissions and compliance. Responsibilities: Serve as the primary business owner and administrator for regulatory systems (e.g. regulatory information management systems, document management systems, and submission publishing tools)Manage system configuration, user access, permissions, workflows, and data governance to ensure accurate and compliant regulatory recordsOversee system upgrades, releases, validation activities, and change control processes, including maintaining regulatory product data, submission data, and health authority correspondence within systemsDevelop and maintain standard operating procedures (SOPs), system documentation, and training materialsSupport the preparation and management of global regulatory submissions by ensuring systems and document structures align with submission requirementsPartner with Regulatory Affairs teams to track global regulatory commitments, submissions, approvals, and lifecycle activitiesEnsure global regulatory documentation is properly archived and maintained in accordance with company policies and regulatory requirementsProvide user training and ongoing support for regulatory teams using Veeva RIM (Registrations, Submissions, or Archive modules)Act as the point of contact for system questions, troubleshooting, and process guidance and vendor coordinationAct as the Regulatory Affairs representative in systems improvement projects with IT and external vendors, including performing system testing, validation support, and user acceptance testing (UAT)Ensure regulatory systems operate in compliance with applicable regulatory requirements and internal policiesQualifications: Bachelor’s degree in regulatory affairs, information systems, or related field with 5+ years of experience in regulatory operations or regulatory systems, or equivalent experience within the pharmaceutical, biotech, or life sciences industry.Experience administering and/or supporting regulatory systems such as Veeva Vault RIM, particularly Registrations and regulatory data management, or submission publishing toolsExperience supporting global regulatory submissions and product registration trackingStrong understanding of regulatory operations and regulatory document lifecycleExperience working in GxP regulated environmentsStrong attention to detail with focus on data integrity and complianceExcellent organizational, communication, and cross-functional collaboration skillsExperience supporting system implementations, configuration, or upgrades is preferredCertification or training in Veeva Vault platformThe anticipated annualized base pay range for this full-time position is $117,000 - $143,000. 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. Ardelyx is an equal opportunity employer.

About the Company

Ardelyx

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