Regulatory Systems Manager

United States·Newarkmid

Legal & ComplianceRegulatory

0 views0 saves0 applied

Apply Now

Quick Summary

Overview

Key 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,…

Requirements Summary

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.

Technical Tools

Legal & ComplianceRegulatory

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 records
Oversee system upgrades, releases, validation activities, and change control processes, including maintaining regulatory product data, submission data, and health authority correspondence within systems
Develop and maintain standard operating procedures (SOPs), system documentation, and training materials
Support the preparation and management of global regulatory submissions by ensuring systems and document structures align with submission requirements
Partner with Regulatory Affairs teams to track global regulatory commitments, submissions, approvals, and lifecycle activities
Ensure global regulatory documentation is properly archived and maintained in accordance with company policies and regulatory requirements
Provide 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 coordination
Act 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 policies

Qualifications:

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 tools
Experience supporting global regulatory submissions and product registration tracking
Strong understanding of regulatory operations and regulatory document lifecycle
Experience working in GxP regulated environments
Strong attention to detail with focus on data integrity and compliance
Excellent organizational, communication, and cross-functional collaboration skills
Experience supporting system implementations, configuration, or upgrades is preferred
Certification or training in Veeva Vault platform

The 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.