Revolution Medicines

Associate Director, Regulatory Systems

Revolution Medicines$186K — $233K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Information Systems, or related field.
  • 8+ years of experience in Regulatory Systems or related domains.
  • Hands-on experience with RIM platforms (e.g., Veeva RIM) and DocuBridge.
  • Strong understanding of regulatory submission processes and document management workflows.
  • Experience with GxP validation frameworks (GAMP5, 21 CFR Part 11, Annex 11).
  • Strong analytical, problem-solving, and communication skills.

Responsibilities

  • Act as system owner for Veeva RIM and DocuBridge, ensuring compliance with Regulatory Affairs.
  • Lead implementation and optimization of regulatory systems.
  • Collaborate with stakeholders to translate business needs into system functionalities.
  • Maintain system governance including change control and documentation management.
  • Ensure systems meet GxP validation and compliance requirements.
  • Develop training materials and promote best practices for end-users.
  • Support audits related to RIM and document management systems.

Benefits

  • Comprehensive equity awards.
  • Robust learning and development opportunities.
  • Flexible hybrid working arrangements.
Full Job Description
The Opportunity:

The Associate Dir, RIM & DocuBridge Systems will serve as the system owner for Veeva RIM and DocuBridge platforms, supporting global regulatory operations. This role will be responsible for driving system strategy, ensuring compliance, and optimizing processes to enable efficient and scalable regulatory submissions and document management.

Key Responsibilities:
  • Serve as system owner for Veeva RIM and DocuBridge platforms, ensuring alignment with Regulatory Affairs processes.
  • Lead system implementations, enhancements, and ongoing optimization efforts.
  • Partner with Regulatory Affairs and cross-functional stakeholders to gather and translate business requirements into system solutions.
  • Ensure systems are validated and maintained in compliance with GxP requirements (e.g., 21 CFR Part 11, Annex 11, GAMP5).
  • Establish and maintain system governance, including change control, release management, and documentation.
  • Support integration with related systems (e.g., eTMF, Quality, Safety, Clinical systems).
  • Collaborate with vendors to support system performance and issue resolution.
  • Develop training materials and support end-user adoption and best practices.
  • Support audits and inspections related to RIM and document management systems.

Required Skills, Experience and Education:
  • Bachelor's degree in Life Sciences, Information Systems, or related field.
  • 8+ years of experience in Regulatory Systems or related domains.
  • Hands-on experience with RIM platforms (e.g., Veeva RIM) and document management systems such as DocuBridge.
  • Strong understanding of regulatory submission processes and document management workflows.
  • Experience with GxP validation and compliance frameworks (GAMP5, 21 CFR Part 11, Annex 11).
  • Demonstrated ability to manage cross-functional stakeholders and system implementations.
  • Strong analytical, problem-solving, and communication skills.

Preferred Skills:
  • Experience with global regulatory submissions (eCTD) and health authority requirements.
  • Familiarity with integrations across RIM, eTMF, and other clinical/regulatory systems.
  • Experience with vendor management and managed services models.
  • Experience supporting system strategy and roadmap planning.
    #LI-Hybrid #LI-YG1


The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

Base Pay Salary Range

$186,000-$233,000 USD

We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.

Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official @revmed.com email address.

If you believe you've been contacted by someone impersonating a Revolution Medicines recruiter, please report it to [email protected] so we can share these impersonations with our IT team for tracking and awareness.

About Revolution Medicines

Revolution Medicines is a clinical-stage precision oncology company focused on developing targeted therapies to inhibit elusive frontier targets within notorious growth and survival pathways, with particular emphasis on RAS and mTOR signaling pathways. The company's proprietary platform enables the discovery and development of small molecules that bind covalently to proteins. Revolution Medicines was founded in 2014 and is headquartered in South San Francisco, California.
Learn more about Revolution Medicines
Size
201 employees
Market Cap
$2.1 billion
Industry
Net Income
-$108.1 million
Revenue
$42.9 million
NASDAQ

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