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Senior Manager, Clinical Systems and Processes

Job in Phoenix, Maricopa County, Arizona, 85003, USA
Listing for: Crinetics Pharmaceuticals
Full Time position
Listed on 2026-07-08
Job specializations:
  • IT/Tech
    Change Management, IT Project Manager
Salary/Wage Range or Industry Benchmark: 137000 - 171000 USD Yearly USD 137000.00 171000.00 YEAR
Job Description & How to Apply Below
Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline.

We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world’s premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others.

Position Summary:

The Senior Manager, Clinical Systems and Processes will serve as a key subject matter expert (SME) responsible for driving the design, implementation, and continuous improvement of clinical systems and processes across Clinical Operations. This role will provide advanced oversight and expertise across Veeva Vault Clinical Suite (TMF, CTMS, Site Connect, Study Start-up), Veeva Study Training, Smartsheet, Risk-Based Quality Management (RBQM) frameworks, and emerging Artificial Intelligence (AI) solutions.

The incumbent is also responsible for change management, solutions adoption, and clinical system lifecycle management. The Senior Manager provides clinical oversight for computer systems validation (CSV), Computer Software Assurance (CSA), system change control, vendor governance, and clinical technology product roadmap activities in compliance with GxP and 21 CFR Part 11 requirements. This individual will partner closely with the Director, Clinical Systems and Processes to develop and scale departmental capabilities.

The incumbent will ensure that all clinical systems and processes are managed in accordance with ICH/GCP guidelines, relevant regulations, and Crinetics SOPs, while fostering a culture of innovation, quality, and operational excellence.

Essential Job Functions and Responsibilities:

These may include but are not limited to:

Execute strategy and lead implementation or system enhancement of clinical systems including Veeva Vault Clinical Suite (TMF, CTMS, Site Connect, Study Start-up), Veeva Study Training, Smartsheet, and other Clinical Operations platforms such as RBQM.Oversee and mentor the Manager, Clinical Systems and Processes, providing guidance, and supporting daily clinical systems and processes activities in alignment with leadership expectations.

Serve as a primary SME on behalf of Clinical Operations for Veeva Vault Clinical Suite system configurations, architecture, and backend administration, including expert-level knowledge of the Veeva Vault Clinical Suite.

Support the evaluation, piloting, and adoption of Artificial Intelligence (AI) solutions to enhance Clinical Operations efficiency, data quality, and decision-making capabilities.

Support the development of an RBQM platform to enable the development of dashboards, visualizations, and tools for proactive risk identification and centralized monitoring execution across clinical studies.

Lead systems integration initiatives across clinical platforms, ensuring seamless data flow, interoperability, and alignment with enterprise-wide technology strategies.

Develop and execute organizational change management plans to support the successful rollout and adoption of new systems, processes, and technology solutions across internal and external stakeholder groups. This includes stakeholder engagement, user training programs, communication strategies, and post-implementation support.

Oversee system-level change control and validation activities for clinical systems in compliance with GxP, 21 CFR Part 11, and SDLC standards, including impact assessments, user acceptance testing (UAT), configuration records, and associated documentation.

Support maintenance of the clinical systems product roadmap by contributing to release planning, system upgrade cycles, system…
Position Requirements
10+ Years work experience
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