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Clinical Research Data Associate Manager

Stryker

Irvine, CAJob$110–183K/yrPosted 2 days agoSeen in employer's feed today

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At a glance

Compensation
$110–183K/yr
Location
Irvine, CA
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree

Job overview

Stryker is hiring a Clinical Research Data Associate Manager in its Peripheral Vascular business to lead clinical data management for complex, high‑visibility studies, providing strategic oversight, ensuring data quality, regulatory compliance, and mentoring junior team members.

Skills & qualifications

RequiredNice to have

Skills

Clinical Data ManagementSQLCRF/eCRF DesignDatabase PlanningData ReviewQuery ManagementDatabase FreezeStudy ReportingUATChange Control

Qualifications

Bachelor’s Degree6+ Years Clinical Data Management ExperienceLeadership Experience in Data ManagementExperience Leading End-to-End Clinical Data ManagementAdvanced CRF/eCRF Design Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Stryker is hiring an Clinical Research Data Associate Manager in our Peripheral Vascular business to serve as the clinical data management lead for complex, high-visibility clinical studies and programs. This role provides strategic oversight of data management activities across the study lifecycle, ensuring the delivery of high-quality, reliable, and regulatory-compliant clinical data. The Associate Data Manager is recognized as a subject matter expert in clinical data management and partners with cross-functional stakeholders to develop data collection strategies, drive operational excellence, manage vendors, and mitigate study risks. The position independently leads data management activities for multiple studies while contributing to departmental initiatives, process improvements, standards development, and mentoring junior team members.

What you will do

  • Lead clinical data management activities across the study lifecycle, including database planning, data review, query management, database freeze/lock readiness, study reporting, and study closeout activities.

  • Design, build, and maintain clinical databases, CRFs/eCRFs, workflows, edit checks, and data collection processes aligned with protocol requirements and study objectives.

  • Develop and execute data management plans, review strategies, timelines, and documentation to ensure data integrity, quality, compliance, and inspection readiness.

  • Establish and monitor key study milestones, including database go-live, interim analyses, database freezes, database lock, data transfers, and archival activities.

  • Lead data cleaning, review, and issue resolution activities by identifying trends, managing queries, investigating discrepancies, and implementing corrective actions to ensure accurate and reliable study data.

  • Collaborate with cross-functional stakeholders, including Clinical Operations, Clinical Insights, Safety, Biostatistics, Programming, and Regulatory Affairs, to support study execution, reporting, regulatory submissions, and data-driven decision making.

  • Support database validation, user acceptance testing (UAT), change control activities, and continuous improvement initiatives to enhance data management processes, standards, and system performance.

  • Generate data reports, metrics, dashboards, and study summaries; provide training, guidance, and oversight to study personnel and data management team members to promote consistent data quality practices.

What you need

Required Qualifications

  • Bachelor’s degree

  • Minimum of 6+ years of clinical data management experience supporting clinical trials in the medical device, medical technology, or pharmaceutical industry.

  • Experience leading or contributing to departmental initiatives, strategic planning efforts, or organizational improvement projects.

  • Demonstrated experience independently leading data management activities across multiple complex clinical studies.

Preferred Qualifications

  • Experience leading end-to-end clinical data management activities across multiple studies and throughout the study lifecycle.

  • Advanced experience with CRF/eCRF design, clinical database development, edit check specification, validation, and UAT.

  • Proficiency with SQL and/or other data review and reporting tools used to identify trends, data quality issues, and opportunities for process improvement.

Posted Date: 10/01/2026

This role will be posted for a minimum of 3 days.

United States of America Pay Ranges:

  • USN : $110,100 - $183,400 USD Annual

  • US5 : $115,600 - $192,600 USD Annual

  • US10 : $121,100 - $201,700 USD Annual

  • US15 : $126,600 - $210,900 USD Annual

  • US20 : $132,100 - $220,100 USD Annual

  • US30 : $143,100 - $238,400 USD Annual

View the U.S. work location and transparency guide (https://view.stryker.com/viewer/fcd609f31e39eac44598615224ec7216?iid=69deda99678eb495e0710914#1) to find the pay range for your location.

Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

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