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Open nowPosted today

Clinical Research Associate II

Stryker1,440 open roles

Where
Mahwah, New Jersey
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Your applicationOpen nowClinical Research Associate IIStryker · Mahwah, New Jersey

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The clock on this job

Early applications get read.

14.0% of postings close within 7 days. Measured by our own scanner across the market. Stryker postings stay open a median of 20 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.7%3 days
  3. 14.0%7 days
  4. 22.5%14 days
  5. 38.3%30 days
  6. 59.0%60 days
This job: posted today

Stryker median: 20 days open

The posting

Work Flexibility: Hybrid

Stryker is hiring a Clinical Research Associate II for our Joint Replacement division. This is a hybrid role based in Mahwah, NJ requiring up to 40% travel.

As the Clinical Research Associate II, you will support clinical studies through hands-on site monitoring and study management. In this role, you will serve as a primary contact for clinical research sites and oversee activities across the study lifecycle, helping ensure clinical data integrity and compliance with applicable regulatory requirements, study protocols, and company procedures.

What You Will Do

  • Manage assigned clinical research sites throughout the study lifecycle, serving as the primary point of contact for site personnel.
  • Conduct site qualification/selection assessments, site initiation, interim monitoring, and closeout visits independently and document findings within required timelines.
  • Monitor clinical study data and source documentation to verify accuracy, completeness, traceability, and compliance with study protocols.
  • Evaluate site activities against Good Clinical Practice, FDA, ISO, and other applicable clinical research and regulatory requirements.
  • Identify, document, and follow up on protocol deviations, data discrepancies, compliance issues, and corrective actions through resolution.
  • Coordinate with investigators, clinical research coordinators, study teams, and cross-functional partners to support study execution and address site-level issues.
  • Maintain required clinical trial documentation and site records in accordance with study procedures, regulatory requirements, and established quality standards.
  • Track site progress, enrollment activities, monitoring findings, and outstanding deliverables to support study timelines and clinical trial objectives.

What You Need

Required

  • Bachelor’s degree in a science, healthcare, life sciences, or related field, or equivalent education.
  • Minimum 4 years of relevant clinical research experience, including direct clinical site monitoring experience.
  • Experience independently conducting site qualification/selection assessments, site initiation, interim monitoring, and/or closeout visits.
  • Experience applying Good Clinical Practice, FDA, ISO, or related clinical research requirements to clinical trial activities and documentation.

Preferred

  • Certified Clinical Research Associate (CCRA) certification.
  • Experience in the medical device or pharmaceutical industry.
  • Previous experience as a Clinical Research Associate, Clinical Research Coordinator, or Clinical Trial Coordinator.
  • Experience supporting orthopedic clinical research or orthopedic medical devices.
  • US20: $114,800 - $191,400 USD Annual

Travel Percentage: 40%

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.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

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