Internal Clinical Research Associate
- Location
- Waltham, Massachusetts
- Work mode
- On-site
- Employment type
- Full-time
About the job
Work Flexibility: Onsite
Internal Clinical Research Associate Waltham, MA
Join a clinical research team that supports the execution of medical device clinical studies from study start-up through closeout. As an Internal Clinical Research Associate, you will contribute to clinical trial operations, study documentation, device accountability, data review, and regulatory compliance activities that help ensure studies are conducted according to established quality and regulatory standards.
What You Will Do
- Support site qualification, activation, monitoring, and closeout activities across multiple clinical studies.
- Manage investigational device accountability, including product serialization, inventory tracking, shipment coordination, and maintenance of device records.
- Maintain Trial Master Files and essential study documentation to support inspection readiness and regulatory compliance.
- Review, organize, and maintain informed consent forms, case report forms, and other study-related documents.
- Perform remote source data verification and study data review activities to support data quality and protocol compliance.
- Develop and maintain study metrics, reports, and dashboards that provide visibility into study progress and operational performance.
- Coordinate clinical trial registration activities and support audit and inspection preparedness efforts.
- Create study communications, newsletters, and documentation that support investigator sites and cross-functional study teams.
What You Will Need Required Qualifications
• Bachelor’s degree in Life Sciences, or a related scientific discipline.
- Bachelor’s degree in Life Sciences, or a related scientific discipline.
- 0+ years of experience
- Experience in clinical research, clinical trial operations, or clinical study administration.
- Experience working under Good Clinical Practice (GCP) guidelines.
- Experience using electronic clinical trial databases, clinical trial management systems, or related research software.
- Experience supporting clinical trial audits, regulatory inspections, or regulatory submission activities.
- Experience with clinical trial registration platforms and study reporting processes.
US20 : $87,000 - $145,100 USD Annual
Travel Percentage: 0%
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.
From Stryker's careers page (Workday), checked 29 Oct 2026.
How to apply
- Select Apply on stryker.com. It opens Stryker's own application form in a new tab, run on Workday.
- Fill in the form and upload your résumé there. Jobiwork never sees your application.
- Stryker will reply to you directly. No real employer asks you for money to apply.
Posted 22 Oct 2026 · checked 29 Oct 2026 · Report this job