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. 0+ years of experience Preferred Qualifications 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. Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com Work Flexibility Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location. Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based. Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category. Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

Internal Clinical Research Associate.

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