Internal Clinical Research Associate
Stryker
About the Role
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.
Key Responsibilities
- 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.
Requirements & Tech Stack
- Bachelor’s degree in Life Sciences, or a related scientific discipline.
- 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.