Internal Clinical Research Associate
Key Skills for This Role
Full Job Posting
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
About Stryker
Stryker is a global medical technology company offering innovative products and services in surgical equipment, neurotechnology, orthopaedics, and spine care.
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