Internal Clinical Research Associate - Remote at Stryker
Why join Stryker?
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards – not to mention various social and recreational activities, all of which are location specific.
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.
Internal Clinical Research Associate – Remote
As an Internal Clinical Research Associate, you will support key clinical trial activities from site activation through study closeout, helping ensure studies are conducted in accordance with regulatory requirements, quality standards, and clinical research best practices.
What You Will Do
- Support site identification, qualification, activation, monitoring, and closeout activities across clinical studies.
- Maintain Trial Master Files and essential study documents to ensure inspection readiness and regulatory compliance.
- Partner with clinical study teams to develop, review, and manage study documentation required for trial execution.
- Review and maintain informed consent forms, case report forms, and other study-related materials.
- Generate study newsletters and communications to support investigator sites and cross-functional stakeholders.
- Track and support study invoicing activities and maintain associated documentation.
- Create and maintain study metrics, reports, and dashboards to support clinical trial oversight and execution.
- Support clinical trial registration, audit preparation, data collection activities, and adherence to regulatory and Good Clinical Practice requirements.
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 platforms.
- Experience supporting clinical trial audits, inspections, or regulatory submissions.
- Experience with clinical trial registration platforms and study reporting activities.
Posted Date: 07/09/2026
This role will be posted for a minimum of 3 days.
United States of America Pay Ranges
- USN: $72,500 - $120,900 USD Annual
- US5: $76,100 - $126,900 USD Annual
- US10: $79,800 - $133,000 USD Annual
- US15: $83,400 - $139,000 USD Annual
- US20: $87,000 - $145,100 USD Annual
- US30: $94,300 - $157,200 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.
Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insurance, hospital indemnity insurance, personalized healthcare support, wellbeing program and tobacco cessation program. Financial benefits include: Health Savings Account (HSA), Flexible Spending Accounts (FSAs), 401(k) plan, Employee Stock Purchase Plan (ESPP), basic life and AD&D insurance, and short-term disability insurance. Stryker offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually. Depending on customer requirements employees and new hires in sales and field roles that require access to customer accounts as a function of the job may be required to obtain various vaccinations as an essential function of their role.
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