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Senior Clinical Research Associate

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Job description

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.

Stryker is seeking a Senior Clinical Research Associate (CRA I) to join our innovative Neurovascular division. This is a remote, U.S.‑based role offering meaningful growth opportunities for CRAs looking to deepen their clinical monitoring experience while supporting impactful clinical trials. The role includes approximately 50% travel, providing hands‑on exposure and strong site partnership.

As Senior Clinical Research Associate, you will support clinical studies end‑to‑end, gaining experience in site monitoring, documentation, and compliance while working closely with cross‑functional study teams.

What you will do

Perform site monitoring and site management responsibilities through all phases of clinical study (e.g. site selection, site initiation, interim monitoring, and closeout)
Conduct site visits for all phases (site qualification, site initiation, interim monitoring, and closeout)
Ensure site compliance to clinical study protocol, applicable regulations and guidelines
Ensure data integrity by verifying data in case report forms against source documents
Identify and support site in addressing any noncompliance issues.
Collect and track regulatory documents, maintain trial master file (TMF) documentation and ensure accuracy
Communicate relevant updates to study core team

What you need

Required

Bachelor's level degree or equivalent in science or health care field
2+ years of relevant clinical research experience
Demonstrated independence in performing site monitoring (e.g. site selection, site initiation, interim monitoring and closeout visits) and site management activities
Fundamental knowledge and good understanding of GCPs, clinical study development process, and logistics
Ability to apply ISO, FDA and related guidelines toward documentation

Preferred

Experience as a Clinical Research Coordinator, Clinical Trial Coordinator or Clinical Research Associate
CCRA Certification

$83,300.00 - $180,400.00 salary plus bonus eligible + benefits. Individual pay is based on skills, experience, and other relevant factors.

Posting Date: 04/09/2026

Posted Date: 04/09/2026
This role will be posted for a minimum of 3 days.

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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