Senior Clinical Research Associate
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Stryker
Baton Rouge, LA (In Person)
$111,050 Salary, Full-Time
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Job Description
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
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
- not to mention various social and recreational activities, all of which are location specific.
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 Posting Date:
05/19/2026Posted Date:
05/19/2026 This role will be posted for a minimum of 3 days.United States of America Pay Ranges:
USN :
$83,300- $138,800 USD Annual US5 : $87,500
- $145,700 USD Annual US10 : $91,600
- $152,700 USD Annual US15 : $95,800
- $159,600 USD Annual US20 : $100,000
- $166,600 USD Annual US30 : $108,300
- $180,400 USD Annual View the U.
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.Similar jobs in Baton Rouge, LA
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