Senior Clinical Research Associate

Posted 2 Days Ago
Be an Early Applicant
Baton Rouge, LA, USA
In-Office
83K-180K Annually
Junior
Healthtech
The Role
The Senior Clinical Research Associate will manage site monitoring, ensure compliance with clinical protocols, and support clinical trials while traveling for site visits.
Summary Generated by Built In
Work Flexibility: Remote

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: 05/19/2026

  


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.S. work location and transparency guide to find the pay range for your location.

  


Travel Percentage: 50%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Skills 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 and management activities
  • Fundamental knowledge of GCPs, clinical study process, and logistics
  • Ability to apply ISO, FDA and related guidelines towards documentation
  • Experience as a Clinical Research Coordinator or Clinical Trial Coordinator
  • CCRA Certification

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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