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Internal Clinical Research Associate - Remote

Role overview

Qualifications

  • Bachelor’s degree in Life Sciences or a related scientific discipline
  • 0+ years of experience
  • Experience in clinical research, clinical trial operations, or clinical study administration
  • Experience working under Good Clinical Practice (GCP) guidelines

Responsibilities

  • 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
  • Generate study newsletters and communications to support investigator sites and cross-functional stakeholders

About the company

Stryker logo

Stryker

Stryker is a global leader in medical technologies and, together with our customers, we are driven to make healthcare better. We offer 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. More information is available at stryker.com and careers.stryker.com. Facts: ● 2023 Sales: $20.5 billion ● Industry: Medical Instruments & Supplies ● Employees: 52,000 worldwide ● 40 years of sales growth leading up to 2020 ● 44+ Manufacturing and R&D Locations Worldwide ● $1.4 billion spent on research and development in 2023 ● ~12,900 patents owned globally in 2023 ● Products sold in ~75 countries ● Fortune 500 Company ● 7 consecutive years as one of Fortune's World's Best Workplaces Stryker’s social media community guidelines: https://www.stryker.com/content/m/legal/social-media-community-guidelines/en/index.html Notice Regarding Employee Conduct on Facebook/LinkedIn Meta/LinkedIn does not permit employers to verify or validate “employees” in the (META: “Works at” LinkedIn: “Experience”) section of users’ profiles. Please be aware that the views expressed by individuals on their personal accounts and do not necessarily represent the views of our company. If you encounter any issues with a person claiming to be our employee, we recommend using the “Report Profile” feature. If you’d like to report concerns to our Ethics Hotline, you may do so at: https://app.convercent.com/en-us/LandingPage/b6bb4e84-9fcb-ea11-a974-000d3ab9f296

Company details

Company typeXLarge
Company size10001

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Job description

Work Flexibility: Remote

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.

  

 

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.

  

 

Travel Percentage: None

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.

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Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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