Internal Clinical Research Associate - Remote

Posted Yesterday
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Hiring Remotely in Los Angeles, CA, USA
In-Office or Remote
73K-157K Annually
Entry level
Healthtech
The Role
Support clinical trial activities from site identification through closeout, maintain trial master files and regulatory documents, review consent/CRFs, produce communications and reports, assist invoicing, registration, audit prep, and ensure GCP compliance for study execution.
Summary Generated by Built In
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.

Skills Required

  • Bachelor's degree in Life Sciences or 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
  • Experience using electronic clinical trial databases or clinical trial management systems (EDC/CTMS)
  • Experience supporting clinical trial audits, inspections, or regulatory submissions
  • Experience with clinical trial registration platforms and study reporting activities

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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