Clinical Research Associate II

Imperative Care

📍Campbell, CA
Posted May 20, 2026

Job Overview

Position

Clinical Research Associate II

Company

Imperative Care

Location

Campbell, CA

Work Type

On-site

Job ID

li-4417010898

Job Description

Title: Clinical Research Associate II
*Location*
*:*
*This position is based in our Campbell, California offices. This position is on-site, full-time + Travel Considerations.*
Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke and vascular diseases are treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.

What You’ll Do
Provide in-house clinical operations support by assisting with study documentation, site coordination, and day-to-day clinical trial activities to help ensure successful study execution.

  • Support the preparation, organization, and maintenance of essential clinical study documentation and study files

  • Coordinate with clinical sites and internal teams to support ongoing study activities and communication

  • Conduct clinical monitoring and data verification activities to ensure high-quality study execution and data integrity across trial site

  • Review study documentation for completeness, accuracy, and compliance with company and regulatory standards

  • Provide operational and administrative support to the clinical team in a fast-paced medical device environment

What You’ll Bring

  • Bachelor’s degree in life sciences or related field with 1–3 years of clinical research or medical device experience

  • Basic understanding of FDA regulations, ICH-GCP guidelines, and clinical trial processes

  • Strong organizational skills with high attention to detail and documentation accuracy

  • Excellent communication and collaboration skills with the ability to manage multiple priorities

  • Self-motivated, adaptable, and eager to grow within a clinical research and operations environment

Employee Benefits
include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.

Salary Range: $101,000 - 106,000 annually

Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.

Join Us!
Apply Today
The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.

Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.

Interview Prep

AI-powered insights to help you prepare

Key Skills

Required:
Preferred:

Practice Questions

💡Technical Questions (3)
  • 1.How do you ensure data integrity and compliance with ICH-GCP guidelines when conducting clinical monitoring and data verification at a trial site?
  • 2.Can you walk me through your process for preparing, organizing, and maintaining essential clinical study documents, such as the Trial Master File (TMF)?
  • 3.Given that this role is in the medical device sector, how does the regulatory landscape for device trials differ from pharmaceutical trials, particularly regarding FDA regulations?
🎯Behavioral Questions (3)
  • 1.Tell me about a time you had to manage multiple high-priority tasks or studies simultaneously in a fast-paced clinical environment. How did you ensure nothing fell through the cracks?
  • 2.Describe a situation where you identified a compliance issue or documentation error during a review. How did you handle it?
  • 3.Give an example of how you effectively coordinated communication between a clinical site and an internal team to resolve an operational challenge.
🧩Situational Questions (2)
  • 1.You arrive at a clinical site for a monitoring visit and discover that the principal investigator has been signing off on documents without properly reviewing the source data. What do you do?
  • 2.You are supporting a fast-paced medical device study, and the internal team urgently requests a regulatory document for an upcoming audit, but you are also behind on site coordination emails. How do you prioritize and handle this?

Resume Keywords

Make sure these keywords appear on your resume

Clinical monitoringData verificationICH-GCPFDA regulationsSite coordinationMedical deviceTrial Master FileSource data verificationClinical operationsRegulatory complianceEssential documentsCross-functional collaboration

Interested in this position? Apply directly on LinkedIn.

Apply on LinkedIn →