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CRA II

System One

Remote · USContract / Full-time$40–50/hrSeen todaySeen in employer's feed today

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At a glance

Compensation
$40–50/hr
Location
Remote · US
Schedule
Contract / Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The CRA II will support clinical studies for a medical device organization, with ownership and visibility within Clinical Operations. The role covers study start-up, site readiness, monitoring, documentation, and coordination across concurrent studies. It is remote for candidates local to an airport and includes travel two to four times per month, depending on need.

Skills & qualifications

RequiredNice to have

Skills

Clinical MonitoringClass III Medical DevicesICU ExperienceSite ManagementTravel

Qualifications

Bachelor's Degree or RN2+ Years Monitoring Experience3+ Years Clinical Research Coordinator Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full job description

Job Title: CRA II

Location: Remote, local to an airport

Type: 3 month Contract

Compensation: $40-$50/hr

Work Model: Remote

Hours: 40 hours/week

Looking for your next step as a CRA? This is an opportunity to join a fast-moving medical device organization where you'll have meaningful ownership, strong visibility within Clinical Operations, and the ability to contribute to studies that can directly impact patient outcomes.

Responsibilities

  • Maintain TMF and regulatory documentation ensuring ICH/GCP and SOP compliance; oversee IRB approvals, informed consent quality, investigational device accountability, and complete/accurate reporting of AEs and protocol-required data.

  • Support study start-up and site readiness, conduct site training, manage study supplies and tracking systems, resolve queries/DCFs, and identify/implement corrective actions for protocol deviations across multiple concurrent studies.

  • Drive communication through team meetings, status reporting, and milestone tracking; support audits and site payments, lead documentation updates, and contribute to SOP enhancements and operational best practices.

Requirements

  • Bachelor’s Degree, or RN required

  • 2+ years monitoring experience

  • 3+ Clinical Research Coordinator experience

  • Class III Medical Device experience required

  • ICU (and therefore hospital) and site management experience required

  • Ability to travel 2-4 times/month (depends on volume of need)

System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M-

#LI-IF1

Ref: #568-Clinical

System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

How this job compares

Set against the 575 open Clinical Research Associate jobs on Olive Jobs, counted November 6, 2026.

Pay
  • This posting$40–50/hr
  • US median$56–62/hr39 hourly ranges

This range's midpoint, $45/hr, is 24% below the US median midpoint ($59/hr) — in the middle half of Clinical Research Associate hourly ranges across the US.

Openings
Olive Jobs lists 17 open Clinical Research Associate jobs in Illinois and 575 across the US. 24% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 3 years of experience — more than three in four Clinical Research Associate postings that state a minimum ask for (median 2 years, across 509 postings).
Education
146 of the 575 open Clinical Research Associate jobs (25%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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