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Circuit Clinical Jobs (NOW HIRING)

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Clinical Perfusionist

Azusa, CA

$121K - $174K/yr

The Clinical Perfusionist is a specialized medical professional responsible for preserving and ... circuit. 4. Maintain detailed and accurate documentation in donor medical records. 5. Coordinate ...

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Circuit Clinical information

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$14

$34

$90

How much do circuit clinical jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for circuit clinical in the United States is $34.62, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $32.93 per hour, depending on experience, location, and employer.

What is Circuit Clinical and what does the company do?

Circuit Clinical is a healthcare technology company focused on making clinical trials more accessible to patients and healthcare providers. They partner with medical practices and health systems to connect patients with research opportunities and streamline the trial process. By leveraging technology and a network of clinical research sites, Circuit Clinical aims to improve patient access, diversify trial participation, and make it easier for healthcare professionals to offer clinical research as a care option.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate, and why are they important?

To thrive as a Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical trial protocols, and often a relevant degree such as a BSN or BSc. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and regulatory compliance tools is typically required. Strong organizational skills, attention to detail, and effective communication set top candidates apart in this role. These competencies ensure the integrity, accuracy, and ethical conduct of clinical research, which are critical for advancing medical science and patient safety.

What is the difference between Circuit Clinical vs Clinical Research Coordinator?

AspectCircuit ClinicalClinical Research Coordinator
Required CredentialsBachelor's degree, clinical research experienceBachelor's degree, clinical research experience
Work EnvironmentHealthcare settings, clinical trial sitesHospitals, research institutions, clinical trial sites
Employer & Industry UsageHealthcare technology companies, clinical trial platformsHospitals, academic medical centers, research organizations
Common Search & ComparisonYesYes

Both Circuit Clinical and Clinical Research Coordinators require similar credentials and work in clinical trial environments. Circuit Clinical often operates within healthcare technology platforms, focusing on connecting patients with trials, while Clinical Research Coordinators typically work directly within hospitals or research institutions managing trials. Understanding these differences helps job seekers identify roles aligned with their experience and career goals.

What are some common challenges faced by professionals working at Circuit Clinical, and how can new hires best prepare for them?

Professionals at Circuit Clinical often work at the intersection of clinical research and technology, which can pose challenges such as adapting to rapidly evolving digital tools and balancing regulatory compliance with innovation. New hires should be prepared to collaborate closely with cross-functional teams, including clinicians, data scientists, and regulatory experts. Staying proactive about learning new platforms and maintaining open communication within the team can help ease the transition. Embracing a continuous learning mindset and seeking mentorship within the company are excellent ways to overcome these challenges and thrive in the role.
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Circuit Clinical jobs near you
Contract Principal Investigator

Contract Principal Investigator

Circuit Clinical

Middletown, NY

$120 - $150/hr

Other

Posted 15 days ago

Job description

Description

Circuit Clinical is on a mission to transform the way people find, choose, and participate in clinical research. 


We are searching for a Contract Principal Investigator. 


This position is ultimately responsible for research project feasibility, research project start-up, screening visits, research project maintenance and follow up, research project closeout, and post-closeout safety follow-up. 


You'll Be Responsible For: 

  • Serve as PI for industry sponsored clinical research trials 
  • Maintain ultimate regulatory responsibility for study conduct, subject safety, and protocol compliance 
  • Appropriately delegate study related activities to qualified research staff while providing ongoing oversite according to FDA regulations, local regulations, and ICH/GCP guidelines 
  • Provide medical oversight 
  • Review Adverse Events and Serious Adverse Events 
  • Confirm patient eligibility as defined in the research protocol 
  • Complete study assessments as required (i.e. physical exam) 
  • Participate in the consenting process and patient's clinical research education 
  • Attend monitoring visits (Pre-study, Initiation, Interim and Close Out) on assigned studies 
  • Complete GCP/HSP, study specific, and system specific training per protocol and Circuit Clinical IT guidelines 
  • Participate in relevant study team meetings both internal and with the sponsor/CRO 
  • Participate in webinars and PI meetings as needed 

Your Qualifications: 

  • MD or DO License is required 
  • A Medical License in good standing in NY 
  • At least 1 year of experience working in clinical research. 
  • Experience in vaccine clinical trials preferred. 

The fine print: 

Location: This position is an on-site position working in our Middletown, New York site.

Employment: This is an independent contractor position working 15-20 hours per week, which could develop to 40 hours per week.

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