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Remote Cra Jobs in Remote, OR (NOW HIRING)

IT ENGAGEMENTS INC

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CRA/CPM Study Start-Up and Monitoring Support (Contract Role)

OR · Remote

$68 - $70/hr

CRA/CPM Study Start-Up and Monitoring Support (Contract Role) Location ... Remote Client is a global medical device leader pioneering incisionless focused ultrasound ...

IT ENGAGEMENTS INC

Be Seen First

CRA/CPM Study Start-Up and Monitoring Support (Contract Role)

OR · Remote

$68 - $70/hr

CRA/CPM Study Start-Up and Monitoring Support (Contract Role) Location ... Remote Client is a global medical device leader pioneering incisionless focused ultrasound ...

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Remote Cra information

See Remote, OR salary details

$11K

$79.4K

$137.4K

How much do remote cra jobs pay per year?

As of Sep 6, 2026, the average yearly pay for remote cra in Remote, OR is $79,358.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,400.00 per year, depending on experience, location, and employer.

What is a remote CRA?

Remote Clinical Research Associates (CRAs) are professionals who monitor clinical trials and ensure compliance with regulatory requirements, study protocols, and data integrity, all while working from a remote location. Unlike traditional CRAs who travel to clinical sites, remote CRAs use technology to oversee site activities, review data, and communicate with site staff virtually. This role is essential in supporting the effective and efficient execution of clinical trials, especially as remote monitoring becomes more common in the industry.

What does a remote CRA do?

The responsibilities of a remote clinical research associate (CRA) involve working to monitor research efforts and progress. During a project, the remote CRA ensures that the research team follows all necessary protocols and procedures. In this career, your responsibilities also include maintaining records of relevant data and findings and monitoring the process of the project. Since this is a remote position, you perform your duties from home or another location away from the research site. When working on a clinical drug trial or medical study, you review procedures and ensure that researchers document all necessary information to meet regulatory requirements.

What are the key skills and qualifications needed to thrive as a remote CRA, and why are they important?

To thrive as a Remote Clinical Research Associate, you need a solid background in life sciences or a related field, experience with clinical trials, and often a bachelor's degree or higher. Familiarity with electronic data capture (EDC) systems, regulatory compliance tools, and certifications such as ACRP or SOCRA are typically required. Exceptional organizational skills, attention to detail, and clear communication are essential soft skills for effective remote monitoring and collaboration. These skills are crucial to ensure protocol adherence, data integrity, and successful coordination of clinical studies from a remote setting.

What are some common challenges faced by remote CRAs, and how can they be managed effectively?

Remote Clinical Research Associates (CRAs) often face challenges such as maintaining clear communication with on-site teams, managing multiple study sites virtually, and ensuring data integrity without in-person monitoring. To address these, successful CRAs leverage robust digital tools for documentation and communication, schedule regular virtual check-ins with site staff, and stay organized with meticulous tracking systems. Proactive problem-solving and adaptability are key to ensuring trial protocols are followed and regulatory requirements are met while working remotely.

What is the difference between Remote Cra vs Remote Clinical Research Associate?

AspectRemote CraRemote Clinical Research Associate
CredentialsBachelor's degree in life sciences, clinical research experienceBachelor's degree, clinical trial knowledge, certification often preferred
Work EnvironmentHome-based, flexible schedules, virtual communicationPrimarily home-based, site visits may be required, virtual meetings common
Industry UsagePharmaceutical, biotech, CROsPharmaceutical companies, CROs, research organizations
Search & Comparison IntentYesYes

The Remote Cra and Remote Clinical Research Associate roles are similar in credentials, work environment, and industry usage. Both positions involve overseeing clinical trials remotely, requiring relevant education and experience. The main difference lies in terminology; 'Remote Cra' is often used interchangeably with 'Remote Clinical Research Associate,' but the latter may emphasize more formal certification and specific industry standards. Both roles are vital in advancing clinical research while offering flexible, remote work options.

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Remote Cra jobs near you
Infographic showing various Remote Cra job openings in Remote, OR as of July 2026, with employment types broken down into 91% Full Time, 6% Part Time, 1% Temporary, and 2% Contract. Highlights an 74% Physical, 4% Hybrid, and 22% Remote job distribution, with an average salary of $79,358 per year, or $38.2 per hour.

CRA/CPM Study Start-Up and Monitoring Support (Contract Role)

IT ENGAGEMENTS INC

OR • Remote

$68 - $70/hr

Contractor

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Greetings from IT Engagements

IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.


Role: CRA/CPM Study Start-Up and Monitoring Support (Contract Role)

Location: Remote

 

Client is a global medical device leader pioneering incisionless focused ultrasound therapies that treat neurological and other disorders without surgery. Our clinical team supports first-in-human, pivotal, and post-market studies across global sites.

 

Position Summary

Client is seeking a Clinical Research Associate who brings hands-on monitoring skills along with study start-up support experience, including contracts, budgets, and IRB/EC submissions. The CRA will work under the direction of the Clinical Project Manager, helping manage the administrative and regulatory workload of study start-up while also executing monitoring visits.

 

Key Responsibilities

Study Start-Up Support

  • Assist with site feasibility assessments and qualification visits (SQV/PSV) for new studies.
  • Help prepare and route Clinical Trial Agreements (CTAs) and other site contracts for CPM and Legal review.
  • Support site budget tracking and invoice reconciliation.
  • Prepare IRB/EC submission packages and track approvals and amendments.
  • Support ICF development and site-specific customization.
  • Track start-up timelines and flag delays to the CPM.

 

Clinical Monitoring

  • Conduct SIV, IMV, and COV visits per protocol, ICH-GCP, and ISO 14155 for device trials.
  • Perform SDV and SDR under both 100% SDV and risk-based monitoring (RBM) frameworks.
  • Monitor device-specific compliance: accountability, maintenance logs, and complaint/malfunction reporting.
  • Identify protocol deviations and help sites plan corrective actions.
  • Support timely query resolution.
  • Maintain trip reports, visit logs, and CTMS documentation in real time.

 

CPM Support

  • Help maintain study timelines, risk registers, and enrollment forecasts.
  • Support budget tracking against contracted milestones.
  • Support inspection readiness and audit response at the site level.

 

Required Qualifications

  • Bachelor's degree in life sciences, nursing, or related field (or equivalent experience).
  • 3+ years of clinical research experience spanning both study start-up support and monitoring.
  • GCP certification.
  • Exposure to CTAs, site budgets, and IRB/EC submissions, even in a supporting capacity.
  • Hands-on experience conducting PSV, SIV, IMV, and COV visits.
  • Experience with both 100% SDV and RBM models.
  • Proficiency with CTMS and EDC systems.
  • Comfortable supporting multiple sites/studies concurrently.
  • Able and willing to travel up to 70%.

 

Preferred Qualifications

  • Prior experience monitoring medical device or combination product trials.
  • Familiarity with focused ultrasound, neurology, or other device-driven therapeutic areas.

 


 

Thank You

vinaya [at] itengagements [dot] com