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Remote Clinical Data Reviewer Jobs in Remote, OR

IT ENGAGEMENTS INC

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

OR · Remote

$68 - $70/hr

Remote Client is a global medical device leader pioneering incisionless focused ultrasound ... and route Clinical Trial Agreements (CTAs) and other site contracts for CPM and Legal review.

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WAVSYS

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Construction Project Coordinator (REMOTE)

OR · Remote

$25 - $28/hr

COP Review & Submission: Own the intake, verification, and submission of Close-Out Packages (COPs ... Maintain project data integrity within T-Mobile systems. Perform data entry, record keeping, and ...

New

Project Sapiens

Renewal Operations Manager

OR · Remote

Remote - North America Position Summary: Sapiens is building a dedicated renewal function - and you ... Review contract data to understand pricing history, renewal dates, and structural opportunities ...

Logging-in

Principal Cloud Engineer

OR · Remote

$55 - $60/hr

Remote Duration: Long Term We are seeking a Principal Cloud Engineer who thrives at the ... Data flow and integration patterns. * Observability and operational runbooks. * Produce clear and ...

Ardent

Care Advisor I

Coos Bay, OR · Remote

Data & Feedback: Meticulously document all interactions in the CRM and track feedback to help our ... You are disciplined in a remote environment, detail-oriented, and able to manage multiple ...

Sapiens

Renewal Operations Manager

OR · On-site +1

Remote - North America Position Summary: Sapiens is building a dedicated renewal function - and you ... Review contract data to understand pricing history, renewal dates, and structural opportunities ...

Amgen, Inc.

Biostatistical Programming Senior Manager

OR · On-site +1

In this vital role you will ensure all statistical aspects pertaining to clinical activities meet ... Develop, review, and implement Policies, SOPs and other controlled documents affecting GSP globally.

Sapiens

Vice President of Sales, North America Life

OR · On-site +1

Remote The Vice President of Sales, North America (Life) will report directly to the Chief Revenue ... Implement data-driven sales methodologies, leveraging funnel metrics, forecasting, and analytics to ...

Hughes Marino

Senior Lease Auditor

OR · Remote

$85K - $105K/yr

... review of clients' legal documentation.Impeccable attention to detail and exacting standards for data accuracy, lease knowledge, and follow-up.Able to enthusiastically approach challenges and work ...

Hughes Marino

Senior Lease Auditor

OR · On-site +1

$85K - $105K/yr

Annual lease reconciliation reviews and lease audits for our lease administration clients ... Fully remote position. Hughes Marino is an equal opportunity employer.

EVIDENT

Director Digital Marketing

OR · On-site +1

... review and optimization decisions • Track channel contribution to pipeline and marketing ... You understand pipeline influence, conversion funnels, cohort analysis and you use data to make ...

Bausch+Lomb Companies Inc.

Director, Product Owner

OR · Remote

... and translate clinical and commercial data into clear, actionable recommendations for B+L ... US- Remote All qualified applicants will receive consideration for employment without regard to ...

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Remote Clinical Data Reviewer information

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How much do remote clinical data reviewer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for remote clinical data reviewer in Remote, OR is $26.22, according to ZipRecruiter salary data. Most workers in this role earn between $14.42 and $36.25 per hour, depending on experience, location, and employer.

What is a remote clinical data reviewer?

Remote Clinical Data Reviewers are professionals who analyze and validate clinical trial data from a remote location, ensuring its accuracy and compliance with regulatory standards. They play a crucial role in identifying discrepancies, data entry errors, and protocol deviations in clinical studies. By collaborating with study teams and using electronic data capture systems, they help maintain data integrity and support the successful completion of clinical research projects. This position allows for flexible work arrangements, as the tasks can be performed from home or any location with secure internet access.

What skills and qualifications are needed to be a remote clinical data reviewer?

To thrive as a Remote Clinical Data Reviewer, you need a strong background in life sciences or a related field, experience with clinical trial processes, and a keen eye for detail. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and knowledge of GCP (Good Clinical Practice) guidelines or relevant certifications are typically required. Strong analytical skills, effective written communication, and time management are important soft skills for success in this role. These skills ensure accurate data validation, regulatory compliance, and efficient remote collaboration to support high-quality clinical research outcomes.

What are common challenges faced by remote clinical data reviewers and how can they be managed?

Remote Clinical Data Reviewers often face challenges such as ensuring data accuracy across different electronic data capture systems, maintaining effective communication with on-site teams, and managing time zone differences. To manage these challenges, it’s important to establish clear protocols for data verification, utilize collaborative tools for real-time communication, and adhere to a structured workflow and regular check-ins with the broader project team. Proactively seeking clarification and staying updated with protocol amendments also help ensure high-quality data review from a remote setting.

What is the difference between Remote Clinical Data Reviewer vs Remote Clinical Data Coordinator?

AspectRemote Clinical Data ReviewerRemote Clinical Data Coordinator
CredentialsTypically requires a degree in life sciences, health informatics, or related field; certifications like CDISC or CDM are commonSimilar credentials; often holds degrees in health sciences or related fields; certifications may include clinical trial management
Work EnvironmentPrimarily reviews and validates clinical data, often working independently or in small teamsCoordinates data collection, manages databases, and communicates with sites and teams
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for data quality assuranceEmployed by similar organizations to oversee data flow and trial documentation

The main difference is that Remote Clinical Data Reviewers focus on analyzing and validating clinical data, while Remote Clinical Data Coordinators handle data management and coordination tasks. Both roles require similar educational backgrounds and are integral to clinical trial processes, but their daily responsibilities differ significantly.

What are popular job titles related to Remote Clinical Data Reviewer jobs in Remote, OR?

For Remote Clinical Data Reviewer jobs in Remote, OR, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Data Reviewer jobs in Remote, OR look for?

The top searched job categories for Remote Clinical Data Reviewer jobs in Remote, OR are:

What cities near Remote, OR are hiring for Remote Clinical Data Reviewer jobs?

Cities near Remote, OR with the most Remote Clinical Data Reviewer job openings:

Remote Clinical Data Reviewer jobs near you
Infographic showing various Remote Clinical Data Reviewer job openings in Remote, OR as of August 2026, with employment types broken down into 3% Internship, 59% Full Time, 15% Part Time, 4% Temporary, and 19% Contract. Highlights an 100% Remote job distribution, with an average salary of $54,530 per year, or $26.2 per hour.

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

IT ENGAGEMENTS INC

OR • Remote

$68 - $70/hr

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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