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Remote Clinical Data Reviewer Jobs in Oregon (NOW HIRING)

... data review, and cross-functional problem solving while contributing to broader clinical development discussions and strategy. Location: San Carlos, CA or Remote, USA (West Coast or Mountain time ...

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Serve as the technical escalation authority for complex data infrastructure and clinical data pipeline issues. * Complete all responsibilities as outlined in the annual performance review and/or goal ...

CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

Performing data review and resolution of queries to maintain high-quality clinical data ... MM2 #LI-Remote Employment with ICON is contingent upon having the legal right to work in the ...

Data Scientist

$96K - $134K/yr

Remote Department: Clinical and Population Health Analytics Schedule: Full-time | Day shift Salary ... Work alongside senior data scientists and clinical mentors to translate broad clinical questions ...

Contractor Location: Remote micro1 is engaging Bioinformatics Scientists to contribute their ... Evaluate and synthesize findings from biological, chemical, and clinical data sources. * Offer ...

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Remote Clinical Data Reviewer information

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 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 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 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 popular job titles related to Remote Clinical Data Reviewer jobs in Oregon? For Remote Clinical Data Reviewer jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Remote Clinical Data Reviewer jobs in Oregon look for? The top searched job categories for Remote Clinical Data Reviewer jobs in Oregon are:
What cities in Oregon are hiring for Remote Clinical Data Reviewer jobs? Cities in Oregon with the most Remote Clinical Data Reviewer job openings:

Senior Clinical Scientist, ECD

Natera

OR • On-site, Remote

Other

Re-posted 7 days ago


Natera rating

7.6

Company rating: 7.6 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories


Job description

POSITION SUMMARY: 

We are seeking a Senior Clinical Scientist to lead execution of key components of clinical development for our early cancer detection (ECD) program. This role is central to leading study execution, clinical data review, study design, and generation of scientific insights across multiple studies. The successful candidate will contribute meaningfully to clinical development strategy through hands-on study leadership, cross-functional execution, and data-driven decision-making. 

You will serve as a clinical science lead within cross-functional teams-partnering closely with Clinical Operations, Biostatistics, Medical Affairs, and Regulatory to drive study execution, identify risks and opportunities, and contribute to clinical development strategy through study-level leadership and scientific insight.

This role is best suited for a clinical scientist who enjoys remaining closely involved in study execution, clinical data review, and cross-functional problem solving while contributing to broader clinical development discussions and strategy.

Location: San Carlos, CA or Remote, USA (West Coast or Mountain time zones preferred)

PRIMARY RESPONSIBILITIES: 

Lead Clinical Development & Study Design

  • Lead substantial aspects of ECD clinical studies or multiple studies
  • Drive study design, including objectives, endpoints, eligibility criteria, and schedules of assessments
  • Author and review protocols, ICFs, CRFs, and study documents
  • Contribute meaningfully to clinical development strategy and study-level decision-making
  • Contribute to process improvements and development of best practices

Drive Data Review & Strategic Insight

  • Lead medical and clinical data review to ensure data quality and integrity
  • Analyze complex datasets to identify trends, risks, and opportunities
  • Translate data into actionable insights that inform study and program decisions
  • Partner with safety and medical teams on signal detection and escalation

Lead Cross-Functional Execution

  • Own day-to-day clinical science responsibilities across assigned studies
  • Drive resolution of study-level issues, risks, and operational challenges
  • Partner closely with Clinical Operations, Medical Affairs, Regulatory, and Biostatistics to monitor study conduct, data quality, enrollment performance, and milestone delivery
  • Make study-level decisions and recommendations in ambiguous situations with limited oversight
  • Represent Clinical Science in internal and external forums (e.g., investigators, KOLs)

Drive Study Performance & Program Value

  • Prioritize activities across studies to ensure quality, timelines, and program impact
  • Actively monitor study conduct, enrollment performance, protocol compliance, and clinical data quality across studies
  • Identify operational risks early and implement corrective actions to maintain study timelines and quality

Advance Scientific Communication

  • Lead development of abstracts, presentations, and manuscripts
  • Translate clinical and statistical results into clear scientific narratives
  • Support internal decision-making and external evidence generation

QUALIFICATIONS: 

  • Advanced degree (PhD, PharmD, MD, or equivalent; MS, MPH, RN with experience considered)
  • 6+ years of experience in clinical research, clinical science, or related field
  • Strong experience leading clinical studies and contributing to study design
  • Demonstrated experience leading and executing clinical studies, including clinical data review, study-level decision making, issue management, and cross-functional coordination

Preferred Qualifications: 

  • Experience in oncology, diagnostics, or early cancer detection
  • Experience working across multiple studies or programs
  • Track record of scientific publications and conference presentations

KNOWLEDGE, SKILLS, AND ABILITIES: 

  • Ability to lead complex clinical studies or multiple workstreams independently
  • Ability to balance scientific rigor with pragmatic decision-making in a fast-paced environment
  • Demonstrated ownership mindset with willingness to operate outside traditional functional boundaries when needed to advance study and program goals
  • Strong analytical skills with ability to synthesize complex data into decisions
  • Effective influencer across functions and senior stakeholders
  • Excellent scientific communication skills



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