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Senior Remote Clinical Data Abstractor Jobs in Oregon

San Carlos, CA or Remote, USA (West Coast or Mountain time zones preferred) PRIMARY ... Lead medical and clinical data review to ensure data quality and integrity * Analyze complex ...

Clinical Data Audit Consultant

OR · On-site +1

$33.71 - $60.67/hr

The Clinical Data and Audit Consultant is responsible for the clinical content component of all ... with remote, hybrid, field or office work schedules. Actual pay will be adjusted based on an ...

HSS has a proven history of placing talented healthcare professionals in clinical and non-clinical ... Assists Manager in training abstractor staff and participates in the medical record IRR. Identifies ...

Senior Data Analyst

OR · On-site +1

$90K - $125K/yr

What you'll do: * Develop clinical data models using dbt and SQL based on business need and ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Senior/Principal Data Engineer

OR · On-site +1

$125K - $172K/yr

Architect production-grade data pipelines that integrate clinical data through multiple channels ... Senior: 5+ years; Principal: 8+ years). * Expert-level proficiency in Python ( required ) and ...

Director, Clinical Science

OR · On-site +1

$79K - $108K/yr

Lead the development of trial execution timelines and deliver unvarnished study status updates to senior leadership * Lead rigorous clinical data review loops to interrogate datasets for specific ...

Senior AI Engineer, Real-World Data

OR · On-site +1

$122K - $161K/yr

Our RWD products transform unstructured and semi-structured clinical documents into structured ... This is a senior individual contributor role with high autonomy and end-to-end ownership from ...

Data integrity and analysis : Lead the review, interpretation, and quality control of clinical data ... Prepare and deliver high-impact presentations, proposals, and reports for senior leadership ...

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 ...

Senior Director, Biostatistics

OR · On-site +1

$290K/yr

Work collaboratively with Clinical Development, Clinical Operations, Clinical Data Managers ... Remote working environment with frequent in-person meetings to address complex problems and build ...

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Senior Remote Clinical Data Abstractor information

What is a senior remote clinical data abstractor?

A Senior Remote Clinical Data Abstractor is a healthcare professional responsible for reviewing medical records and extracting important clinical data for research, quality improvement, or regulatory compliance purposes. They work remotely, using secure digital platforms to access and abstract patient information according to specific guidelines and protocols. This role often requires advanced knowledge of medical terminology, coding systems, and healthcare data standards, as well as experience in clinical data abstraction. Senior positions also involve mentoring junior abstractors, ensuring data accuracy, and collaborating with clinical teams to support organizational goals.

What are the key skills and qualifications needed to thrive as a senior remote clinical data abstractor?

To thrive as a Senior Remote Clinical Data Abstractor, you need extensive clinical knowledge, strong analytical skills, and experience with medical terminology and healthcare documentation, often supported by a degree in nursing, HIM, or a related field. Proficiency with EHR systems, data abstraction software, and relevant certifications such as Certified Clinical Data Specialist (CCDS) are typically required. Attention to detail, self-motivation, and effective communication are soft skills that help you excel in a remote and highly regulated environment. These skills ensure accurate data collection and reporting, directly impacting patient outcomes and compliance with quality standards.

What are some common challenges faced by senior remote clinical data abstractors and how can they be addressed?

Senior Remote Clinical Data Abstractors often encounter challenges such as maintaining data accuracy when working with diverse electronic health records (EHR) systems and ensuring consistent communication with clinical teams. Addressing these challenges typically involves developing strong attention to detail, staying updated on the latest abstraction guidelines, and utilizing secure collaboration tools for effective remote teamwork. Regular training and participation in team meetings can also help abstractors stay aligned with evolving protocols and foster a supportive, solution-oriented environment.

What job categories do people searching Senior Remote Clinical Data Abstractor jobs in Oregon look for?

The top searched job categories for Senior Remote Clinical Data Abstractor jobs in Oregon are:

Infographic showing various Senior Remote Clinical Data Abstractor job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution.

Senior Clinical Scientist, ECD

OR • On-site, Remote


Natera
Biotechnology Research and Development • 1 - 5K employees

7.7

Company rating: 7.7 out of 10

Based on 38 frontline employees who took The Breakroom Quiz

57th of 120 rated laboratories

People enjoy working here

Good employer

Paid breaks


Full-time

Re-posted 25 days ago


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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