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Remote Clinical Data Entry 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 ...

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 ...

Data Classification Associate, Corporate

OR · On-site +1

$16 - $20.75/hr

Our data and research teams transform raw data into strategic intelligence, delivering accurate ... This is a remote-friendly opportunity that can sit in NYC (where our headquarters is located), one ...

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

Remote micro1 is engaging Computational Biology & Cheminformatics Experts to contribute their ... clinical data sources. * Provide expert insights on structure-activity and structure-property ...

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Remote Clinical Data Entry information

What is a remote clinical data entry?

A Remote Clinical Data Entry job involves inputting, managing, and updating clinical data in digital systems from a remote location. Professionals in this role ensure accuracy, confidentiality, and compliance with healthcare regulations. They may work with clinical trial data, patient records, or other medical information. Strong attention to detail, familiarity with medical terminology, and proficiency in data entry software are essential for success in this field.

What are the key skills and qualifications needed for remote clinical data entry?

To excel in Remote Clinical Data Entry, you need strong attention to detail, fast and accurate typing skills, and a familiarity with medical terminology, often supported by a diploma or coursework in health sciences or medical administration. Knowledge of clinical data management systems (such as EDC platforms), electronic health records (EHRs), and basic proficiency with spreadsheet software like Excel is typically required, and certification in data entry or health information management can be advantageous. Exceptional organizational skills, reliability, and the ability to work independently while maintaining clear communication with remote teams are standout soft skills for this role. These abilities ensure accurate, timely data handling, facilitate compliance with healthcare regulations, and contribute to the integrity of patient records and research data.

What does a typical workday look like for remote clinical data entry?

A typical workday in a remote clinical data entry position involves reviewing clinical documents and inputting critical data into electronic databases or health record systems. You will regularly communicate with healthcare professionals, study coordinators, or data managers to clarify details and ensure data accuracy. Most days require a balance between independent data entry tasks and virtual team meetings or status updates, all within strict privacy and compliance guidelines. The remote environment offers flexibility, but it also requires excellent self-management to meet deadlines and maintain high accuracy standards. Over time, this experience can open doors to roles in clinical data management, trial coordination, or health information analysis.

Are any remote clinical data entry jobs legit?

Remote clinical data entry jobs are legitimate positions that involve inputting and managing clinical trial data from home, often requiring attention to detail and familiarity with data management software. However, job seekers should verify the employer's credibility and be cautious of scams that request upfront payments or personal information. Conducting research on the company and reading reviews can help ensure the job's legitimacy.

What is clinical data entry?

Clinical data entry involves inputting and managing patient information, research data, or medical records into electronic databases or systems. It requires attention to detail, accuracy, and familiarity with healthcare terminology and data management tools. This role supports clinical trials, healthcare providers, and research organizations in maintaining precise and organized medical data.

What are the most commonly searched types of Clinical Data Entry jobs in Oregon?

The most popular types of Clinical Data Entry jobs in Oregon are:

What cities in Oregon are hiring for Remote Clinical Data Entry jobs?

Cities in Oregon with the most Remote Clinical Data Entry job openings:

Infographic showing various Remote Clinical Data Entry job openings in Oregon as of August 2026, with employment types broken down into 74% Full Time, 19% Part Time, and 7% Contract. Highlights an 100% Remote job distribution.

Senior Clinical Scientist, ECD

Natera

OR • On-site, Remote

Full-time

Re-posted 16 days ago


Natera rating

7.7

Company rating: 7.7 out of 10

Based on 38 frontline employees who took The Breakroom Quiz

56th 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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