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Remote Clinical Scientist Jobs in Oregon (NOW HIRING)

San Carlos, CA or Remote, USA (West Coast or Mountain time zones preferred) PRIMARY ... Own day-to-day clinical science responsibilities across assigned studies * Drive resolution of ...

Clinical Scientist - Respiratory Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical ...

Clinical Scientist - Oncology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs ...

Clinical Scientist - Ophthalmology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical ...

Clinical Scientist - Cardiovascular Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical ...

Data Scientist

OR · On-site +1

As a Data Scientist at BetterHelp, you'll join a diverse team of licensed clinicians, engineers ... Remote work with regular in-person bonding experiences sponsored by the company * Competitive ...

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Remote Clinical Scientist information

See Oregon salary details

$29

$57

$86

How much do remote clinical scientist jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for remote clinical scientist in Oregon is $57.89, according to ZipRecruiter salary data. Most workers in this role earn between $42.45 and $72.16 per hour, depending on experience, location, and employer.

What is a remote clinical scientist?

A Remote Clinical Scientist conducts clinical research, analyzes data, and supports drug or therapy development while working remotely. They collaborate with cross-functional teams, including medical, regulatory, and biostatistics professionals, to ensure study integrity and compliance. Responsibilities may include protocol development, clinical trial monitoring, and scientific data interpretation. This role typically requires expertise in clinical research, regulatory guidelines, and therapeutic areas relevant to the employer’s focus. It allows professionals to contribute to clinical advancements without being tied to a physical location.

How does a remote clinical scientist collaborate with onsite teams and manage project responsibilities from a distance?

Remote Clinical Scientists work closely with clinical research associates, data managers, and investigators through frequent virtual meetings, collaborative platforms, and electronic documentation tools. They are responsible for reviewing data, monitoring trial progress, ensuring protocol compliance, and addressing site queries, all while maintaining regular communication with onsite staff. This remote setup requires proactive scheduling, timely reporting, and strong organizational skills to stay aligned with project milestones. The ability to leverage digital communication tools ensures effective teamwork and consistent project oversight despite physical distance.

What are the key skills and qualifications needed to thrive in the remote clinical scientist position, and why are they important?

To excel as a Remote Clinical Scientist, you typically need an advanced degree in a life science field, experience in clinical research, and strong data analysis skills. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and regulatory requirements such as GCP is crucial, as are relevant certifications like SOCRA or ACRP. Excellent communication, self-motivation, and problem-solving abilities set apart top candidates in this remote role. These skills ensure the effective oversight of clinical trials, compliance with regulations, and successful remote collaboration with multidisciplinary teams.

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

The most popular types of Clinical Scientist jobs in Oregon are:

What are popular job titles related to Remote Clinical Scientist jobs in Oregon?

For Remote Clinical Scientist jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Remote Clinical Scientist jobs?

Cities in Oregon with the most Remote Clinical Scientist job openings:

Infographic showing various Remote Clinical Scientist job openings in Oregon as of August 2026, with employment types broken down into 72% Full Time, 22% Part Time, and 6% Contract. Highlights an 6% Hybrid, and 94% Remote job distribution, with an average salary of $120,401 per year, or $57.9 per hour.

Senior Clinical Scientist, ECD

Natera

OR • On-site, Remote

Full-time

Re-posted 9 days ago


Key responsibilities

  • Lead the execution of clinical studies, including study design, protocol development, and study document review.

  • Conduct medical and clinical data review to ensure data quality, analyze datasets for trends and risks, and translate findings into insights.

  • Manage day-to-day clinical science responsibilities, address operational challenges, and collaborate with cross-functional teams to monitor study progress and performance.


Natera rating

7.8

Company rating: 7.8 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

56th of 121 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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