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Clinical Research Rater Remote Jobs (NOW HIRING)

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

Essentia Health

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

Experience in oncology, clinical research, academic research or similar area. Over 1 year computer ... None FTE: 1 Possible Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America ...

Hanger, Inc.

Director of Clinical Research

$140K - $150K/yr

The Director of Clinical Research will serve within Hanger's Department of Clinical and Scientific ... Remote: Pay range of $140,000- $150,000 + bonus + benefits. This pay range is posted to comply with ...

Aptive

Clinical Research Protocol Specialist

Job Summary Aptive Resources is seeking a Clinical Research Protocol Manager to support the ... This is a full-time (40 hours/week), 100% remote position. This position is currently funded ...

Aptive

Clinical Research Protocol Specialist

Job Summary Aptive Resources is seeking a Clinical Research Protocol Manager to support the ... This is a full-time (40 hours/week), 100% remote position. This position is currently funded ...

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How much do clinical research rater remote jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for clinical research rater remote in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a Clinical Research Rater (Remote)?

A Clinical Research Rater (Remote) is a professional who works from a remote location to assess and evaluate participants in clinical research studies. They are responsible for administering psychological or cognitive assessments, interviews, and questionnaires to study subjects according to research protocols. The data they collect is used to determine the effectiveness and safety of medical treatments or interventions being studied. This position requires strong attention to detail, excellent communication skills, and the ability to follow standardized procedures. Remote raters typically collaborate with research teams via secure digital platforms and may require specific certifications or training.

What are the key skills and qualifications needed to thrive as a Clinical Research Rater (Remote), and why are they important?

To thrive as a Clinical Research Rater (Remote), you need a background in psychology, neuroscience, or a related field, along with experience in clinical research and administering standardized assessments. Familiarity with electronic data capture (EDC) systems, clinical trial protocols, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, strong organizational skills, and the ability to communicate clearly with research teams are crucial soft skills. These abilities ensure accurate data collection, adherence to study protocols, and high-quality research outcomes in a remote environment.

What are some typical challenges faced by remote Clinical Research Raters, and how can they be addressed?

Remote Clinical Research Raters often face challenges such as maintaining consistent communication with study teams and ensuring accurate, unbiased assessments when working independently. To address these, it's important to establish clear protocols for virtual collaboration, regularly attend team meetings, and utilize secure data management systems. Staying organized and proactively reaching out for clarification when needed can help maintain high-quality data collection and foster a supportive remote work environment.

What is the difference between Clinical Research Rater Remote vs Clinical Data Entry Specialist?

AspectClinical Research Rater RemoteClinical Data Entry Specialist
Required credentialsHigh school diploma or equivalent; some roles may require clinical or research experienceHigh school diploma or equivalent; data entry skills preferred
Work environmentRemote, flexible hours, often part-timeRemote or on-site, regular hours, often full-time
Employer and industry usagePharmaceutical companies, research organizations, clinical trial sitesHealthcare providers, research organizations, hospitals

While both roles involve working remotely in the healthcare and research industry, Clinical Research Rater Remote focuses on evaluating patient data and clinical outcomes, whereas Clinical Data Entry Specialists primarily input and manage clinical data. The roles differ in responsibilities, with the former emphasizing assessment and analysis, and the latter concentrating on data accuracy and entry.

More about Clinical Research Rater Remote jobs
What cities are hiring for Clinical Research Rater Remote jobs? Cities with the most Clinical Research Rater Remote job openings:
What are the most commonly searched types of Clinical Research Rater jobs? The most popular types of Clinical Research Rater jobs are:
What states have the most Clinical Research Rater Remote jobs? States with the most job openings for Clinical Research Rater Remote jobs include:
What job categories do people searching Clinical Research Rater Remote jobs look for? The top searched job categories for Clinical Research Rater Remote jobs are:
Clinical Research Rater Remote jobs near you
Infographic showing various Clinical Research Rater Remote job openings in the United States as of July 2026, with employment types broken down into 76% Full Time, 20% Part Time, 2% Temporary, and 2% Contract. Highlights an 100% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago

Job description

This is a remote position.

Position Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support the coordination and administration of clinical research studies while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process.

This position is ideal for someone with excellent organizational skills, strong attention to detail, and an interest in contributing to clinical research in a remote environment.

Essential Responsibilities
  • Assist with the day-to-day management of assigned clinical studies.
  • Maintain investigator site files, regulatory binders, and essential study documents.
  • Prepare, review, and file research documentation in accordance with study requirements.
  • Support participant scheduling and study visit coordination.
  • Enter, verify, and reconcile clinical data within electronic research systems.
  • Monitor study timelines and assist with tracking project deliverables.
  • Communicate effectively with investigators, sponsors, study participants, and internal research teams.
  • Identify and escalate documentation discrepancies or protocol deviations when appropriate.
  • Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements.
  • Perform additional administrative and research support duties as assigned.


RequirementsQualifications
Required
  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related discipline, or equivalent healthcare experience.
  • Strong organizational and problem-solving abilities.
  • Excellent verbal and written communication skills.
  • High level of accuracy and attention to detail.
  • Proficiency with Microsoft Office and web-based software applications.
  • Ability to manage multiple priorities while working independently in a remote setting.
Preferred
  • Previous experience supporting clinical research or healthcare operations.
  • Familiarity with ICH-GCP guidelines and FDA regulations.
  • Experience using Electronic Data Capture (EDC), CTMS, or eTMF systems.
  • Knowledge of clinical trial documentation and research workflows.
Work Schedule
  • Full-time
  • Monday through Friday
  • Standard business hours


BenefitsBenefits
  • Competitive salary
  • Comprehensive medical, dental, and vision coverage
  • 401(k) with employer contribution
  • Paid time off and company holidays
  • Remote work environment
  • Professional development and career advancement opportunities