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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 ...

Ōura

Clinical Research Coordinator

$24.75 - $33/hr

We are looking for a Clinical Research Coordinator to join our Clinical Research Operations team ... This is a remote US role, with a preference for candidates based in San Francisco, Boston, or San ...

New

Danaher

Sr. Clinical Research Associate

The position will be fully remote within the United States. In this role, you will have the ... clinical research experience OR Doctoral degree in field with 0-2 years clinical research ...

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 ...

New

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 ...

IQVIA

Clinical Research Coordinator

Philadelphia, PA · Remote

$35 - $42/hr

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

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

As of Jul 12, 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 45% Full Time, 44% Part Time, and 11% Contract. Highlights an 100% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.
Senior Clinical Research Associate

Senior Clinical Research Associate

Cognitive Research Corporation

Remote

Full-time

Posted 4 days ago

New

Job description

The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Essential Duties & Responsibilities
  • Initiates, monitors, and closes-out investigative sites in accordance with FDA/ICH regulations.
  • Tracks and maintains study specific non-Case Report Form database
  • Administers Clinical research projects; collects investigator documentation, site management, clinical contact, and prepare reports as required
  • Ensures appropriate source document review and source document verification as required
  • Reviews Case Report Forms to identify erroneous, missing, or incomplete data
  • Generates queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly
  • Verifies study drug accountability; generates and tracks drug shipments and storage
  • Travels as necessary, based on project needs and according to Clinical Monitoring Plan requirements
  • Performs data collection, retrieval, entry and clean up as necessary
  • Develops and maintains strong relationships with Investigator(s) and site staff
  • Independently manages sites resulting in acceptable Quality Assurance reports.
  • Escalates study/site issues/deviations appropriately
  • Serves as lead monitor for a protocol or project by creating study files, arranges monitoring schedules, leads the project team, organize and run meetings and performs other project management duties as assigned by management
  • Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format
  • Reports, writes narratives, and follows-up on reported serious adverse events
  • Interacts and attends client meetings, as appropriate
  • Mentors junior staff/CRAs
  • Quality oversight checks of monitoring
  • Performs other duties as assigned

Qualifications
  • Bachelor's degree, or RN, in a related field or equivalent combination of education, training and experience
  • Minimum 5 years' experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
  • Ability to work and travel independently with minimal supervision
  • Experience with numerous EDC systems.
  • Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Office, Zoom and Adobe
  • Excellent writing and verbal skills, English language proficiency
  • Meticulous attention to detail
  • Time management and ability to prioritize tasks
  • Ability to travel up to 70%

Department Clinical Operations Role Senior Clinical Research Associate Locations Remote, US Remote status Fully Remote Employment type Full-time

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