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Full Time Clinical Research Rater Jobs in Washington

CBH Health

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ... Organizes research information for clinical trials. * Observes subjects and assists with data ...

CBH Health

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ... Organizes research information for clinical trials. * Observes subjects and assists with data ...

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ... Organizes research information for clinical trials. * Observes subjects and assists with data ...

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

... full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD ... Organizes research information for clinical trials. * Observes subjects and assists with data ...

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Full Time Clinical Research Rater information

What is a full time clinical research rater?

Full Time Clinical Research Raters are professionals who assess and document the progress, symptoms, and responses of patients participating in clinical research studies. They use standardized rating scales, interviews, and questionnaires to collect accurate data that helps determine the effectiveness and safety of new treatments or interventions. These raters play a vital role in ensuring the integrity and quality of clinical trial data, often working closely with clinicians, researchers, and study coordinators. Their responsibilities also include adhering to study protocols, maintaining patient confidentiality, and ensuring compliance with regulatory standards.

What are the key skills and qualifications needed to thrive as a full time clinical research rater?

Success as a Full Time Clinical Research Rater requires a background in psychology, neuroscience, or a related field, along with experience in clinical assessments and data collection. Familiarity with standardized rating scales, clinical trial databases, and regulatory compliance systems like Good Clinical Practice (GCP) certification is typically expected. Strong attention to detail, interpersonal communication, and objective judgment are crucial soft skills for accurate participant evaluation and collaboration with research teams. These competencies ensure reliable data collection, regulatory adherence, and the integrity of clinical research outcomes.

What are some typical challenges a full time clinical research rater may encounter, and how can they be managed?

Full Time Clinical Research Raters often face challenges such as managing large volumes of patient assessments, maintaining objectivity during subjective ratings, and adhering to strict study protocols. Balancing accuracy with efficiency is key, especially when dealing with sensitive patient information and tight study timelines. Collaborating closely with investigators and other research staff, participating in regular trainings, and using standardized rating tools can help ensure consistency and reliability in data collection.

What is the difference between Full Time Clinical Research Rater vs Part Time Clinical Research Rater?

AspectFull Time Clinical Research RaterPart Time Clinical Research Rater
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CertificationsOften requires relevant healthcare or research certificationsMay require similar certifications but less emphasis
Work EnvironmentFull-time employment in research facilities or remotePart-time roles, flexible locations
Employer UsageMajor research organizations, pharmaceutical companiesFreelance or contract research organizations

The main difference between a Full Time Clinical Research Rater and a Part Time Clinical Research Rater lies in work hours, certification emphasis, and employment type. Full-time roles offer consistent hours and benefits, while part-time positions provide flexibility. Both roles involve evaluating clinical data, but full-time positions are more integrated into research teams.

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For Full Time Clinical Research Rater jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Full Time Clinical Research Rater jobs in Washington look for?

The top searched job categories for Full Time Clinical Research Rater jobs in Washington are:

What cities in Washington are hiring for Full Time Clinical Research Rater jobs?

Cities in Washington with the most Full Time Clinical Research Rater job openings:

Full Time Clinical Research Rater jobs near you
Infographic showing various Full Time Clinical Research Rater job openings in Washington as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution.

Clinical Research Sub-Investigator (MD)

RE:Cognition Health, Inc

Fairfax, VA • On-site

Full-time

Re-posted 8 days ago

Job description

Company Description

Re:Cognition Health is a pioneering brain and mind clinic.

We specialize in the treatment and care of people showing symptoms of cognitive impairment or mental health concerns.  Using the latest progressive medical research and evidence based treatments we are passionate about transforming and optimising cognitive performance through education, clinical excellence and by providing access to emerging treatments.The Re:Cognition Clinics are major centers for international trials of disease-modifying and new symptomatic drugs for Alzheimer's disease and other neurological conditions.

Join a team that is a Global leader in clinical trials and dedicated to providing World-class Medical Care

Job Description

Unique opportunity to join a fast growing clinical trial research team in the field of cognitive impairment as a Sub-Investigator.  This is a full-time, regular position, working in the clinic from 9:00 to 5:30 pm Monday - Friday, with occasional hours outside this time frame to meet participant needs. You will work with a cutting-edge team dedicated to ensuring the future is better. 

Responsibilities include:

  • Complete of training on specific rating scales prior to the commencement of any study procedures
  • Perform clinical safety assessments and monitoring for study trial participation to include such items as: physical exams, EKG's, phlebotomy and lab work evaluation
  • Administer study drug(s), per protocol including placing and monitoring IV infusions
  • Perform lumbar punctures per the direction of the protocol and Principal Investigator
  • Recruit clinical protocol participants
  • Apply knowledge of center's clinical protocols for the care of study participants

The ideal individual is a dedicated clinical practitioner with experience in cognitive disease and clinical research.  This is a role that requires an individual who is capable and willing to perform both clinical and research related duties.  This position is an intricate research team, must be self-directed and have the ability to interact with multi discipline team and while maintaining the safety of the study participants and their families.

Qualifications

MD or Foreign Trained Medical Doctor, with current license to practice in Virginia

Current CPR Certification

Ability to follow HIPPA regulations in regards to patient confidentiality

Ability to pass a Background Check Investigation including Drug Screen

Additional Information

All your information will be kept confidential according to EEO guidelines.

https://www.recognition.health/

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