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Full Time Clinical Research Rater Jobs in Washington

Cape Fox Corporation

Research Nurse

Bethesda, MD · On-site

$56/hr

This rate represents the company's good faith and reasonable estimate of possible compensation at ... Work with staff to develop procedure manuals for clinical research protocols. * Work with staff to ...

Cape Fox SS

Research Nurse

Bethesda, MD

$56/hr

The total hourly pay for this exempt position is $56.00 for up to 40 hours per week This rate ... Work with staff to develop procedure manuals for clinical research protocols. Work with staff to ...

Guidehouse

Research Nurse

Rockville, MD

$98K - $163K/yr

This is a full-time, on-site opportunity in Rockville, MD. * Monitor integrity, completeness and ... Participate in clinical practice and research support meetings and develop multidisciplinary ...

Guidehouse

Research Nurse

Rockville, MD · On-site

$98K - $163K/yr

This is a full-time, on-site opportunity in Rockville, MD. * Monitor integrity, completeness and ... Participate in clinical practice and research support meetings and develop multidisciplinary ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$74K - $124K/yr

This is a full-time opportunity located in Bethesda, MD. * Work with a diverse clinical research team including physicians, advanced practice providers, patient care coordinators, protocol navigators ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$98K - $163K/yr

This is a full-time opportunity located in Bethesda, MD. * Work with a diverse clinical research team including physicians, advanced practice providers, patient care coordinators, protocol navigators ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$98K - $163K/yr

This is a full-time opportunity located in Bethesda, MD. * Work with a diverse clinical research team including physicians, advanced practice providers, patient care coordinators, protocol navigators ...

Guidehouse

Research Nurse Specialist

Bethesda, MD · On-site

$74K - $124K/yr

This is a full-time opportunity located in Bethesda, MD. * Work with a diverse clinical research team including physicians, advanced practice providers, patient care coordinators, protocol navigators ...

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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.

What are popular job titles related to Full Time Clinical Research Rater jobs in Washington?

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 Coordinator GW- Washington DC

The US Oncology Network

Beltsville, MD • On-site

$51K - $88K/yr

Full-time

Re-posted 13 days ago

US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

378th of 898 rated healthcare providers

Job description

Overview
Join Our Team at Maryland Oncology Hematology!
We're looking for passionate and talented professionals to join our team in providing exceptional cancer care. If you're dedicated to making a difference for patients, physicians, and colleagues, we want to hear from you! With 15+ locations across Maryland and DC, we offer a dynamic and supportive environment where you can grow and thrive.
Explore opportunities with us and apply today!
The general pay scale for this position at MOH is $51,545 - $88,987 per year. The actual hiring rate is dependent on many factors, including but not limited to prior work experience, education, job/position responsibilities, location, work performance, etc.
Responsible for supporting the management and coordination of tasks for multiple clinical research studies to include screening patients for eligibility and participates in the subject's study visits and required activities per protocol. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers, and participation in required training and education, Assures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.
This role will be located at GW Medical Faculty Associates, 2150 Pennsylvania Avenue, NW, Washington, DC 20037
Responsibilities
Key Responsibilities
  • Screens potential participants for protocol eligibility. Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials.
  • Coordinates participant care in compliance with protocol requirements. May disburse investigational product and maintain accountability records. Oversees preparation of orders by providers to ensure protocol compliance. Packages and ships laboratory specimens to central vendors as applicable. Completion of Hazmat and/or IATA training may be required.
  • In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment. Thoroughly documents all findings and participates in data collection.
  • Prepares study-related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports.
  • Maintains regulatory documents in accordance with organizational SOPs and applicable regulations. May assist with scheduling monitoring and auditing visits, and interact with monitors/auditors as needed. May collaborate with research leadership in study selection processes.
  • Participates in required training and education programs. May contribute to education of clinical staff regarding research procedures. Works with staff to develop action plans and performance improvement initiatives to enhance quality.
  • May compile and report protocol activity, enrollment trends, data entry compliance, and research financial information to practice leadership and providers. May review protocol-specific billing guides and submit billing information to the appropriate personnel.

Qualifications
Minimum Job Qualifications (Knowledge, Skills & Abilities)
Education/Training
  • Associate's degree in a clinical or scientific discipline required; Bachelor's degree preferred.
  • Minimum three years of experience in a clinical or scientific field required.
  • SoCRA or ACRP certification preferred.

Business Experience
  • Experience with Microsoft Office applications.
  • Experience working with physicians preferred.
  • Experience in clinical research preferred.

Specialized Knowledge/Skills
  • Excellent communication skills.
  • Strong organizational abilities.
  • Ability to multi-task effectively.
  • Strong time-management skills.
  • High level of interpersonal skills to interact with individuals at various levels.
  • Strong attention to detail.
  • Ability to work in a fast-paced environment.
  • May be responsible for basic clinical assessments.

Working Conditions
Environment
  • Traditional office and clinical environment.
  • The work environment characteristics described here represent those an employee may encounter while performing essential job functions. Reasonable accommodations will be provided as needed.
  • Exposure to communicable diseases, toxic substances, medical preparations, and other conditions common to a clinical research environment.

Physical Requirements
  • Significant amount of computer-based work required.
  • Requires standing and walking for extended periods.
  • Occasionally lifts and carries items up to 40 lbs.
  • Requires corrected vision and hearing within normal range.
  • Reasonable accommodations will be provided to enable individuals with disabilities to perform essential functions.

This description is general in nature and is not intended to list every responsibility. Other duties may be assigned as needed to meet organizational goals.

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