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Full Time Clinical Research Rater Jobs in Washington

Cape Fox SS

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

This rate represents the company's good faith and reasonable estimate of possible compensation at ... Supports clinical staff develop, implement and maintain clinical research data files and materials ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... This is a full-time, on-site role in Bethesda, MD. * Provide guidance and operational training to ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD

$65K - $108K/yr

We are seeking a Clinical Research Coordinator to provide comprehensive clinical research ... This is a full-time, on-site role in Bethesda, MD. * Provide guidance and operational training to ...

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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

Cape Fox Corporation

Bethesda, MD • On-site

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Job description

Job Title
Clinical Research Coordinator
Job Description
Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH.
The total hourly pay for this non-exempt position is $30.00 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn.
Supports clinical staff develop, implement and maintain clinical research data files and materials.
- Assist preparing and submitting for review accurate source documents related to all research procedures.
Collects research data and prepares information for inputs and analysis.
- Work with staff on data acquisition and analysis using a variety of methods, including recruitment, entry, management and display for
the Department of Bioethics research studies.
Supports the development of forms and questionnaires.
- Work with staff to coordinate the logistics of courses and workshops, including the course Ethical and Regulatory Aspects of Clinical Research, and the Empirical Research Lab.
Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
- Conduct literature searches; gather and synthesize background information.
Monitors subject's progress and reports adverse events.
- Assist staff writing progress reports and contributions to peer-reviewed scientific manuscripts.
Supports assembly, development and review of new research projects.
- Work with staff on manuscript preparation for research studies and manuscript submission.
- Prepare materials for IRB submission, manuscript transmittals and other necessary approvals and reviews.
Supports the creation and management of clinical websites and web-based tools.
- Collaborate with staff on the maintenance of Departmental metrics, databases and website.
Travel Requirements
0 - 10%
Job Requirements
Preferred Professional Experience:
Manuscript preparation - Data acquisition - Coordinating events - Protocol development - Statistical Analysis - Recruitment - Research
Familiarity with STATA and NVivo
Education and Certifications:
  1. Bachelor's Degree Required
  2. Two years of related experience

Core Skills:
  1. Strong organizational and time management skills.
  2. Excellent interpersonal and communication skills.
  3. Attention to detail in data collection and documentation.
  4. Proficiency in relevant computer applications and software.
  5. Ability to work both independently and collaboratively.
  6. Problem-solving and critical-thinking abilities.

Category
Science / Research
Location
Bethesda, MD - Bethesda, MD 20892 US (Primary)
Education
Bachelor's Degree

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