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Full Time Clinical Research Rater Jobs in Virginia

Virginia Heart

Clinical Research Coordinator

Falls Church, VA

$25.75 - $34.50/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Fairfax, VAStatus: Full-Time/Non-Exempt Salary Range: $30.00 - $38.00 * No Evenings * No Nights ... The Clinical Research Coordinator will work in office at the Loudoun Office location ( upon ...

Alcanza

Clinical Research Site Manager

Fredericksburg, VA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations ... guidelines. * Full-time employees regularly scheduled to work at least 30 hours per week are ...

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Full Time Clinical Research Rater information

Is a full time clinical research rater a good career?

A full-time clinical research rater is a role that involves evaluating clinical trial data, often requiring attention to detail and knowledge of medical terminology. It can offer stable employment and opportunities for growth in the healthcare and research industries, especially for those with relevant backgrounds or certifications. However, job satisfaction depends on individual interests and career goals in the clinical research field.

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 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 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 most commonly searched types of Clinical Research Rater jobs in Virginia?

The most popular types of Clinical Research Rater jobs in Virginia are:

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

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

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

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

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

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

Full Time Clinical Research Rater jobs near you

Clinical Research Coordinator

The US Oncology Network

Salem, VA • On-site

$19.62 - $30.18/hr

Full-time

Re-posted 21 days ago

US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

381st of 887 rated healthcare providers

Job description

Overview
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.
Responsibilities
  • Screens potential patients for protocol eligibility.
  • Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials.
  • Assists with patient care in compliance with protocol requirements.
  • May disburse investigational drug and maintain investigational drug accountability.
  • Participates in data collection, entry, and reporting for the subjects.
  • In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
  • Participates in required training and education programs as well as monitoring and auditing activities.
  • May work directly with sponsors. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite.
  • Assists with collection and maintenance of regulatory documents in accordance with USOR SOPs and applicable regulations.
  • May assist in the packing and shipping of lab specimens to central vendors. May be required to complete Hazmat and/or IATA training.

Qualifications
Associate's degree in a clinical or scientific related discipline required, bachelor's degree preferred. Minimum one year of experience in a clinical or scientific related discipline, preferably in oncology required. Business Experience in Microsoft Office Experience working with physicians preferred Specialized Knowledge/Skills Must have excellent communication skills Excellent organizational skills Strong ability to multi-task Excellent time management skills Must have strong interpersonal skills to be able to interact with multiple people on many different levels Must have a high level of attention to detail Must be able to work in a fast-paced environment May be responsible for basic clinical assessments
Working Conditions: Environment (Office, warehouse, etc.) Traditional office environment. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment.
Physical Requirements (Lifting, standing, etc.) Large percent of time performing computer-based work is required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.
Salary Scale: The general pay scale for this position at BRCC is $19.62 - $30.18. 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.

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