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Full Time Clinical Research Rater Jobs in Virginia

Culmen International LLC

Clinical Protocol Developer

Portsmouth, VA · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

This position will support the Department Head of CID and is accountable for research related ... rate (including same or opposite sex domestic partners) * 401k - Vested immediately and 4% match

Culmen International LLC

Clinical Protocol Developer

Portsmouth, VA · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

This position will support the Department Head of CID and is accountable for research related ... rate (including same or opposite sex domestic partners) * 401k - Vested immediately and 4% match

The US Oncology Network

Research Assistant

Fairfax, VA · On-site

$19 - $26.25/hr

... Full Time Research Assistant for our Fairfax office. Under direct supervision, initiates and/or maintains accurate and current logs of all patients referred for participation in clinical research.

The US Oncology Network

Research Assistant

Fairfax, VA · On-site

$19 - $26.25/hr

... Full Time Research Assistant for our Fairfax office. Under direct supervision, initiates and/or maintains accurate and current logs of all patients referred for participation in clinical research.

Alcanza Clinical Research

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

Virginia Tech

Research Scientist

Blacksburg, VA

Research / Scientific A full-time research scientist is sought for the lab of Dr. Jenny Munson at ... This translational study will utilize patient tissues in established pre-clinical in vitro model ...

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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

Clincal Research Coordinator II/III

Arizona Arthritis & Rheumatology Associates

Fairfax, VA • On-site

$67K - $82K/yr

Full-time

Re-posted 12 days ago

Job description

Job Type
Full-time
Description
POSITION DESCRIPTION: The Clinical Research Coordinator II (CRC) reports to the Regional Research Manager and is responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs. The CRC collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability.
RESPONSIBILITIES:
  • Responsible for the coordination of observational and interventional clinical research trials assigned
  • Performance expectations will be assigned based on effort for each visit
  • Knowledge of all active protocols and disease indications within the company, and providing information about these protocols to staff and patients.
  • Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources.
  • The CRC is responsible for meeting recruitment goals for each study. The methodology of recruitment will include, but is not limited to daily chart review, hosting recruitment breakfasts, advertising when funds are available, referrals from rheumatologists and other AARA staff and may include attending health fairs and community outreach.
  • Keeping the clinical trial management system updated with newly recruited subjects, tracking completed visits and stipends for the participants and investigators, and ensuring status of each patient is accurate.
  • Responsible for chain of custody and accurate accountability of investigation product and devices.
  • Plans, prepares and performs tasks required by protocol, which may include, but not limited to the following:
  • Informed Consent
  • Obtaining patient medical history and medication lists
  • Phlebotomy and basic laboratory tests
  • Processing & shipping labs for central and local labs
  • Patient education and training
  • ECG
  • Administer questionnaires and assessments
  • Vital signs
  • Collect information for adverse event reporting
  • Assist with joint counts and other efficacy assessments
  • Data Entry and Query Resolution
  • Study drug administration, including injections
  • Tracking study supply inventory and reordering when necessary
  • Schedule patient visits in appropriate electronic systems
  • Documenting all patient visits and communications in progress notes
  • Triages adverse events and communicates with the research physician regarding the occurrence of adverse events and serious adverse events within 24 hrs. Follow-up with the subject and collect required information.
  • Provides educational information to subjects. Serves as a resource and support person for subjects and families by being a consistent person they can contact within the clinical research program.
  • Ensures uniform implementation of protocols by completing required training documentation in a consistent, accurate and timely manner.
  • Assists in regulatory functions, including but not limited to preparing appropriate Institutional Review Board (IRB) forms, processing updated informed consents, protocols, correspondence, and regulatory filing in an accurate and timely manner.
  • Responsible for administrative duties including filing documents related to subjects' participation in research, regulatory, lab results, receipts, invoices, calibration reports, etc.
  • Serves as a liaison to all physicians, employees, and third-party vendors.
  • Participates in monitoring visits from sponsor provided appointees, ensures monitors can meet/speak with PI and ensures all concerns are addressed in a timely manner.
  • Ensure the delegation logs are correct and only delegated site staff are performing duties as listed on the delegation log for any given study.
  • Ensures that primary referring physicians receive timely progress notes on the patient's diagnosis and treatment.
  • May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
  • Performs all functions according to established policies, procedures (SOPS), regulatory and accreditation requirements, federal and state regulations, good clinical practice, as well as applicable professional standards.
  • Provides all employees and research subjects with excellent service experience by consistently demonstrating professional decorum.
  • Maintaining office supply inventory while keeping an organized office space.
  • Travel as necessary for meetings and to assist other sites.

Requirements
Qualifications:
  • Bachelor's degree or equivalent
  • 1 year experience as a clinical research coordinator
  • Must have in-depth knowledge of medical procedures and clinical terminology
  • Possess strong organization and communication skills
  • Ability to develop and maintain strong professional relationships with all providers and research subjects
  • Excellent working knowledge of clinical research industry, ICH-GCP Guidelines and all federal regulations regarding clinical research.
  • Ability to lift 20 pounds
  • Willing and able to travel as needed to Rockville, White Oak and Frederick sites

Salary Description
67,000-82,744

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