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Full Time Clinical Research Rater Jobs in Virginia

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 ...

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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 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 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:

Oncology Clinical Research Nurse/Coordinator

The US Oncology Network

Norfolk, VA

$47K - $128K/yr

Full-time

Life, Retirement

Re-posted 13 days ago


Key responsibilities

  • Present trial concepts, objectives, and treatment details to potential patients and conduct assessments to determine eligibility.

  • Participate in the informed consent process, enroll patients on protocol, and coordinate patient care in compliance with protocol requirements.

  • Collect and maintain regulatory documents, participate in scheduling monitoring and auditing visits, and interact with monitors and auditors.


US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

379th of 898 rated healthcare providers


Job description

Overview

Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research RN to support our office in Norfolk.

Employment Type: Full Time 

Hybrid

Benefits: M/D/V, Life Ins., 401(k) 

Compensation Range: $47,964.80 - $128,939.20. Actual pay is determined based on job-related factors such as relevant experience, education, credentials, skills, internal equity, and business needs. 


Responsibilities
  • Present trial concepts, objectives and treatment details to potential patients for various cellular therapy trials, while conducting detailed assessment and screening to determine their eligibility.
  • Participating in the informed consent process and enrolling patients on protocol
  • 80% of the job will be computer based, and direct patient care is limited in a non-RN Clinical Research Coordinator role
  • Collects and maintains regulatory documents in accordance with USOR SOP and applicable regulations. Participates in scheduling monitoring and auditing visits, as well as interacting with the monitors/auditors while onsite.
  • Coordinating patient care in compliance with protocol requirements
  • Collaborating with the physician to review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to drug study and thoroughly documenting all findings
  • Working directly with other research bases and/or sponsors
  • Overseeing the preparation of orders by physicians to assure that protocol compliance is maintained
  • Communicating with physicians regarding study requirements, need for dose modification and adverse event reporting

Qualifications
  • Experience in clinical research preferred
  • Experience with computer data entry and database management
  • Excellent written and oral communication skills
  • Ability to read, analyze, and interpret technical procedures such as protocols, informed consent, and regulatory documents
  • Graduate from an accredited program for nursing education (BSN preferred)
  • Minimum of one (1) year nursing experience, preferably in oncology
  • Current licensure as an RN in Virginia preferred
  • Current BCLS or ACLS certification required
  • OCN, SoCRA, or ACRP certification preferred

WORK 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. While performing the duties of this job, the employee is regularly exposed to direct contact with patients with potential for exposure to toxic substances, medicinal preparations, and chemotherapeutic agents.

PHYSICAL DEMANDS:
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 full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. 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.

Qualifications:
  • Experience in clinical research preferred
  • Experience with computer data entry and database management
  • Excellent written and oral communication skills
  • Ability to read, analyze, and interpret technical procedures such as protocols, informed consent, and regulatory documents
  • Graduate from an accredited program for nursing education (BSN preferred)
  • Minimum of one (1) year nursing experience, preferably in oncology
  • Current licensure as an RN in Virginia preferred
  • Current BCLS or ACLS certification required
  • OCN, SoCRA, or ACRP certification preferred

WORK 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. While performing the duties of this job, the employee is regularly exposed to direct contact with patients with potential for exposure to toxic substances, medicinal preparations, and chemotherapeutic agents.

PHYSICAL DEMANDS:
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 full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. 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.

Education:UNAVAILABLEEmployment Type: FULL_TIME

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