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Full Time Clinical Research Rater Jobs in Virginia

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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 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

Senior Clinical Research Coordinator

Virginia Heart

Falls Church, VA

$37/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

Job description

Location: Fairfax, VA Status:  Full-Time/Non-Exempt Salary Range:  $37.00+  

Are you looking for new career opportunities, great wages, excellent benefits, and work-life balance?   Follow your heart to Virginia Heart!

At Virginia Heart, we are looking for a professional Senior Clinical Research Coordinator will plan, direct, evaluate and analyze clinical research trials related to cardiac drug and device trials.  Maintaining GCP/ICH guidelines and FDA regulations is always required.    

When you work with Virginia Heart, you will enjoy a dedicated and experienced staff, competitive wages, excellent benefits and the following rewards and incentives:

  • No Nights, weekends, or holidays!
  • Affordable Medical, Dental and Vision plans
  • 401(k) Retirement Plan
  • Paid Short-Term Disability
  • Employee Assistance Program for Mental and Physical well-being
  • Three Weeks of Paid Vacation upon eligibility
  • One week of Paid Sick Leave
  • Annual Merit-Based increases
  • Career Advancement Opportunities
  • Employee Referral Bonuses
  • Employee Discount Programs
  • Quarterly Employee Appreciation Events to include therapy dogs, raffles, and other fun events.

Virginia Heart is Northern Virginia's premier cardiovascular practice, bringing an unparalleled standard of excellence to our patients. We are seeking experienced professionals to join our team in our outpatient cardiology setting.  Every employee, at every level, begins their journey at Virginia Heart learning about the history of the organization and its established culture built on trust and integrity. Our employees drive this culture, and we want you to be a part of it. 

Roles and Responsibilities:  

  • Oversee Complex studies to ensure compliance with protocols and with relevant federal, state regulations, and institutional policies. Ensure that all regulatory files are complete, accurate, and up to date.
  • Coordinate study start-up activities, including IRB submission, site initiation visits, and pre-study visits. 
  • Provide leadership and guidance to junior research staff.
  • Serve as the primary point of contact for sponsors. 
  • Maintain detailed study records, including case report forms, drug dispensation records, and regulatory documents. 
  • Monitor patient enrollment, track retention and dropout information, and document follow-up and outreach efforts.   
  • Assess potential patients' eligibility by reviewing medical records, conducting interviews, and collaborating with providers.
  • Responsible for education and appropriate documentation of patient-informed consent. 
  • Record and report adverse events and side effects in consultation with investigators, ensuring timely submission to oversight agencies.
  • Prepare for and participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identify protocol deviations and assist in problem resolution efforts, such as protocol revisions. 
  • Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.  
  • Participate in preparation and management of research budgets and monetary disbursements. 
  • Conduct monitoring visits and resolve issues as needed in a timely manner. 
  • Mentor and train junior research staff and new team members on study protocol, procedures, and regulatory compliance.  
  • 10% Travel Required 

Skill Requirements and Qualifications:

  • Minimum of 4 years of clinical research experience.
  • Registered Nurse Licensure, or bachelor's degree in healthcare or related field strongly preferred
  • Must hold one of the following credentials: Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP)
  • Strong organizational and analytical skills required.
  • In-depth knowledge of Good Clinical Practice (GCP), FDA regulations, and IRB requirements.
  • Proficiency and clinical trial management systems and electronic data capture platforms.
  • Flexibility with working hours to accomadate study needs.
  • Detail-oriented, excellent written and verbal communication skills.
  • Excellenttime management skills and ability to work independently.
  • EMR experience, (EPIC a plus) and Microsoft Excel, Word and Outlook 

 (Click link to view other available openings and locations for our company: https://virginiaheart.hiringplatform.com/list/careers)