ZipRecruiter

Log In

1

Research Integrity Jobs in Virginia (NOW HIRING)

Web Business Solutions Inc.

Research Assistant

Quantico, VA · On-site

$20.75 - $28.50/hr

Manage data entry and ensure the accuracy and integrity of data collected throughout the research process. * Prepare summaries and reports based on research findings, presenting data in clear and ...

Posted today

Web Business Solutions Inc.

Research Assistant

Quantico, VA · On-site

$20.75 - $28.50/hr

Manage data entry and ensure the accuracy and integrity of data collected throughout the research process. * Prepare summaries and reports based on research findings, presenting data in clear and ...

Posted today

HCA HealthONE Rose

Research Nurse

Richmond, VA · On-site

Research Nurse Experience the HCA Healthcare difference where colleagues are trusted, valued ... Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by ...

New

Chippenham Hospital

Research Nurse

Richmond, VA · On-site

Research Nurse Experience the HCA Healthcare difference where colleagues are trusted, valued ... Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by ...

TriStar StoneCrest

Research Nurse

Richmond, VA · On-site

Research Nurse Experience the HCA Healthcare difference where colleagues are trusted, valued ... Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by ...

New

previous pagenext page

Showing results 21-40

All JobsResearch Integrity JobsResearch Integrity Jobs in Virginia

Research Integrity information

See Virginia salary details

$10

$37

$82

How much do research integrity jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for research integrity in Virginia is $37.31, according to ZipRecruiter salary data. Most workers in this role earn between $20.57 and $48.39 per hour, depending on experience, location, and employer.

What is research integrity?

A Research Integrity job focuses on promoting ethical research practices, ensuring compliance with institutional and regulatory policies, and handling issues such as research misconduct, plagiarism, and data integrity. Professionals in this role may develop training programs, conduct investigations, and advise researchers on best practices. Their work helps maintain public trust in research and uphold academic and scientific standards.

What are the main responsibilities of someone working in research integrity?

Professionals in Research Integrity are responsible for reviewing research proposals and protocols to ensure compliance with ethical standards and institutional policies, investigating potential cases of research misconduct, and providing guidance and training to researchers on responsible practices. They regularly collaborate with faculty, administrative staff, and regulatory bodies to uphold and promote integrity across all stages of research. Typical days may involve auditing project documentation, drafting reports, and participating in committees or training sessions. This role plays a crucial part in protecting both the reputation of the institution and the validity of scientific findings.

What are the key skills and qualifications needed to thrive in research integrity, and why are they important?

To thrive in a Research Integrity role, you need an in-depth understanding of research ethics, regulatory compliance, and scientific methodologies, typically supported by advanced degrees in science or related fields. Familiarity with tools such as plagiarism detection software, research management systems, and guidelines from agencies like the Office of Research Integrity is often required. Exceptional attention to detail, strong analytical thinking, and effective communication are key soft skills in this position. These competencies are vital to ensure ethical conduct in research, maintain institutional credibility, and support responsible scientific advancement.

What are the most commonly searched types of Research Integrity jobs in Virginia?

The most popular types of Research Integrity jobs in Virginia are:

What are popular job titles related to Research Integrity jobs in Virginia?

For Research Integrity jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Research Integrity jobs in Virginia look for?

The top searched job categories for Research Integrity jobs in Virginia are:

Research Integrity jobs near you
Infographic showing various Research Integrity job openings in Virginia as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $77,614 per year, or $37.3 per hour.

Clinical Research Coordinator

Alcanza Clinical Research

Charlottesville, VA • On-site

$24 - $32/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 25 days ago

Job description

Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in  MA, NH, MI, VA, SC, FL, GA and AL. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.  

Key Responsibilities
In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 
  • Screening of patients for study enrollment;
  • Patient consents;
  • Patient follow-up visits;
  • Documenting in source clinic charts;
  • Entering data in EDC and answers queries;
  • Obtaining vital signs and ECGs;
  • May perform basic lab procedures per protocol, such as:  blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; 
  • Requesting and tracking medical record requests;
  • Updating and maintaining logs, chart filings; 
  • Maintaining & ordering study specific supplies;
  • Scheduling subjects for study visits and conducts appointment reminders;
  • Building/updating source as needed;
  • Conducting monitoring visits and resolves issues as needed in a timely manner;
  • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
o    Filing SAE/Deviation reports to Sponsor and IRB as needed;
o    Documenting and reporting adverse events;
o    Reporting non-compliance to appropriate staff in timely manner;
o    Maintaining positive and effective communication with clients and team            
       members;
o    Always practicing ALCOAC principles with all documentation;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
  • Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
  • Assist with training of new research assistants and coordinators;
  • Assist with scheduling and planning for visit capacity for assigned studies;
  • May set up, train and maintain all technology needed for studies;
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • May handle more complex study assignments and volumes;
  • May participate in community outreach / education events;
  • Maintaining confidentiality of patients, customers and company information,       and;
  • Performing all other duties as requested or assigned.


Skills, Knowledge and Expertise
Minimum Qualifications:  A Medical Assistant diploma, LPN/LVN, EMT credential AND 1+ years of clinical research coordination experience, OR an equivalent combination of education and experience, is required.  Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred.  CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.  

 Required Skills: 
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills. 
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines. 

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire. 
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.