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Full Time Irb Jobs in Virginia (NOW HIRING)

ObjectiveHealth

Clinical Research Coordinator II

Richmond, VA · On-site

$22.25 - $29.75/hr

... the full-time position of Clinical Research Coordinator II. The ideal candidate will possess 3+ ... Skilled in all aspects required for conducting an IRB approved clinical trial protocol ...

Alcanza

Clinical Research Coordinator

Fredericksburg, VA · On-site

$23.75 - $31.75/hr

Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team ... guidelines. * Full-time employees regularly scheduled to work at least 30 hours per week are ...

Alcanza Clinical Research

$23.50 - $31.25/hr

Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team ... Benefits * Full-time employees regularly scheduled to work at least 30 hours per week are benefits ...

Inova

Research Project Associate

Fairfax, VA · On-site

$25.61 - $41.74/hr

This full-time role will be day-shift working Monday - Friday located in Fairfax, VA. The Research ... Assists in notifying the IRC, Research Manager/department director, PI, IRB, sponsor and other ...

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All JobsIrb JobsFull Time Irb JobsFull Time Irb Jobs in Virginia

Full Time Irb information

What is a full time IRB?

A Full Time IRB (Institutional Review Board) professional is a specialist who works full-time to review, approve, and oversee research involving human subjects to ensure that ethical standards and regulatory requirements are met. They are responsible for protecting the rights and welfare of research participants by conducting ethical reviews, monitoring ongoing research, and providing guidance to researchers. Full Time IRB staff often work in universities, hospitals, or research institutions, and collaborate closely with researchers and compliance officers. Their role is essential to maintaining the integrity and safety of scientific research involving humans.

What are the typical responsibilities of a full time IRB coordinator, and how does the role interact with researchers and regulatory bodies?

A full-time IRB coordinator is responsible for managing the ethical review process of research involving human subjects. This includes reviewing research proposals for compliance with federal regulations, facilitating IRB meetings, communicating required changes to researchers, and maintaining accurate records. Coordinators act as a critical liaison between researchers, IRB members, and regulatory agencies to ensure studies are conducted ethically and participants are protected. Daily tasks often involve document review, correspondence, and providing guidance to investigators, making strong communication and organizational skills essential.

What are the key skills and qualifications needed to thrive as a full time IRB professional, and why are they important?

To thrive as a full-time IRB professional, you need a comprehensive understanding of research ethics, regulatory compliance (such as 45 CFR 46 and FDA regulations), and typically a background in life sciences or healthcare. Familiarity with electronic IRB management systems, compliance databases, and certifications like CIP (Certified IRB Professional) are commonly required. Strong analytical thinking, attention to detail, and effective communication are essential soft skills for reviewing protocols and collaborating with researchers. These competencies are critical for ensuring the protection of human research subjects and maintaining institutional and federal compliance.

What is the difference between Full Time Irb vs Part Time Irb?

AspectFull Time IrbPart Time Irb
CredentialsIRB certification, research ethics trainingIRB certification, research ethics training
Work EnvironmentOffice, research institutions, hospitalsFlexible, part-time settings, remote options
Employer & IndustryResearch institutions, hospitals, universitiesResearch organizations, academic institutions
Work Hours40+ hours/weekLess than 20 hours/week

Full Time Irb roles typically involve a standard 40+ hour workweek, requiring full-time commitment and consistent presence in research settings. Part Time Irb positions offer flexible hours, often less than 20 hours weekly, suitable for those balancing other responsibilities. Both roles require IRB certification and knowledge of research ethics, but the main difference lies in hours and work setting.

How to become a full time IRB?

To become a full-time IRB (Institutional Review Board) member, individuals typically need a background in research, ethics, or related fields, along with experience in human subjects research. Certification in research ethics or compliance, such as CITI Program training, is often required, and strong analytical and communication skills are essential for reviewing research protocols. Full-time IRB roles may also require familiarity with federal regulations like the Common Rule and institutional policies.

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

The most popular types of Irb jobs in Virginia are:

What are popular job titles related to Full Time Irb jobs in Virginia?

For Full Time Irb jobs in Virginia, the most frequently searched job titles are:

What job categories do people searching Full Time Irb jobs in Virginia look for?

The top searched job categories for Full Time Irb jobs in Virginia are:

Full Time Irb jobs near you
Infographic showing various Full Time Irb job openings in Virginia as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Clinical Research Assistant

Prism Vision Group

Fairfax, VA

$46K - $96K/yr

Full-time

Posted 10 days ago

PRISM Vision Group rating

7.2

Company rating: 7.2 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

Job description

This exempt, onsite role is located at Retina Group of Washington, Fairfax, VA location, which is part of Prism Vision Group.

Compensation Range: $46,675.20 - $96,969.60/annual (Dependent on Experience)

The Clinical Research Assistant reports to the RGW Office Manager and RGW Research Lead and will aid in the coordination and conduct of research under the supervision of a designated physician. The Clinical Research Assistant will perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Clinical Research Assistant will develop knowledge of the research studies, rationale, subjects and procedures associated with the studies as designated by the Senior/Lead Clinical Research Coordinator. This  position is designed specifically to develop into a Clinical Research Coordinator and travels between multiple locations as needed.

Role and Responsibilities:

  • Assists in recruitment efforts to screen potential patients for eligibility for studies.
  • Obtains informed consent from patients and conducts study visits for clinical trials
  • Creates Case Report Forms
  • Completes assessments on study subjects as per protocol
  • Documents study assessments
  • Enters study data into EDC systems
  • Collects, processes, stores and shipslab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessary
  • Coordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessary
  • Assists during Sponsor and FDA audits
  • Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions
  • Documents adverse events and notifies PI, sponsor and IRB under CRC guidance
  • Assumes test article accountability
  • Possesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility
  • Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certification
  • Travels to investigator meetings
  • Participates in weekly meetings with the research team, provides study metrics
  • Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner

Qualifications:

Education: Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.

Experience: 1+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)

Knowledge/Skills/Experience:

• Excellent Excel, Word, PowerPoint and reporting skills

• Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators

• Excellent organizational skills and self-management skills to independently manage workflow

• Ability to prioritize

• Meticulous attention to detail

• Knowledge of medical terminology

• Knowledge of good clinical practice, FDA, OHRP, HIPAA policies

• Experience using Microsoft Office Suite

• Certification through either ACRP or SoCRA highly preferred

Qualifications:

Qualifications:

Education: Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.

Experience: 1+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)

Knowledge/Skills/Experience:

• Excellent Excel, Word, PowerPoint and reporting skills

• Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators

• Excellent organizational skills and self-management skills to independently manage workflow

• Ability to prioritize

• Meticulous attention to detail

• Knowledge of medical terminology

• Knowledge of good clinical practice, FDA, OHRP, HIPAA policies

• Experience using Microsoft Office Suite

• Certification through either ACRP or SoCRA highly preferred

Education:UNAVAILABLEEmployment Type: FULL_TIME

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