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Weekend Irb Jobs in Reston, VA (NOW HIRING)

NJ Retina

Clinical Research Coordin

Fairfax, VA

$49K - $70K/yr

Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions * Documents adverse events and notifies PI, sponsor and IRB * Assumes test article ...

Virginia Heart

Clinical Research Coordinator

Leesburg, VA

$24.50 - $32.50/hr

No Nights, weekends, or holidays! * Affordable Medical, Dental and Vision plans * 401(k) Retirement ... Coordinate study start-up activities, including IRB submission, site initiation visits, and pre ...

PRISM Vision Group

Clinical Research Coordin

Fairfax, VA · On-site

$49K - $70K/yr

Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions * Documents adverse events and notifies PI, sponsor and IRB * Assumes test article ...

Constellis

Quality/Cost Contain Reviewer

Herndon, VA · On-site

Support preparation and data gathering for Investigator Review Board (IRB) activities. * Provide ... Business work hours are Monday-Friday standard core hours, however some extended or weekend hours ...

Constellis

Quality/Cost Contain Reviewer

Herndon, VA · On-site

Support preparation and data gathering for Investigator Review Board (IRB) activities. * Provide ... Business work hours are Monday-Friday standard core hours, however some extended or weekend hours ...

IQVIA

Research Coordinator

Arlington, VA

Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient * Collaborates with the physician ...

IQVIA

Research Coordinator

Fairfax, VA

Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient * Collaborates with the physician ...

IQVIA

Research Coordinator

Fairfax, VA

Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient * Collaborates with the physician ...

IQVIA

Research Coordinator

Arlington, VA

Ensures that the most current version of the IRB approved protocol consent document is used by the physician investigator when consenting or re-consenting a patient * Collaborates with the physician ...

Qiagen

Clinical Research Associate

Germantown, MD · On-site

$65K - $75K/yr

Coordinating startup processes including IEC/IRB (Ethics Committee) and regulatory submissions, contracts and site activation activities. * Organizing instrument set-up, operational qualification and ...

Medix

Clinical Research Coordinator

Falls Church, VA · On-site

$30.77 - $37.98/hr

In-depth working knowledge of GCP, GDA, and IRB requirements. * Hands-on experience with clinical trial management systems (CTMS), EDC platforms, and Microsoft Office. * Bachelor's degree in a ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

May assist with submission of applications notifications to Institutional Review Board IRB Ethics Committee EC Regulatory Authority. * May assist with site recruitment oversight activities such as ...

Emmes

Senior Clinical Research Associate

Rockville, MD · On-site +1

May assist with submission of applications/notifications to Institutional Review Board (IRB)/Ethics Committee (EC)/Regulatory Authority. * May assist with site recruitment oversight activities such ...

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Showing results 1-20

All JobsWeekend Irb JobsWeekend Irb Jobs in Reston, VA

Weekend Irb information

What is the difference between Weekend IRB vs IRB Coordinator?

AspectWeekend IRBIRB Coordinator
CertificationsOften requires IRB-related training, but not always formal certificationsTypically requires IRB or research compliance certifications
Work EnvironmentPart-time, flexible hours, often on weekends or eveningsFull-time, office-based, regular weekday schedule
Employer & IndustryResearch institutions, hospitals, universitiesResearch institutions, hospitals, universities

Weekend IRB roles focus on providing oversight during non-standard hours, often with flexible schedules, while IRB Coordinators handle ongoing compliance, documentation, and communication during regular hours. Both roles are essential in research oversight but differ mainly in work hours and specific responsibilities.

What are Weekend IRB jobs?

Weekend IRB jobs refer to positions related to Institutional Review Boards (IRBs) that operate or require work during weekends. IRBs are committees established to review and approve research involving human subjects, ensuring ethical standards are met. Weekend IRB staff may include coordinators, administrators, or reviewers who process submissions, review protocols, and ensure compliance outside of normal weekday hours to accommodate researchers' needs and deadlines.

What are the typical responsibilities of a Weekend IRB member, and how do they contribute to the review process?

As a Weekend IRB (Institutional Review Board) member, your primary responsibility is to review research protocols submitted for ethical and regulatory compliance, particularly those requiring urgent or expedited consideration over weekends. This role often involves collaborating remotely with fellow board members, principal investigators, and compliance staff to ensure timely feedback on submissions. Challenges may include balancing multiple protocols with tight deadlines and maintaining clear communication despite limited in-person interaction. Your input directly impacts participant safety and institutional compliance, making attention to detail and ethical judgment essential.

What are the key skills and qualifications needed to thrive as an IRB (Institutional Review Board) member, and why are they important?

To thrive as an IRB member, you generally need a background in research ethics, regulatory compliance, and relevant academic or clinical experience, often supported by advanced degrees in health, law, or social sciences. Familiarity with federal regulations (such as 45 CFR 46), online protocol management systems, and human subjects protection certifications (e.g., CITI Program) is typically required. Strong analytical thinking, attention to detail, impartiality, and effective communication skills distinguish outstanding IRB members. These skills ensure that research protocols are ethically reviewed, participant rights are protected, and institutional compliance is maintained.
What are the most commonly searched types of Irb jobs in Reston, VA? The most popular types of Irb jobs in Reston, VA are:
What cities near Reston, VA are hiring for Weekend Irb jobs? Cities near Reston, VA with the most Weekend Irb job openings:
Weekend Irb jobs near you
Clinical Research Program Specialist (Oncology)

Clinical Research Program Specialist (Oncology)

Johns Hopkins University

Washington, DC • On-site

$48K - $84K/yr

Full-time

Posted 28 days ago

Johns Hopkins Medicine rating

7.5

Company rating: 7.5 out of 10

Based on 202 frontline employees who took The Breakroom Quiz

229th of 876 rated healthcare providers

Job description

Under limited supervision of the Sr. Clinical Research Program Manager, we are seeking a Clinical Research Regulatory Specialist who will be responsible for managing regulatory maintenance of clinical trials, assisting development of investigator-initiated studies, maintaining sponsor relationships, and facilitating compliance and continuing education trainings for the specific Oncology Clinical Research Program. Regulatory maintenance activities include amendment applications to the IRB and other regulatory agencies, and internal quality control of regulatory document management. This position requires a high level of knowledge, oversight, and organization, and will serve as a central resource for faculty conducting clinical research. Responsibilities will also include orient and train research staff in the program, assist budget development and oversee overall study coordination, and support general operations of the program.
Specific Duties & Responsibilities
  • Work closely with Program Manager and PI's to evaluate study status and complete regulatory requirements, including protocol submissions to IRB and relevant ancillary groups for smooth and timely implementation of protocol amendments.
  • Assist with revision of investigator-initiated studies; assure protocols, amendments, consent forms, and study operation manuals have complete, consistent language throughout, including proper SAE reporting requirements, coordinating center requirements, etc.
  • Work closely with PI's and sponsors to complete all study amendment submissions to the IRB, Cancer Center Cores (such as Sibley TSCRC Lab and IDS Pharmacy), and other required regulatory documents.
  • Track each protocol through Oncology and IRB approval process, evaluate for recurrent problems, develop and implement systems to decrease delay in the approval process.
  • For National Cancer Institute trials where Sibley is the lead site, work closely with the project manager and PI to submit the signature institution worksheet for approval, schedule study start-up meeting, maintain communication to ensure high quality of data, timely submission of data, and adherence to guidelines.
  • Conduct internal quality assurance measures, including periodic monitoring and training sessions, to ensure all clinical research faculty and staff within the program are up-to-date with regulatory guidelines, standard operating procedures, and certification requirements.
  • Maintain a continued high level of expertise in institutional databases including Epic, OnCore, eReg, eIRB, using this proficiency to ensure accurate data and analysis are sustained for all trials within the program.
  • Assist Program Manager with program operations and staff orientation and training - providing suggestions for improved procedures, creating checklists and program-related standard operating procedures.
  • Participate as requested in Cancer Center initiatives such quality-improvement workgroups and committee meetings.
  • Complete minimum requirements for continuing education units. Maintain up-to-date knowledge of and comply with Good Clinical Practice, ICH Guidelines, and SKCCC Clinical Research Office policies.
  • Ensure that Cancer Center policies, standard operating procedures, and guidelines related to the conduct of clinical trials are followed.

Minimum Qualifications
  • Bachelor's Degree in a related field.
  • Five years of related experience in clinical research in an academic.
  • Minimum of 2 years' experience in clinical trial and/or clinical research in a patient setting required.
  • Additional education may substitute for required experience, and additional related experience may substitute for required education beyond a high school diploma/graduation equivalent, to the extent permitted by the JHU equivalency formula.

Preferred Qualifications
  • Certification as a Clinical Research Professional is preferred.

Classified Title: Clinical Research Regulatory Specialist
Job Posting Title (Working Title): Clinical Research Program Specialist (Oncology)
Role/Level/Range: ACRP/04/MC
Starting Salary Range: $48,000 - $84,100 Annually ($65,400 targeted; Commensurate w/exp.)
Employee group: Full Time
Schedule: Mon - Fri / 8a -4:30p
FLSA Status: Exempt
Location: Hybrid/District of Columbia
Department name: SOM Onc Sibley
Personnel area: School of Medicine

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