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Weekend Irb Jobs in Reston, VA (NOW HIRING)

Cape Fox SS

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Supports assembly, development and review of new research projects. - Work with staff on manuscript preparation for research studies and manuscript submission. - Prepare materials for IRB submission ...

Icon plc

Senior Clinical Research Associate

Washington, DC · Hybrid

$110K - $138K/yr

Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals * Regularly review site Key Risk Indicator (KRI)metrics,issuesandaction items to ...

ICON

Senior Clinical Research Associate

Washington, DC · On-site +1

$110K - $138K/yr

Support sites with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and confirm approvals * Regularly review site Key Risk Indicator (KRI) metrics, issues and action items to ...

Axle

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Monitor and coordinate activities associated with protocol development, protocol amendments, IRB submissions, regulatory submissions, continuing reviews, study activation activities, and clinical ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Monitor and coordinate activities associated with protocol development, protocol amendments, IRB submissions, regulatory submissions, continuing reviews, study activation activities, and clinical ...

Axle

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Monitor and coordinate activities associated with protocol development, protocol amendments, IRB submissions, regulatory submissions, continuing reviews, study activation activities, and clinical ...

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All JobsIrb 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 is a weekend IRB?

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?

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 a weekend IRB member?

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 Coordinator

Cape Fox SS

Bethesda, MD

$26 - $34.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description

Concentric Methods is seeking an experienced Clinical Research Coordinator to independently provide support services to the NIH. The total hourly pay for this non-exempt position is $30.00 for up to 40 hours per week. This rate represents the company's good faith and reasonable estimate of possible compensation at the time of posting

In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn. Supports clinical staff develop, implement and maintain clinical research data files and materials.

- Assist preparing and submitting for review accurate source documents related to all research procedures. Collects research data and prepares information for inputs and analysis. - Work with staff on data acquisition and analysis using a variety of methods, including recruitment, entry, management and display for the Department of Bioethics research studies.

Supports the development of forms and questionnaires. - Work with staff to coordinate the logistics of courses and workshops, including the course Ethical and Regulatory Aspects of Clinical Research, and the Empirical Research Lab. Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.

- Conduct literature searches; gather and synthesize background information. Monitors subject's progress and reports adverse events. - Assist staff writing progress reports and contributions to peer-reviewed scientific manuscripts.

Supports assembly, development and review of new research projects. - Work with staff on manuscript preparation for research studies and manuscript submission. - Prepare materials for IRB submission, manuscript transmittals and other necessary approvals and reviews.

Supports the creation and management of clinical websites and web-based tools. - Collaborate with staff on the maintenance of Departmental metrics, databases and website.Preferred Professional Experience: Manuscript preparation - Data acquisition - Coordinating events - Protocol development - Statistical Analysis - Recruitment - Research Familiarity with STATA and NVivo Education and Certifications: Bachelor's Degree Required Two years of related experience Core Skills: Strong organizational and time management skills. Excellent interpersonal and communication skills

Attention to detail in data collection and documentation. Proficiency in relevant computer applications and software. Ability to work both independently and collaboratively.

Problem-solving and critical-thinking abilities.Preferred Professional Experience: Manuscript preparation - Data acquisition - Coordinating events - Protocol development - Statistical Analysis - Recruitment - Research Familiarity with STATA and NVivo Education and Certifications: Bachelor's Degree Required Two years of related experience Core Skills: Strong organizational and time management skills. Excellent interpersonal and communication skills. Attention to detail in data collection and documentation

Proficiency in relevant computer applications and software. Ability to work both independently and collaboratively. Problem-solving and critical-thinking abilities.

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