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Full Time Irb Analyst Jobs in Colorado (NOW HIRING)

University of Colorado

Bilingual Research Specialist

Aurora, CO · On-site

$17.25 - $22.25/hr

... IRB submission and form implementation. This position can be offered at part-time (0.75 FTE) to full-time (1.0 FTE) depending on candidate preference and availability. This position reports to the ...

University of Colorado

Bilingual Research Specialist

Aurora, CO · On-site

$17.25 - $22.25/hr

... IRB submission and form implementation. This position can be offered at part-time (0.75 FTE) to full-time (1.0 FTE) depending on candidate preference and availability. This position reports to the ...

All JobsIrb Analyst JobsFull Time Irb Analyst JobsFull Time Irb Analyst Jobs in Colorado

Full Time Irb Analyst information

What is a full time IRB analyst?

Full Time IRB Analysts are professionals who review research proposals to ensure they comply with ethical standards and federal regulations for human subject research. They work within Institutional Review Boards (IRBs) at universities, hospitals, or research organizations. Their responsibilities include evaluating study protocols, ensuring informed consent, and safeguarding participants' rights and welfare. Full time analysts typically collaborate with researchers and provide guidance on regulatory requirements. This role requires strong attention to detail and knowledge of ethical research practices.

What are the key skills and qualifications needed to thrive as a full time IRB analyst?

To thrive as a Full Time IRB Analyst, you need a solid understanding of research ethics, regulatory compliance, and human subjects protection, often supported by a relevant degree in health sciences or a related field. Familiarity with electronic IRB management systems, federal regulations (like the Common Rule), and certifications such as CIP (Certified IRB Professional) are typically required. Strong analytical thinking, attention to detail, and effective communication skills help you interpret protocols and interact with researchers and committee members. These skills are crucial to ensure ethical research practices, regulatory compliance, and the protection of participants' rights and welfare.

What are some common challenges faced by full time IRB analysts, and how can they be managed effectively?

Full Time IRB Analysts often encounter challenges related to balancing regulatory compliance with facilitating research efficiency. Navigating complex federal regulations, staying updated on policy changes, and managing high volumes of protocol submissions can be demanding. Effective time management, strong communication skills for liaising with researchers and committee members, and continuous professional development are key to managing these challenges. Collaborative team environments and mentorship opportunities also help IRB Analysts stay informed and support each other.

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

AspectFull Time Irb AnalystPart Time Irb Analyst
Work HoursTypically 40 hours/weekLess than 20 hours/week
CertificationsOften requires IRB-related certificationsMay require similar certifications but on a part-time basis
Work EnvironmentFull-time, office or remotePart-time, flexible schedule
Employer UsageCommon in research institutions and biotech companiesLess common, often in consulting or freelance roles

Full Time Irb Analysts typically work 40 hours a week, with comprehensive responsibilities in overseeing research compliance. Part Time Irb Analysts work fewer hours, often with flexible schedules, focusing on specific tasks. Both roles require similar certifications and are used in research settings, but full-time positions offer more stability and broader responsibilities.

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

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

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

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

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

Clinical Research Coordinator

Vail Health Hospital

Edwards, CO • On-site

$26.75 - $35.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

Job description

This is a 3 year, grant funded role.
 
About the opportunity:
 
Responsible for verifying that the rights and well-being of human subjects are protected and that the reported trial data are accurate, complete and verifiable from source documents. Additionally, the Clinical Research Coordinator makes sure that the conduct of the trial is in compliance with currently-approved protocol/amendments(s) and with applicable regulatory requirements.
 
What you will do:
 
  • Responsible for the management of clinical trials, including: analysis of potential patient recruitment, preparation of trial-related documentation, ensuring the safety and proper conduct of the trial, organizing IRB/Ethics committee submissions, and continued communication between all parties involved.
  • Maintain files, including: IRB approvals, CV of investigators and study personnel, clinical investigator brochures, protocols, case report forms, consent documents, material shipping orders, letters of agreement, lab information, investigator and site correspondence, and schedules of payment.
  • Maintain records of initial sponsor correspondence, records of IRB submissions, amendments, budgets, contracts, and/ or approved consents. Monitor updates and closures online.
  • Manage patient recruitment strategies to increase patient accrual, including: investigator meetings, advertising, letters to appropriate physicians, being familiar with and distributing patient selection criteria, etc. Educate potential subjects on the details of the study.
  • Follow study management policies and procedures regarding the registration of all study candidates. Prepare patient packets, including: consent with updated IRB, eligibility checklist, protocol treatment calendar, and lab certificates & reference ranges. Coordinate the subjects treatment scheduling process, as required by protocol.
  • Complete Case Report forms for lab draws, proper storage of specimens, and preparation of shipping and receiving of specimens. Maintain, submit and track completed Case Report forms. Ensure that queries generated during cleaning are responded to in a timely manner.
  • Collaborate with clinical staff and Principle Investigator to ensure tests and procedures that are required by clinical protocols are performed and documented, and charges from pharmacy are billed correctly.
  • Initiate treatment and specimen collection. Maintain and document adequate follow-up with patients, physicians, and sponsors. Monitor and re-check nursing dosages to ensure the patient receives treatment per protocol and reports to SWOG organization.
  • Recognize and follows protocol for legal reporting of adverse events to appropriate parties (e.g. Principle Investigator, SWOG organization).
  • Attend investigator-coordinator meetings, initial orientations, study audits, and closeout visits.
This description is not intended and should not be construed to be an exhaustive list of all responsibilities, skills and efforts or work conditions associated with the job. It is intended to be an accurate reflection of the general nature and level of the job.
 
What you will need:
 
Experience:
  • Previous experience with clinical trials required.
  • Oncology-specific experience preferred.
Education:
  • N/A
License(s) and Certification(s):
  • Certified Clinical Research Professional certification preferred

Benefits at Vail Health (Full Time) Include:

  • Competitive Wages & Family Benefits:
    • Competitive wages
    • Parental leave (4 weeks paid)
    • Housing programs
    • Childcare reimbursement 
  • Comprehensive Health Benefits: 
    • Medical
    • Dental 
    • Vision
  • Educational Programs: 
    • Tuition Assistance 
    • Existing Student Loan Repayment
    • Specialty Certification Reimbursement
    • Annual Supplemental Educational Funds
  • Paid Time Off:
    • Up to five weeks in your first year of employment and continues to grow each year.
  • Retirement & Supplemental Insurance:
    • 403(b) Retirement plan with immediate matching 
    • Life insurance
    • Short and long-term disability
  • Recreation Benefits, Wellness & More:
    • Up to $1,000 annual wellbeing reimbursement
    • Recreation discounts
    • Pet insurance

Apply