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Full Time Irb information

See Spring, TX salary details

$55.2K

$293.7K

$356K

How much do full time irb jobs pay per year?

As of Jul 16, 2026, the average yearly pay for full time irb in Spring, TX is $293,723.00, according to ZipRecruiter salary data. Most workers in this role earn between $276,800.00 and $343,100.00 per year, depending on experience, location, and employer.

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.

What are the typical responsibilities of a full-time IRB (Institutional Review Board) 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 (Institutional Review Board) 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 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 popular job titles related to Full Time Irb jobs in Spring, TX? For Full Time Irb jobs in Spring, TX, the most frequently searched job titles are:
What cities near Spring, TX are hiring for Full Time Irb jobs? Cities near Spring, TX with the most Full Time Irb job openings:
Full Time Irb jobs near you
Research Coordinator I - Medicine - Gastroenterology and Hepatology

Research Coordinator I - Medicine - Gastroenterology and Hepatology

Baylor College of Medicine

Houston, TX • On-site

Full-time

Posted 5 days ago

Baylor College of Medicine rating

8.6

Company rating: 8.6 out of 10

Based on 21 frontline employees who took The Breakroom Quiz

56th of 555 rated colleges and universities

Job description

Summary

The Department of Medicine, Section of Gastroenterology and Hepatology at Baylor College of Medicine is seeking a Research Coordinator I to oversee the day-to-day activities of IBD (Inflammatory Bowel Disease) clinical trials. This is a full-time, on-site position offering the opportunity to work closely with a collaborative team and principal investigators.

The ideal candidate will manage IRB submissions, regulatory compliance, and budget components for multiple grants. Additional responsibilities include overseeing data collection, supporting patient recruitment and enrollment through opt-out mailed invitations, and conducting standardized telephone surveys.

Job Duties
  • Interview, administer surveys, screen, and recruit patients for multiple ongoing therapeutic and non-therapeutic clinical trials; explain study processes and procedures to educate participants.
  • Schedule research participants for tests and procedures, including laboratory tests, X-rays, and other protocol-specific studies.
  • Communicate with patients throughout the duration of the study, as needed.
  • Complete on-the-job training in blood draws, EKGs/ECGs, and vital signs collection prior to performing procedures on study participants.
  • Collect, process, ship, and maintain documentation for blood and/or biological specimens in accordance with study protocol requirements.
  • Assist with daily administrative tasks, including preparing study materials, photocopying, organizing and filing documents, mailing materials, and maintaining confidential files.
  • Provide detailed patient information related to study participation, including scheduling and coordinating follow-up visits.
  • Assist with maintenance of Institutional Review Board (IRB) documents for active studies, including submission of amendments and continuing reviews.
  • Order and organize laboratory research supplies and equipment.
  • Enter clinical trial data into sponsor electronic data capture (EDC) systems and ensure data accuracy and completeness.
  • Perform other duties as assigned.
Minimum Qualifications
  • High School diploma or GED.
  • Three years of relevant experience.
Preferred Qualifications
  • Bachelor's degree in a related field. No experience required with preferred degree.
  • Organized, self-motivated, teamwork, works well under pressure, multitasking.

Work Authorization Requirement:

This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment. 

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

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