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Full Time Irb Jobs in Spring, TX (NOW HIRING)

Alcanza

Clinical Research Coordinator

Katy, TX · On-site

$22.25 - $29.50/hr

Filing SAE/Deviation reports to Sponsor and IRB as needed; * Documenting and reporting adverse ... guidelines. * Full-time employees regularly scheduled to work at least 30 hours per week are ...

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All JobsIrb JobsFull Time Irb JobsFull Time Irb Jobs in Spring, TX

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 Sep 11, 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 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 job categories do people searching Full Time Irb jobs in Spring, TX look for?

The top searched job categories for Full Time Irb jobs in Spring, TX 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
Infographic showing various Full Time Irb job openings in Spring, TX as of September 2026, with employment types broken down into 1% As Needed, 85% Full Time, and 14% Part Time. Highlights an 81% Physical, 3% Hybrid, and 16% Remote job distribution, with an average salary of $293,723 per year, or $141.2 per hour.

Senior Research Coordinator - Neurosurgery

Houston, TX • On-site

Baylor College of Medicine
Colleges, Universities, and Professional Schools • 5 - 10K employees
Learn more about Baylor College of Medicineexternal

$70K - $83K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Baylor College of Medicine rating

8.0

Company rating: 8.0 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

Job description

Senior Research Coordinator - Neurosurgery
Division: Neurosurgery
Work Arrangement: Onsite only
Location: Houston, TX
Salary Range: $70,618 - $83,080
FLSA Status: Exempt
Work Schedule: Monday - Friday, 8 a.m. - 5 p.m.
Summary
We are seeking a qualified, experienced, professional who possesses advanced knowledge of clinical research practices for a full-time position. This position will function in the clinical research section of the Department of Neurosurgery and Cain Foundation Laboratories. The personnel will function in a capacity in which they manage, coordinate, and facilitate first-in-human trial program to test various therapies for pediatric epilepsy and related disorders. The personnel will provide administrative, regulatory, and operational support for clinical and translational research studies. Responsibilities include managing scheduling and personnel activities, coordinating IRB and FDA submissions, assisting in clinical trial agreement processes, and Interfacing with hospital finance for trial costs. The ideal candidate is highly organized, detail-oriented, and experienced in navigating regulatory requirements and cross-functional collaboration within an academic medical center or clinical research environment.
Job Duties
40% Administrative Support
  • Coordinate daily administrative activities for the research team, including managing calendars, scheduling meetings, and tracking project deadlines.
  • Process purchases for research supplies and services, as well as travel requests and reimbursement paperwork.
  • Assist with personnel-related activities, including onboarding, hiring documentation, and maintaining employee records.
  • Prepare letters, reports, meeting materials, and other routine documents. Maintain organized research files and records.
  • Serve as a point of contact for investigators, staff, and collaborators by responding to questions and coordinating communications.

40% Regulatory Support
  • Prepare and submit IRB applications, amendments, continuing reviews, and study closures for human research studies.
  • Coordinate required approvals with institutional and hospital offices before studies begin and throughout the life of the project.
  • Assist with FDA submissions, including Investigational Device Exemption (IDE) applications, amendments, and annual renewals, when applicable.
  • Maintain regulatory files and ensure study documentation is complete and up to date.

20% Contract and Financial Coordination
  • Coordinate the clinical trial agreement (CTA) process by working with investigators, sponsors, and institutional contracting offices.
  • Work with hospital finance and research administration to support clinical trial budgets, research billing, and study-related financial processes.
  • Track contract and regulatory milestones to help ensure studies are activated on schedule.

Scope and Impact
  • Provides administrative, regulatory, and operational support.
  • Helps ensure research projects remain organized, compliant with institutional and federal requirements, and progress efficiently from study startup through completion.
  • Serve as point of contact for investigators, research staff, sponsors, and institutional partners regarding administrative and regulatory matters.
  • Develop and improve workflows, standard operating procedures (SOPs), and tracking tools to increase the efficiency of research operations.
  • Monitor study and regulatory deadlines to ensure timely completion of required submissions and approvals.
  • Assist with preparing documentation for internal reviews, sponsor monitoring visits, and regulatory audits.
  • Perform other duties and special projects as assigned to support departmental and institutional research objectives.

Minimum Qualifications
  • Bachelor's degree in a Basic Science or related field. Four years of related experience may substitute for degree requirement.
  • Five years of relevant experience.

Preferred Qualifications
  • Knowledge and experience of regulatory aspects of clinical research is a must.
  • Effective communication skills, both orally and in writing.
  • Ability to understand and implement research studies and protocols.
  • Interpersonal skills necessary to coordinate research studies.

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.
Requisition ID: 26036

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