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Internship Irb Analyst Jobs (NOW HIRING)

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Research Coordinator, Rheumatology

Dallas, TX

Prepare, submit, and maintain regulatory documentation with the Institutional Review Board (IRB ... Generate reports and organize data for statistical analysis. * Assist with the preparation and ...

Tranquil Clinical Research

Research Intern

Webster, TX · On-site

The Intern will primarily be responsible for the collection, aggregation, and analysis of data. The ... Accurately complete IRB submissions on time. * Anticipate study needs and work to accomplish them ...

Orlando Health

Dig Health Innov Coord Intern

Orlando, FL · On-site

$14 - $18.75/hr

  • Medical

  • Retirement

  • PTO

Internship- Temporary Hours: 20 hours/week-hours are flexible based on class schedule (must be ... Support market analysis activities including TAM/SAM assessments and stakeholder interview ...

DAN

Research Assistant-Diving Science

Durham, NC · On-site

It provides employment training, internships, and apprenticeship opportunities at over 3,000 public ... IRB protocols, data collection/storage, statistics). Then observe and participate in our ongoing ...

Oncodea

Molecular Diagnostics Associate

Saint Paul, MN · On-site

  • Medical

  • PTO

... IRB and HIPAA requirements. * Handle general lab operations: ordering, inventory, reagent ... internships and undergraduate research count). * Strong analytical skills and scientific curiosity.

DAN

Research Assistant-Diving Science

Durham, NC

It providesemployment training, internships, and apprenticeship opportunitiesat over 3,000 public ... IRB protocols, data collection/storage, statistics). Then observeand participate in our ongoing ...

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Internship Irb Analyst information

What is an Internship IRB Analyst?

An Internship IRB Analyst is a student or entry-level professional who assists with the review and oversight of research studies involving human subjects to ensure compliance with ethical standards and regulatory requirements. They work under the guidance of experienced IRB (Institutional Review Board) staff, helping to review research protocols, prepare documentation, and communicate with researchers. This role provides valuable experience in research ethics, regulatory affairs, and the protection of human subjects in research.

What are the key skills and qualifications needed to thrive as an Internship IRB Analyst?

To thrive as an Internship IRB Analyst, you need a solid understanding of research ethics, human subjects protection, and regulatory guidelines, typically gained through coursework in health sciences or related fields. Familiarity with IRB management software, federal compliance databases, and documentation systems is common for this role. Strong analytical thinking, attention to detail, and effective communication skills help interns review protocols and collaborate with researchers. These skills ensure ethical oversight, regulatory compliance, and the protection of research participants in institutional settings.

What are some common challenges faced by Internship IRB Analysts, and how can they be addressed?

Internship IRB Analysts often encounter challenges in interpreting complex research protocols and ensuring compliance with evolving ethical guidelines. Navigating the review process efficiently while balancing the need for thoroughness and timeliness can be demanding, especially when coordinating with researchers and senior IRB members. To address these challenges, it's helpful to develop strong communication skills, stay updated on institutional and federal regulations, and seek mentorship from experienced analysts. Regular training and proactive engagement with the IRB team also support skill development and confidence in decision-making.

What is the difference between Internship Irb Analyst vs Research Coordinator?

AspectInternship IRB AnalystResearch Coordinator
Required CredentialsTypically pursuing or recent graduate, some knowledge of IRB processesOften holds a degree in health sciences or related field, some certifications may be preferred
Work EnvironmentOffice setting, supporting IRB review processes, part-time or temporaryClinical or research site, managing study logistics and participant coordination
Employer & IndustryResearch institutions, universities, biotech companiesHospitals, research centers, academic institutions

The Internship IRB Analyst and Research Coordinator roles share some overlap in research settings and industry usage. However, the Internship IRB Analyst typically focuses on supporting IRB review processes and is often an entry-level or internship position, while the Research Coordinator manages broader study operations and participant interactions. Both roles are essential in research but differ in scope and responsibilities.

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Internship Irb Analyst jobs near you
Infographic showing various Internship Irb Analyst job openings in the United States as of August 2026, with employment types broken down into 89% Full Time, 5% Part Time, and 6% Contract. Highlights an 80% Physical, 9% Hybrid, and 11% Remote job distribution.

Research Coordinator

Scottish Rite for Children

Dallas, TX • On-site

Full-time

Re-posted yesterday

Scottish Rite For Children rating

8.5

Company rating: 8.5 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

55th of 1,060 rated hospitals

Job description

Our patients are our number one priority! We're committed to giving children back their childhood!
Job Posting Title:
Research Coordinator
Location:
Dallas - Hospital
Additional Posting Details:
Monday - Friday,
8:00am - 4:00pm
Job Description:
Duties/Responsibilities
  • Collaborate with staff in other research divisions and clinical departments within Scottish Rite to obtain the information and support necessary to conduct research. Organize and lead project meetings, communicate study updates, and provide regular reports to Principal Investigators.
  • Perform literature reviews, assist with study design, prepare regulatory documents, consent forms, and research submissions for presentations and publications.
  • Prepare, submit, and maintain regulatory documentation with the Institutional Review Board (IRB), Research Advisory Panel, and other applicable regulatory agencies, including initial submissions, continuing reviews, amendments, and study closures, while ensuring compliance with Good Clinical Practice (GCP), Human Subjects Protection, and applicable regulatory guidelines.
  • Develop and maintain project timelines, communicate barriers proactively, and coordinate with research teams to ensure milestones and deadlines are achieved.
  • Execute approved study protocols in accordance with GCP, institutional policies, and study requirements. Maintain regulatory binders, source documentation, and study files; manage reportable events, protocol deviations, adverse events, and audit readiness for internal, sponsor, and regulatory inspections.
  • Screen, recruit, consent, and enroll research participants while ensuring compliance with study protocols and regulatory requirements.
  • Coordinate study visits and procedures, including clinic visits, questionnaires, laboratory collections, imaging, and other protocol-required assessments. Monitor participant follow-up and protocol compliance.
  • Collect, enter, and maintain accurate research data using REDCap, electronic data capture systems, electronic medical records (Epic preferred), and study databases to ensure data quality and integrity. Resolve data queries and maintain study documentation.
  • Generate reports and organize data for statistical analysis.
  • Assist with the preparation and submission of abstracts, posters, presentations, manuscripts, and grant or funding applications.
  • Participate in internal, sponsor, and regulatory audits; identify process improvement opportunities and support corrective actions as appropriate.
  • Participate in onboarding, training, and coordinating research staff, interns, students, residents, and fellows.
  • Read literature relevant to pediatric medical and surgical conditions and attend conferences and educational meetings supporting ongoing research initiatives.
  • Support research activities across divisions, departments, or campuses as needed.
  • Perform other duties as assigned.

Required Skills/Abilities
  • Bachelor's degree required.
  • Prior clinical research and regulatory experience strongly preferred; three years of clinical research experience preferred.
  • Certification as a Certified Clinical Research Professional (CCRP) preferred.
  • Working knowledge of Good Clinical Practice (GCP), Human Subjects Protection, IRB processes, and clinical research regulatory requirements preferred.
  • Experience with REDCap or other electronic data capture systems preferred.
  • Experience with electronic medical records, particularly Epic, preferred.
  • Proficiency in Microsoft Office.
  • Strong organizational, time management, and project coordination skills with the ability to manage multiple studies simultaneously.
  • Excellent communication, problem-solving, critical thinking, and attention to detail.
  • Ability to work independently while collaborating effectively with multidisciplinary teams.
  • Self-motivated, adaptable, resourceful, and able to thrive in a fast-paced research environment.
  • Capable of recruiting research participants in person, by phone, and virtually.

Preferred Qualifications for Advanced/Senior Research Coordinators
  • Candidates with experience in IND/IDE studies, audit readiness, quality management, CAPA development, multi-site study coordination, SOP development, staff mentoring, project management, and sponsor interactions are encouraged to apply.

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