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Temp Irb Analyst Jobs (NOW HIRING)

University of Miami

Research Associate 1

Miami, FL

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... IRB compliance to performing in-depth thematic data analysis and codebook development, the ...

The University of Miami

Research Associate 1

Miami, FL · On-site +1

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... IRB compliance to performing in-depth thematic data analysis and codebook development, the ...

Drexel University

Research Assistant

Philadelphia, PA · On-site

$19.50 - $26.75/hr

... and analysis, report and manuscript development, and deliverable development. The Headen Research ... University City - Philadelphia, PA Additional Information This is a Part-Time temporary position ...

University of Rochester

$21.36 - $29.90/hr

Temporary Time Type: Time as Reported / Per Diem Scheduled Weekly Hours: As Scheduled Department ... The HSRS also contributes to high-quality data collection and analysis, manuscript, grant, and ...

Drexel University

Research Assistant

Philadelphia, PA

$19.50 - $26.75/hr

... and analysis, report and manuscript development, and deliverable development. The Headen Research ... University City - Philadelphia, PA Additional Information This is a Part-Time temporary position ...

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All JobsTemp Irb Analyst Jobs

Temp Irb Analyst information

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$73.3K

$130K

How much do temp irb analyst jobs pay per year?

As of Jul 5, 2026, the average yearly pay for temp irb analyst in the United States is $73,261.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $87,000.00 per year, depending on experience, location, and employer.

What is the difference between Temp Irb Analyst vs Clinical Research Coordinator?

AspectTemp Irb AnalystClinical Research Coordinator
CredentialsBachelor's degree, IRB trainingBachelor's degree, clinical research training
Work EnvironmentOffice, regulatory agenciesClinical sites, hospitals
Industry UsageResearch institutions, pharmaHospitals, research sites
Primary FocusIRB review, complianceParticipant management, study coordination

The Temp Irb Analyst primarily focuses on IRB submissions and regulatory compliance, working closely with research protocols. In contrast, a Clinical Research Coordinator manages participant recruitment, scheduling, and day-to-day study activities. While both roles support clinical research, the Irb Analyst emphasizes regulatory review, whereas the Coordinator handles operational tasks at research sites.

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What cities are hiring for Temp Irb Analyst jobs? Cities with the most Temp Irb Analyst job openings:
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Temp Irb Analyst jobs near you
Infographic showing various Temp Irb Analyst job openings in the United States as of June 2026, with employment types broken down into 87% Full Time, 1% Part Time, 1% Temporary, and 11% Contract. Highlights an 81% Physical, 7% Hybrid, and 12% Remote job distribution, with an average salary of $73,261 per year, or $35.2 per hour.
Clinical Research Coordinator 1 Full Time Bascom Palmer Eye Institute Miami, FL

Clinical Research Coordinator 1 Full Time Bascom Palmer Eye Institute Miami, FL

The University of Miami

Miami, FL • On-site

$23.25 - $30.75/hr

Full-time

Medical, Dental

Posted 19 days ago

University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

224th of 544 rated colleges and universities

Job description

Current Employees:
If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.
The University of Miami, Bascom Palmer Eye Institute, has an exciting full time opportunity for a Clinical Research Coordinator in Miami, Florida.
The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines.
CORE JOB FUNCTIONS
  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols.
  • Maintains enrollment procedures according to the protocol.
  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.
  • Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.
  • Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.
  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
  • Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
  • Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Knows the contents and maintenance of study-specific clinical research regulatory binders.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE QUALIFICATIONS
Education:
Bachelor's degree in relevant field or equivalent
Experience:
Minimum 1 year of relevant experience
Knowledge, Skills and Attitudes:
• Skill in completing assignments accurately and with attention to detail.
• Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
• Ability to process and handle confidential information with discretion.
• Ability to work evenings, nights, and weekends as necessary.
• Commitment to the University's core values.
• Ability to work independently and/or in a collaborative environment.
Department Specific Functions
• Flexibility to travel to all BPEI sites as needed
• Establishes patient/participant screening procedures with Principal Investigator and obtains relevant medical information from patient clinic charts/medical records.
• Ability to handle multiple clinical trials with several principal investigators
• Serve as back up coordinator to other clinical trials
• Completes corrections/queries required at audits/monitor visits and takes action to correct deviations as needed.
• Establishes/maintains contact with patient/participants, health care providers, community agencies and study sponsors.
• Updates appropriate agencies (such as sponsors, IRB, etc) regarding current status of research project. Provides in-service education to staff and patients/participants about research protocols
• Prepares and submits annual reviews to the Institutional Review Board (IRB). Maintains consent forms and sponsor correspondences. Notifies IRB of protocol amendments, safety reports and serious adverse events, etc. in compliance with applicable regulations
• Implements research protocol and monitors participant adherence to protocol
The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.
UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.
Job Status:
Full time
Employee Type:
Staff

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About University of Miami

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The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Coral Gables, FL, US

Year founded

1925

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