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Remote Ehs Analyst Jobs (NOW HIRING)

Otis

Manager, EH&S Southwest

Los Angeles, CA · Remote

$120K - $140K/yr

Nevada Home Office Remote Location, Remote City, NV, 06032 USA Manager, EHS, Southwest Each day ... We are seeking creative, analytic, results-focused safety professionals to contribute to our ...

REXEL

Manager Region Health & Safety

Dallas, TX · On-site +1

This position is remote when not traveling, but travel will be at least 50% of the time and we need ... Use some data analysis and statistics to inform decisions and demonstrate measurable EHS ...

Ocean Spray

Environmental Engineer

Sulphur Springs, TX · On-site +1

We are open to remote candidates. In this role, the Environmental Engineer is responsible for ... Ensure all required EHS permits are current, accurate, and maintained for operational compliance

New

Ocean Spray

Environmental Engineer

Seattle, WA · On-site +1

We are open to remote candidates. In this role, the Environmental Engineer is responsible for ... Ensure all required EHS permits are current, accurate, and maintained for operational compliance

New

Ocean Spray

Environmental Engineer

Dallas, TX · On-site +1

We are open to remote candidates. In this role, the Environmental Engineer is responsible for ... Ensure all required EHS permits are current, accurate, and maintained for operational compliance

New

Ocean Spray

Environmental Engineer

Bentonville, AR · On-site +1

We are open to remote candidates. In this role, the Environmental Engineer is responsible for ... Ensure all required EHS permits are current, accurate, and maintained for operational compliance

New

Ocean Spray

Environmental Engineer

Las Vegas, NV · On-site +1

We are open to remote candidates. In this role, the Environmental Engineer is responsible for ... Ensure all required EHS permits are current, accurate, and maintained for operational compliance

New

Ocean Spray

Environmental Engineer

Chicago, IL · On-site +1

We are open to remote candidates. In this role, the Environmental Engineer is responsible for ... Ensure all required EHS permits are current, accurate, and maintained for operational compliance

New

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Remote Ehs Analyst information

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$72.2K

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How much do remote ehs analyst jobs pay per year?

As of Jun 15, 2026, the average yearly pay for remote ehs analyst in the United States is $72,221.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,500.00 and $92,000.00 per year, depending on experience, location, and employer.

What does a Remote EHS Analyst do?

A Remote EHS (Environmental, Health, and Safety) Analyst monitors and ensures workplace compliance with environmental and safety regulations from a remote location. They analyze data, prepare reports, and provide recommendations to improve safety and environmental practices. Their duties often include conducting virtual audits, training employees online, and staying updated on relevant laws and standards. This role enables organizations to maintain high safety and environmental standards, even when on-site presence is limited.

What are some unique challenges faced by Remote EHS Analysts when ensuring compliance across multiple locations?

Remote EHS Analysts often encounter the challenge of maintaining consistent safety standards and compliance across various sites, each with its own local regulations and operational nuances. Effective communication and collaboration with on-site teams are crucial, as analysts must rely on digital tools to monitor, audit, and train rather than being physically present. Building strong relationships with local staff and leveraging technology for virtual inspections and reporting can help overcome these barriers. Staying organized and proactive in following up on action items is key to success in this remote role.

What are the key skills and qualifications needed to thrive as a Remote EHS Analyst, and why are they important?

A Remote EHS Analyst typically needs a solid background in environmental health and safety regulations, risk assessment, and incident investigation, often supported by a relevant degree or certification such as CSP or CIH. Familiarity with EHS management software, data analysis tools, and regulatory compliance systems is essential for effective remote monitoring and reporting. Strong attention to detail, communication skills, and the ability to work independently are crucial soft skills for success in a remote setting. These competencies ensure regulatory compliance, workplace safety, and efficient management of environmental and safety risks across distributed locations.

What is the difference between Remote Ehs Analyst vs Remote Environmental Specialist?

AspectRemote Ehs AnalystRemote Environmental Specialist
Required CredentialsEnvironmental or EHS certifications, degree in environmental science or related fieldSimilar certifications, environmental science degree often preferred
Work EnvironmentPrimarily office-based, remote work, data analysis, compliance reportingRemote or field-based, site assessments, environmental monitoring
Employer & Industry UsageUsed across manufacturing, construction, corporate sectorsCommon in environmental consulting, government agencies, corporate sustainability

The Remote Ehs Analyst and Remote Environmental Specialist roles share many credentials and industry usage, but differ mainly in focus. The Ehs Analyst emphasizes compliance reporting and data analysis remotely, while the Environmental Specialist often involves site assessments and fieldwork. Both roles are vital in environmental management but cater to different operational needs.

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Remote Ehs Analyst jobs near you
Regulatory Analyst - Remote

Regulatory Analyst - Remote

University of Miami

Miami, FL • On-site, Remote

Full-time

Medical, Dental

Posted yesterday

University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

216th of 537 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/UHealth Department of SCCC has an exciting opportunity for a Full Time Regulatory Analyst 1 to work at the UHealth campus in Miami, Fl.

CORE JOB SUMMARY
The Regulatory Analyst 1 - UHealth conducts on-site audits and reviews consolidated records. The incumbent designs, reviews, and tests the revised treatment matrix to identify possible cancers from claims data.
CORE JOB FUNCTIONS

  • Analyzes regulatory requirements, identifies potential conflicts, and demonstrates thorough knowledge of federal regulations and University policies.

  • Oversees accurate and timely processing, tracking, and filing of federally mandated submissions.

  • Assists with the drafting, preparation, and presentation of programs to investigators and their research staff to raise awareness of research compliance.

  • Provides support to investigators by reviewing submissions for content.

  • Sends decision correspondence to appropriate parties, requesting information.

  • Maintains accurate databases and generates letters.

  • Develops and maintains templates, creates files, and mails notices.

  • 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 required
Experience: Minimum 1 year of relevant experience required
Knowledge, Skills and Abilities:

  • Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.

  • Teamwork: Ability to work collaboratively with others and contribute to a team environment.

  • Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.

  • Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.

Department Specific Functions

Job duties will include, but not be limited to:

Prepare and coordinate the entire process of regulatory document submission to the Institutional Review Board (IRB) from study start-up to study closure, including communicating with ancillary committees, study team, business office, contract research organizations, and sponsors.

Completion of the new protocol submission packet with the information provided by PRMC as well as any additional required documentation (i.e., local protocol, HIPAA forms, etc.). Modifying and standardizing consent forms for IRB submission is required.

Compilation of documents in order to prepare the following forms for IRB submission to ensure protocol compliance with federal regulations. This process will take place from study start-up throughout the completion of the study.

  • Initial IRB application

  • Amendments / modifications

  • Reportable new information

  • Protocol deviations / violations

  • Protocol exceptions

  • IND safety letters

  • Continuing and final reports

  • Other communications from the sponsor requiring IRB submission.

Preparation and maintenance of regulatory binders (paper or electronic) with all necessary study documentation in compliance with institutional standard operating procedures (SOPs), sponsor requirements (as applicable) and applicable regulatory requirements.

Communication with study staff to ensure the maintenance and accuracy of the Delegation of Authority Log (DOAL). Ensure in conjunction with the DOAL that all protocol-related training (whether initial or with a new study protocol amendment/modification) is completed for all study personnel and documentation maintained within the regulatory binder.

Maintains department credentialing information and research records for clinical trials within institution's electronic systems (e.g., Velos, Complion) and appropriate drives, as applicable.

Participate in site visits with monitors as well as site audits concerning compliance of regulatory documents. Ensure timely resolution of observations identified during monitoring and auditing visits.

Communicate with Clinical Coordinators and PIs to review and submit protocol deviations and amendments as part of the plan to resolve the deficiencies identified during the audit/monitoring visit.

Assist in the collection and maintenance of credentialing information for study personnel (e.g., study-specific training, IBC, EHS requirements, etc.).

Upkeep of departmental trackers with study updates to ensure study team personnel are effectively alerted of initial study approvals and IRB approved study and consent amendments.

Communicate to SCCC staff and PI relevant aspects of the regulatory process concerning IRB approval of initial protocol, exceptions, continuing reports, and study modifications. This includes facilitation of training and notification of required re-consenting in collaboration with the clinical team following approval of study modifications.

Provides updates to the study team and/or management regarding submission statuses and approvals (e.g. initial and amendments) during internal team meetings and upon request.

Communicate with the sponsor and/or contract research organization for completion and submission of regulatory documents via inter-links, regular mail, or email as well as provide submission updates upon request. This responsibility is sponsor dependent. The following documents may be included:

  • Financial Disclosure Forms

  • FDA 1572

  • Initial Protocol Signature Page

  • Amendments signature page

  • Investigators CV and Medical Licenses

  • Laboratories normal ranges and certifications

  • IRB approvals

  • Approved consents

  • Other documents as required by the sponsor

Provide feedback to Regulatory Management on opportunities for regulatory process improvement.

Identifies and escalates issues before they become critical.

Assists with various regulatory related projects under the direction of the Regulatory Manager and/or Director of Regulatory.

Other duties as assigned by senior management.

Education:

  • Bachelor's degree required

  • Any relevant education, certifications and/or work experience may be considered.

Experience:

  • Minimum one (1) year of relevant experience in compliance, research, or a medical setting.

  • Experience in clinical trials is preferred.

#LI-YC1

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

Sourced by ZipRecruiter

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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