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Interpretive Guide Jobs in Chicago, IL (NOW HIRING)

MMS

Senior Medical Writer (Remote)

Chicago, IL · On-site

Contribute substantially to, or manages, production of interpretive guides * Take ownership of a given assignment, proactively consulting other project team members and other department ...

AAAHC

Standards Program Development Manager

Deerfield, IL · On-site

$80K - $110K/yr

Apply AAAHC Standards development principles, policies, style guides, and architectural frameworks (including taxonomy, weighting and scoring methodologies, interpretive guidance, applicability ...

Cantigny

Education Manager

Wheaton, IL

$75K - $85K/yr

Create age-appropriate, inquiry-based interpretive experiences that support critical thinking ... Develop facilitation guides, lesson plans, and educator toolkits. * Build and maintain a ...

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All JobsInterpretive Guide JobsInterpretive Guide Jobs in Chicago, IL

Interpretive Guide information

See Chicago, IL salary details

$6

$17

$25

How much do interpretive guide jobs pay per hour?

As of Aug 1, 2026, the average hourly pay for interpretive guide in Chicago, IL is $17.10, according to ZipRecruiter salary data. Most workers in this role earn between $12.34 and $19.74 per hour, depending on experience, location, and employer.

What are some common challenges Interpretive Guides face when engaging diverse audiences, and how can they overcome them?

Interpretive Guides often encounter groups with varying ages, backgrounds, and interests, which can make it challenging to keep everyone engaged. To overcome this, guides typically use a mix of storytelling, interactive activities, and adaptive communication techniques to connect with different learning styles. Flexibility and strong observation skills are key, allowing guides to adjust their approach on the spot for maximum impact. Building rapport and encouraging questions also helps ensure that all visitors feel included and engaged throughout the experience.

What are interpretive guides?

Interpretive guides are professionals who lead visitors through parks, museums, historical sites, or natural areas, providing educational and engaging information about the location’s natural, cultural, or historical significance. They use storytelling, demonstrations, and interactive activities to help guests connect with and understand the subject matter. Interpretive guides often tailor their presentations to different audiences and play a key role in conservation and public education efforts.

What is the difference between Interpretive Guide vs Naturalist?

AspectInterpretive GuideNaturalist
CredentialsOften requires interpretive or environmental education certificationsTypically has naturalist or environmental science background, sometimes with certifications
Work EnvironmentGuides visitors, leads tours, educates the public in parks, museums, or nature centersConducts research, observes wildlife, educates about ecosystems, often in field settings
Employer & IndustryFound in parks, zoos, museums, eco-tourismFound in parks, research institutions, conservation organizations

While both roles focus on environmental education, Interpretive Guides primarily lead tours and engage visitors, whereas Naturalists often conduct research and provide in-depth ecological education. The roles overlap in credentials and work environments, but their primary focus and activities differ.

What are the key skills and qualifications needed to thrive as an Interpretive Guide, and why are they important?

To thrive as an Interpretive Guide, you need a solid understanding of natural or cultural history, excellent communication skills, and often a background in education or environmental science. Familiarity with audio-visual presentation tools, interpretive planning software, and certifications like Certified Interpretive Guide (CIG) are commonly required. Outstanding interpersonal skills, creativity, and the ability to engage diverse audiences set top guides apart. These skills are vital for delivering informative, memorable experiences that connect visitors with the site’s significance and foster stewardship.
What are popular job titles related to Interpretive Guide jobs in Chicago, IL? For Interpretive Guide jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Interpretive Guide jobs in Chicago, IL look for? The top searched job categories for Interpretive Guide jobs in Chicago, IL are:
Interpretive Guide jobs near you
Infographic showing various Interpretive Guide job openings in Chicago, IL as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 17% Part Time, 1% Temporary, and 5% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $35,569 per year, or $17.1 per hour.

Senior Medical Writer (Remote)

MMS

Chicago, IL • On-site

Full-time

Re-posted 8 days ago

Job description

About MMS
MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating.
Our mission is to deliver high-quality service and technology solutions – rooted in strong science and decades of regulatory experience – that will assist our clients in developing and marketing life-changing therapies to positively improve lives worldwide.
MMS recognizes that a talented staff is what drives our business forward. Identifying and attracting top talent and continual training to strengthen core skills are essential to its core mission. At MMS, enthusiasm, collaboration, and teamwork are fostered, knowing that a global and diverse talent pool makes the company stronger. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
  • Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias
  • Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy summaries, Module 2.7.1, 2.7.2, 2.7.3, 2.7.4, and 2.5 documents, presentation materials and publications to medical journals
  • Complete writing assignments in a timely manner
  • Maintain timelines and workflow of writing assignments
  • Practice good internal and external customer service
  • Highly proficient with styles of writing for various regulatory documents
  • Expert proficiency with client templates & style guides
  • Interact directly and independently with client to coordinate all facets of projects; competent communicator skills for projects
  • Contribute substantially to, or manages, production of interpretive guides
  • Take ownership of a given assignment, proactively consulting other project team members and other department representatives for information or guidance as necessary
  • Mentor medical writers and other members of the project team who are involved in the writing process
Requirements
  • At least 3 years of previous experience in the pharmaceutical industry
  • Must have at least 3-5 years of industry regulatory writing and clinical medical writing experience
  • The ideal candidate would hold a Bachelors, Masters, or Ph.D. in scientific, medical, clinical discipline
  • Substantial clinical study protocol experience, as lead author, required
  • Experience leading and managing teams while authoring regulatory documents with aggressive timelines
  • Experience in regulatory submissions (clinical study reports) presented to regulatory authorities a plus
  • Understanding of clinical data
  • Exceptional writing skills are a must
  • Excellent organizational skills and the ability to multi-task are essential prerequisites
  • Candidate must be an expert in MS Word, Excel, PowerPoint, and related word processing tools
  • Experience being a project lead, or managing a project team
  • Strong understanding of federal regulations, Good Clinical Practices, and ICH guidelines a plus
  • Not required, but experience with orphan drug designations and PSP/PIPs a plus

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About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980

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