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Argus Jobs in Chicago, IL (NOW HIRING)

Cushman & Wakefield

Senior Associate

Chicago, IL

This position requires significant computer and communication skills with a strong emphasis on ARGUS and Excel modeling. Desire to work across multiple property types, professionalism, and attention ...

Pacificlife

Real Estate Associate

Oak Park, IL · On-site +1

Create/modify complex cash flow models in Argus and Excel for commercial and multifamily properties. * Organize and support analysis, draw objective conclusions. * Present verbal and written ...

Newcastle Investors

Analyst

Chicago, IL

Prepare financial models (Excel, Argus, etc.) to analyze investments, model project capitalization, perform sensitivity analyses, and pitch investment opportunities to capital partners. * Market ...

Colliers

Senior Financial Analyst

Rosemont, IL · On-site

$90K - $114K/yr

Underwrite income-producing assets using ARGUS and Excel, including 10-year cash flow projections and key metrics (IRR, NPV, cap rates, NER) * Analyze lease proposals and buy vs. lease scenarios ...

Ryan Companies

Capital Markets Associate

Chicago, IL · On-site +1

$120K - $150K/yr

Develop a strong working knowledge of Argus and other relevant real estate software. * Assist in managing the sale process of Ryan investment properties, including coordinating with brokers and ...

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$88

How much do argus jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for argus in Chicago, IL is $50.62, according to ZipRecruiter salary data. Most workers in this role earn between $39.62 and $57.21 per hour, depending on experience, location, and employer.

What are the typical day-to-day responsibilities of an Argus Safety Specialist?

As an Argus Safety Specialist, your daily tasks often include case processing and data entry in the Argus Safety database, reviewing and coding adverse event reports, and ensuring timely submission of safety information to regulatory authorities. You may also coordinate with clinical teams, medical reviewers, and regulatory affairs professionals to resolve case queries and clarify data. This role may involve periodic training updates or process improvement activities. Strong organizational skills and an ability to manage multiple cases concurrently are essential for success, as timeliness and accuracy directly impact compliance and patient safety.

What skills and qualifications are needed for an Argus?

To thrive as an Argus Safety Specialist, you need a strong background in pharmacovigilance, regulatory reporting, and a relevant life sciences degree. Proficiency with Argus Safety database software, strong familiarity with compliance standards, and in some cases, certifications such as Drug Safety Certification or GVP training, are commonly required. Attention to detail, analytical thinking, and effective communication skills distinguish top performers in this field. These competencies ensure accurate data handling, timely regulatory reporting, and clear collaboration with cross-functional teams, which are vital in pharmaceutical safety operations.

What is an Argus?

An Argus job typically refers to roles involving the use of Argus software, which is widely used for financial modeling, asset management, and real estate investment analysis. Professionals in this role analyze financial data, generate forecasts, and support decision-making in industries such as commercial real estate and investment management. Common positions include financial analysts, asset managers, and real estate consultants. Strong analytical skills and proficiency in Argus software are essential for success in this field.

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What job categories do people searching Argus jobs in Chicago, IL look for? The top searched job categories for Argus jobs in Chicago, IL are:
Argus jobs near you
Infographic showing various Argus job openings in Chicago, IL as of August 2026, with employment types broken down into 92% Full Time, 5% Part Time, 2% Contract, and 1% Summer. Highlights an 85% Physical, 8% Hybrid, and 7% Remote job distribution, with an average salary of $105,298 per year, or $50.6 per hour.

Senior Pharmacovigilance System Architect (Argus Administrator) - US

MMS

Chicago, IL • On-site

Full-time

Posted 28 days ago

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

Senior Pharmacovigilance System Architect

We are recruiting for an experienced Pharmacovigilance System Architect (Argus Administrator SME) to join our US team.

Roles & Responsibilities

  • Serves as Database Administrator for Argus Safety, including database configuration, issue resolution, maintenance, governance and daily support.
  • Performs installations, upgrades, configuration of reporting rules, and E2B reporting via gateway technologies (including set-up and configuration of Axway Gateway Interchange).
  • Provides support for all systems associated with PV and drug safety.
  • Performs updates to Argus configuration and processes as per changing EudraVigilance regulations.
  • Provides support and execution of activities related to EudraVigilance testing for various clients.
  • Performs case migration/database transfers, file importing and supports other case processing activities.
  • Provides leadership in executing Argus upgrades and related activities.
  • Provides administrator support for other safety databases (such as ARISg).
  • Performs periodic coding dictionary (MedDRA & WHO drug) updates for Argus.
  • Provides technical assistance and support to Drug Safety Associate team with electronic submissions of serious adverse advents to European agencies.
  • Writes procedural documents including Standard Operating Procedures (SOP), Work Practice Documents, and Data Entry Manuals for Argus Safety.
  • Generates case processing metrics, reviews and makes suggestions and supports process improvement implementation.
  • Maintains technical expertise of regulatory requirements and ensures alignment with company working practices.
  • Assists with business development and capabilities efforts as needed.
  • Interacts directly and independently with client to coordinate all facets of projects; competent communicator, supports client capabilities as PV/drug safety systems SME.
  • Strong understanding and experience working with Argus configuration and study set up.
  • Strong understanding of global case processing and SAE reporting.
  • Strong understanding of global clinical trial development and data.

Requirements

  • College graduate Information Technology discipline or related field, or relevant experience.
  • Minimum of 5 years’ experience in Information Technology or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Reputation as emerging leader in field with sustained performance and accomplishment.
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Excellent problem-solving skills.
  • Good organizational and communication skills.
  • Familiarity with current ISO 9001 and ISO 27001 standards preferred.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

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M. M. S. logo

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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