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Study Management Associate Jobs in North Chicago, IL

Flexport

Trucking Pricing Associate

Chicago, IL

In this role you will manage pricing requests, bids, and formal RFPs across Drayage, Cartage/LTL ... Conduct complex network studies based on volume flows, strategic priorities and market trends to ...

WPP Media

Associate Director, Pitch

Chicago, IL · On-site

You will be instrumental in driving project timelines, managing deliverables, and ensuring the ... Read and understand content and case studies that contribute to the overall pitch narrative.

WPP Media

Associate Director, Pitch

Chicago, IL · On-site

You will be instrumental in driving project timelines, managing deliverables, and ensuring the ... Read and understand content and case studies that contribute to the overall pitch narrative.

WPP Media

Associate Director, Pitch

Chicago, IL · On-site

You will be instrumental in driving project timelines, managing deliverables, and ensuring the ... Read and understand content and case studies that contribute to the overall pitch narrative.

National Safety Council

Research Associate

Itasca, IL · On-site

$65K - $72K/yr

Designs and executes components of research studies and program evaluations; collects, analyzes ... Collect, manage, and analyze quantitative and qualitative data using appropriate statistical and ...

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Study Management Associate information

What is a study management associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.

What are the typical responsibilities of a study management associate?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What are the key skills and qualifications needed to thrive as a study management associate?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are popular job titles related to Study Management Associate jobs in North Chicago, IL?

For Study Management Associate jobs in North Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Study Management Associate jobs in North Chicago, IL look for?

The top searched job categories for Study Management Associate jobs in North Chicago, IL are:

What cities near North Chicago, IL are hiring for Study Management Associate jobs?

Cities near North Chicago, IL with the most Study Management Associate job openings:

Study Management Associate jobs near you
Infographic showing various Study Management Associate job openings in North Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Associate Director/Director of Toxicology

Frontage Laboratories, Inc.

Chicago, IL • On-site

$140 - $160/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 20 days ago

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Associate Director/Director of Toxicology

Full Time Chicago, IL, US

3 days ago Requisition ID: 1840

Salary Range: $140,000.00 To $160,000.00 Annually

Job Title: Associate Director/Director of Toxicology. Location: Chicago, IL. Reports to: Vice President of Safety and Toxicology. Full-time.

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, Europe, and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Our Chicago, IL site provides services in general toxicology, developmental and reproductive toxicology (DART), juvenile and ocular toxicology in support of pharmaceutical and biotechnology products.

Position Summary

Frontage Laboratories is seeking an experienced and highly motivated Director of Toxicology with specialized expertise in Developmental and Reproductive Toxicology. This leadership role will be responsible for overseeing study design, execution, and interpretation of nonclinical toxicology studies, while managing and mentoring a team of scientists. The ideal candidate will bring strong scientific expertise, regulatory knowledge, and proven leadership experience within a CRO environment.

Key Responsibilities
  • Lead and oversee General Tox, Developmental and Reproductive Toxicology studies in compliance with GLP and regulatory guidelines
  • Provide scientific direction for study design, protocol development, and data interpretation
  • Serve as Study Director, as and when needed, or Senior Scientific Advisor on complex programs
  • Manage, mentor, and grow a team of Study Directors and scientific staff
  • Ensure high-quality deliverables, timelines, and client satisfaction
  • Interact with clients to provide scientific guidance and support business development efforts
  • Contribute to regulatory submissions and support audits/inspections (FDA, OECD, etc.)
  • Stay current with evolving regulatory requirements and scientific advancements
Qualifications
  • PhD in Toxicology or a related field
  • 5–7 years of relevant experience in a reputable CRO or pharmaceutical/biotech setting
  • Demonstrated expertise in reproductive and developmental toxicology study design and interpretationExperience serving as Study Director in GLP‑compliant studies
  • Proven experience managing and leading scientific teams
  • Strong knowledge of regulatory guidelines (FDA, ICH, OECD)
  • Excellent communication, leadership, and client‑facing skills
Preferred Qualifications
  • Board certification (e.g., DABT) is a plus
  • Track record of successful client engagement and project delivery
Salary

$140-160k, based upon experience.

  • 401k Employer Match with immediate vesting
  • Vision Insurance
  • Medical and Dental Insurance with multiple coverage options
  • FSA (Medical, Dependent Care, and Commuter)
  • Short Term Disability
  • Long Term Disability
  • Life Insurance
  • Generous Paid Holidays and PTO

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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