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Study Management Associate Jobs in Chicago, IL (NOW HIRING)

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

... Study brand standards. Our caring and attentive associates reinforce our principal belief that ... A Bachelor's degree in Business Administration, Hotel Management, or related field is preferred.

As a Senior Associate, you will build meaningful client connections and learn how to manage and ... study: Management Information Systems, Computer and Information Science, Systems Engineering ...

... Study brand standards. Our caring and attentive associates reinforce our principal belief that ... A Bachelor's degree in Business Administration, Hotel Management, or related field is preferred.

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Manage research data and monitor study health -- Pull, organize, and QC research datasets; maintain documentation standards and support data integrity for active studies; build and maintain ...

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In partnership with the Housekeeping Manager, ensure that we deliver a comfortable and clean guest experience and align with Study brand standards. Our caring and attentive associates reinforce our ...

In partnership with the Housekeeping Manager, ensure that we deliver a comfortable and clean guest experience and align with Study brand standards. Our caring and attentive associates reinforce our ...

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Bartender

Chicago, IL · On-site

$19.57/hr

Our caring and attentive associates reinforce our principal belief that guest service is our ... Study Hotels is a drug-free workplace. Pre-employment drug test and background check required.

Our caring and attentive associates reinforce our principal belief that guest service is our ... Study Hotels is a drug-free workplace. Pre-employment drug test and background check required.

New

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The Study at University of Chicago is currently seeking a full-time Guest Service Agent to provide ... Our caring and attentive associates reinforce our principal belief that guest service is our ...

Our caring and attentive associates reinforce our principal belief that guest service is our ... Study Hotels is a drug-free workplace. Pre-employment drug test and background check required.

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Study Management Associate information

What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?

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 the typical responsibilities of a Study Management Associate in a clinical research team?

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 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 job categories do people searching Study Management Associate jobs in Chicago, IL look for? The top searched job categories for Study Management Associate jobs in Chicago, IL are:
What cities near Chicago, IL are hiring for Study Management Associate jobs? Cities near Chicago, IL with the most Study Management Associate job openings:
Infographic showing various Study Management Associate job openings in Chicago, IL as of June 2026, with employment types broken down into 87% Full Time, and 13% Part Time. Highlights an 87% In-person, 9% Hybrid, and 4% Remote job distribution.
Associate Director, Central Monitor - Hybrid

Associate Director, Central Monitor - Hybrid

AbbVie

North Chicago, IL • On-site

Full-time

Posted 17 days ago


AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 97 frontline employees who took The Breakroom Quiz

13th of 73 rated pharmaceutical


Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Central Monitoring Associate Director is responsible for bringing science to life by leading a cross-functional team of Central Monitoring Managers charged with de-risking assigned clinical studies and thereby advancing AbbVie clinical research and development programs. The Central Monitoring Associate Director is accountable for service delivery results (quality, efficient, on-time and on-objective delivery) and for the building and strengthening the talent pipeline for today's needs and for the leaders of tomorrow.
The Associate Director of Central Monitoring role is a manager of manager position that will be filled when organizational size requires this level to manage span of control.

Responsibilities:

  • Responsible for maximizing the value and efficiently utilizing AbbVie's most valuable resource (staff) in the front-line Central Monitoring space. Leads, manages, and supervises a combined team of Central Monitoring Managers with delivery responsibilities for a portfolio of studies.
  • Creates an internal leadership talent pipeline and mentors/coaches team members on their leadership journey
  • Fosters a growth mindset within the team based on inclusive collaboration, innovation, learning and continuous improvement that delivers successful outcomes for the study, the team, the individual and the business.
  • Develops the central monitoring staffing strategy and tactics in support of assigned clinical research programs, to ensure execution is with quality and efficiency, on-time, and in line with company objectives.
  • Executes and manages the central monitoring staffing strategy including fluidly adjusting plans in support of project priorities and/or timelines plan.
  • Recruits, hires, and trains the front-line Central Monitoring Leadership team, including therapeutic area training, compliance training and study management-specific knowledge as required to perform assigned tasks.
  • Manages the performance cycle including expectation setting, objective setting (both tactical and stretch opportunities to ensure continuous growth), the provision of constructive and timely feedback (informal & formal, direct feedback as well as feedback from CDO business partners) reviews and management of any performance issues to resolution.
  • Interacts with and influences all levels of management and cross-functional team members in Clinical Development Operations to achieve high standards of output from front-line Central Monitoring Leadership staff.

**This is a hybrid based role working on-site T-TH. Candidates must be local to Marlow,  and work on-site 3 days a week. 

Qualifications
  • Education & Experience
    Bachelors degree in related field, may include life sciences, risk-based discipline.
    Extensive clinically related experience or data trend analysis experience, and people management experience (remote experience preferred).
    Experience working in an RBQM-model or similar experience with risk-based monitoring required.
    Experience/exposure to drug development, operations, risk management, successful decision-making, strategic execution
  • Make Possibilities Real
    Proven leadership skills in a cross-functional global team environment.
    Experience in managing remote/virtual teams and an ability to influence and align stakeholders, while modeling and driving AbbVie's leadership attributes.
    Ability to remove obstacles and provide support that enables direct reports to achieve results.
    Able to successfully coach and mentor both with direct reports and in a matrix environment.
  • Clear & Courageous
    Respectfully provides transparent, accurate and timely feedback to help direct reports improve performance.
  • Analytic & Critical Thinking Skills
    Strong analytical and critical thinking skills and the ability to evaluate complex issues from multiple perspectives and drive SMART SURE decision making and timely outcomes.
    Ability to anticipate and address critical issues; and develop contingency plans in a proactive manner.
  • Interpersonal & Communication Skills
    Acts with integrity in accordance with ABBVIE code of business conduct.
    Evangelist for RBQM within the organization, promoting value of early detection in de-risking studies.
    Strong English language skills-spoken, written, and conversational.
    Lead dynamic meetings and create engaging presentations.
  • Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility, and adaptability to changing requirements, resourcefulness, and creativity. Demonstrated proactive and positive team player.
    Able to maintain calm, cool, collected, and competent composure in high pressure situations in order to ensure successful hand-off to stakeholders responsible for taking action.
    Open and receptive to the gift of feedback in the pursuit of continuous improvement.
  • Organizational Skills
    Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadlines.
  • Computer Skills
    Comfortable with use/operation of data analytics and visualization tools for oversight.
    Competent with Microsoft Office applications (Outlook, Word, Excel, PowerPoint, and Teams).

GRADE AND BENEFITS WILL DEPEND ON LOCAL COUNTRY 

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html


What AbbVie employees say

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Benefits

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AbbVie logo

About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013