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Study Management Associate Jobs in Wadsworth, IL

We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ... Perform routine and complex imaging studies, manage PACS submissions, and ensure all patient data ...

Coordinate with sales management to ensure market engagement is completed on a timely basis ... Help create product collateral (e.g., brochures, case studies, product videos, website copy) to ...

Sonography Tech

Hoffman Estates, IL · On-site

$56 - $58/hr

Perform routine and complex imaging studies, manage PACS submissions, and ensure all patient data ... We empower our 97,000+ associates to bring their skills and expertise every day to reimagining ...

Interact with outside Sales Territory Managers, Area Sales Managers, Inside Sales Reps, Supply ... Studies have shown people are less likely to apply to jobs unless they meet every single ...

Showing results 21-40

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 cities near Wadsworth, IL are hiring for Study Management Associate jobs?

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

Infographic showing various Study Management Associate job openings in Wadsworth, 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, Central Monitor - Hybrid

Initial Therapeutics, Inc.

North Chicago, IL • On-site

$120 - $160/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago


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 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.

**This is a hybrid based role working on‑site T‑TH. Candidates must be local to Lake County, IL or Irvine, CA and work on‑site 3 days a week.**

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.
Qualifications
  • Education & Experience
    • Bachelors degree in related field, may include life sciences, risk‑based discipline.
    • Minimum of 10 years of clinically related experience or data trend analysis experience, at least 5 years 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).
Additional Information
  • Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
    The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short‑term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company’s sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

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

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