Chicago, IL · On-site
$60K - $65K/yr
As a Clinical Trials Coordinator, you'll work alongside experienced investigators, managing study operations from enrollment through completion while serving as a steady, trusted presence for ...
Chicago, IL · On-site
$60K - $65K/yr
As a Clinical Trials Coordinator, you'll work alongside experienced investigators, managing study operations from enrollment through completion while serving as a steady, trusted presence for ...
Tasks may include but are not limited to: Medically manages clinical trials to which s/he is assigned as MM Serves as Global Lead MM (GLMM) for pan-regional and/.or global trial(s) to which s ...
Tasks may include but are not limited to: Medically manages clinical trials to which s/he is assigned as MM Serves as Global Lead MM (GLMM) for pan-regional and/.or global trial(s) to which s ...
$25 - $33.25/hr
Strong organizational skills with the ability to manage multiple concurrent clinical trials and competing priorities. * Effective communication and interpersonal skills to serve as a reliable point ...
Quick apply
$25 - $33.25/hr
Strong organizational skills with the ability to manage multiple concurrent clinical trials and competing priorities. * Effective communication and interpersonal skills to serve as a reliable point ...
Chicago, IL · On-site
$71K - $89K/yr
Research certification (e.g., SoCRA, ACRP, Graham School Clinical Trials Management & Regulatory Compliance). * Fundamental working knowledge of clinical research. * Knowledge of clinical trials ...
Chicago, IL · On-site
$71K - $89K/yr
Research certification (e.g., SoCRA, ACRP, Graham School Clinical Trials Management & Regulatory Compliance). * Fundamental working knowledge of clinical research. * Knowledge of clinical trials ...
... trials. Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards. Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance ...
... trials. Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards. Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance ...
... trials. Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards. Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance ...
... trials. Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards. Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Chicago, IL · On-site
$136.80 - $167.20/hr
... case management while setting expectations for execution consistency. Lead site onboarding ... trials expand. Informally mentor and guide junior clinical specialists and cross‑functional ...
New
Chicago, IL · On-site
$136.80 - $167.20/hr
... case management while setting expectations for execution consistency. Lead site onboarding ... trials expand. Informally mentor and guide junior clinical specialists and cross‑functional ...
New
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Chicago, IL · On-site
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
Chicago, IL · On-site
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Chicago, IL · On-site
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
Chicago, IL · On-site
$80K - $100K/yr
Tempus created the TIME clinical trials network to increase patient access to clinical trials by ... We are looking for an experienced Study Start-Up Manager who will work with our cross- functional ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials. * Conduct ... Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC ...
$28.38 - $34.41
4% of jobs
$34.41 - $40.43
6% of jobs
$40.43 - $46.45
7% of jobs
$50.96 is the 25th percentile. Wages below this are outliers.
$46.45 - $52.47
9% of jobs
$52.47 - $58.49
15% of jobs
The median wage is $61.15 / hr.
$58.49 - $64.51
18% of jobs
$68.80 is the 75th percentile. Wages above this are outliers.
$64.51 - $70.53
21% of jobs
$70.53 - $76.55
7% of jobs
$76.55 - $82.57
6% of jobs
$82.57 - $88.59
3% of jobs
$88.59 - $94.62
2% of jobs
$28
$61
$94
| Aspect | Clinical Trials Manager | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Oversees entire clinical trial process, manages teams, ensures compliance, and handles budgets. | Assists with patient recruitment, data collection, and site coordination under supervision. |
| Required Credentials | Bachelor’s or higher in life sciences, often with project management experience. | Typically holds a bachelor’s degree in health sciences or related field; certification may be preferred. |
| Work Environment | Works in clinical trial sites, research organizations, or pharmaceutical companies. | Primarily works at clinical sites, hospitals, or research facilities. |
In summary, Clinical Trials Managers oversee the entire trial process and manage teams, while Clinical Research Coordinators support daily trial activities at the site level. Both roles require relevant education and work in clinical research settings, but differ in scope and responsibilities.
The most popular types of Clinical Trials jobs in Park Ridge, IL are:
The top searched job categories for Clinical Trials Manager jobs in Park Ridge, IL are:
Cities near Park Ridge, IL with the most Clinical Trials Manager job openings:
Chicago, IL • On-site
$60K - $65K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 18 days ago
Clinical Trials Coordinator - CNS & Behavioral Health
IMA Clinical Research | Chicago, IL Full-Time | $60,000-$65,000 annually
At IMA Clinical Research, we're advancing the science behind psychiatry, behavioral health, and central nervous system (CNS) conditions - work that directly shapes the treatment options available to patients tomorrow. As a Clinical Trials Coordinator, you'll work alongside experienced investigators, managing study operations from enrollment through completion while serving as a steady, trusted presence for participants navigating complex conditions.
If you thrive in a patient-facing environment and want your organizational skills to translate into real clinical progress, we encourage you to apply.
What You'll Be Doing
Required Qualifications
What We Offer
Become part of a team committed to expanding treatment options and improving lives through high-quality clinical research. Apply today.
The IMA Group is an Affirmative Action/Equal Opportunity Employer
Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
#LI-EG1 #LI-ONSITE
Employment Type: Full-Time
