Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
Quick apply
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
Quick apply
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
North Chicago, IL · On-site
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
North Chicago, IL · On-site
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
North Chicago, IL · On-site
$141K/yr
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
North Chicago, IL · On-site
$141K/yr
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
Responsibilities: • Independently manage and monitor approximately 1-2 high-volume clinical study sites, serving as a primary point of contact between Abbott and assigned sites. • Conduct ...
Responsibilities: • Independently manage and monitor approximately 1-2 high-volume clinical study sites, serving as a primary point of contact between Abbott and assigned sites. • Conduct ...
Chicago, IL · On-site
$25 - $33.25/hr
Responsibilities Research Conduct/Study Management: * Manages multiple moderately complex clinical trials that may include national level and multi-institutional pharmaceutical. * Recruits and ...
Chicago, IL · On-site
$25 - $33.25/hr
Responsibilities Research Conduct/Study Management: * Manages multiple moderately complex clinical trials that may include national level and multi-institutional pharmaceutical. * Recruits and ...
North Chicago, IL · On-site
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
North Chicago, IL · On-site
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
Chicago, IL · On-site
$25 - $33.25/hr
Responsibilities Research Conduct/Study Management: * Manages multiple moderately complex clinical trials that may include national level and multi-institutional pharmaceutical. * Recruits and ...
Chicago, IL · On-site
$25 - $33.25/hr
Responsibilities Research Conduct/Study Management: * Manages multiple moderately complex clinical trials that may include national level and multi-institutional pharmaceutical. * Recruits and ...
Chicago, IL · On-site
$60 - $75/hr
Research Conduct/Study Management:* Manages multiple moderately complex clinical trials that may include national level and multi-institutional pharmaceutical.* Recruits and screens study subjects ...
Chicago, IL · On-site
$60 - $75/hr
Research Conduct/Study Management:* Manages multiple moderately complex clinical trials that may include national level and multi-institutional pharmaceutical.* Recruits and screens study subjects ...
Chicago, IL · On-site
$90 - $130/hr
... clinical trials management, and community outreach and engagement. The UCCCC has one of the largest ... Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating ...
Chicago, IL · On-site
$90 - $130/hr
... clinical trials management, and community outreach and engagement. The UCCCC has one of the largest ... Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating ...
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. * Author regulatory documents including protocols, study reports ...
Quick apply
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. * Author regulatory documents including protocols, study reports ...
North Chicago, IL · On-site
$109K/yr
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. * Author regulatory documents including protocols, study reports ...
North Chicago, IL · On-site
$109K/yr
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. * Author regulatory documents including protocols, study reports ...
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. * Author regulatory documents including protocols, study reports ...
Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy. * Author regulatory documents including protocols, study reports ...
North Chicago, IL · On-site
$150 - $200/hr
... Study reports, regulatory submissions and responses, and other program documents. * Manages one level of Medical and Scientific Directors (typically 2 to 4) and/or Clinical Scientists. This ...
North Chicago, IL · On-site
$150 - $200/hr
... Study reports, regulatory submissions and responses, and other program documents. * Manages one level of Medical and Scientific Directors (typically 2 to 4) and/or Clinical Scientists. This ...
Chicago, IL · On-site
... clinical trials management, and community outreach and engagement. The UCCCC has one of the largest ... Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating ...
Chicago, IL · On-site
... clinical trials management, and community outreach and engagement. The UCCCC has one of the largest ... Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating ...
Chicago, IL · On-site
... clinical trials management, and community outreach and engagement. The UCCCC has one of the largest ... Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating ...
Chicago, IL · On-site
... clinical trials management, and community outreach and engagement. The UCCCC has one of the largest ... Many of these studies are investigator-initiated, including Phase I or I/II trials, demonstrating ...
North Chicago, IL · On-site
$109K/yr
Author regulatory documents including protocols, study reports, population PK reports, exposure ... Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a ...
North Chicago, IL · On-site
$109K/yr
Author regulatory documents including protocols, study reports, population PK reports, exposure ... Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a ...
Chicago, IL · On-site
$71K - $89K/yr
Develop and implement study procedures, maintains study records, tracks study progress, and ... Strong data management skills and attention to detail. * Excellent time management and ability to ...
Chicago, IL · On-site
$71K - $89K/yr
Develop and implement study procedures, maintains study records, tracks study progress, and ... Strong data management skills and attention to detail. * Excellent time management and ability to ...
North Chicago, IL · On-site
Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical/ preclinical studies. * Apply experience to analyze ...
North Chicago, IL · On-site
Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical/ preclinical studies. * Apply experience to analyze ...
Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical/ preclinical studies. * Apply experience to analyze ...
Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical/ preclinical studies. * Apply experience to analyze ...
North Chicago, IL · On-site
$120 - $180/hr
Author regulatory documents including protocols, study reports, population PK reports, exposure ... Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a ...
North Chicago, IL · On-site
$120 - $180/hr
Author regulatory documents including protocols, study reports, population PK reports, exposure ... Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a ...
$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 Study Startup Manager | Clinical Research Coordinator |
|---|---|---|
| Responsibilities | Oversees study initiation, site selection, regulatory submissions, and startup activities | Manages participant recruitment, data collection, and day-to-day study operations at sites |
| Required Credentials | Bachelor's degree, clinical research experience, knowledge of regulations | Bachelor's degree, clinical research experience, good clinical practice (GCP) training |
| Work Environment | Corporate or sponsor offices, clinical trial sites | Clinical trial sites, hospitals, research centers |
The Clinical Study Startup Manager focuses on preparing and initiating clinical trials, ensuring regulatory compliance and site readiness. In contrast, the Clinical Research Coordinator handles the daily operations at trial sites, managing participant interactions and data collection. Both roles require similar credentials and work in related environments, but their core responsibilities differ significantly.
The most popular types of Clinical Study Startup jobs in Park Ridge, IL are:
The top searched job categories for Clinical Study Startup Manager jobs in Park Ridge, IL are:
Cities near Park Ridge, IL with the most Clinical Study Startup Manager job openings:

North Chicago, IL
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 9 days ago
8.7
Based on 103 frontline employees who took The Breakroom Quiz
14th of 86 rated pharmaceutical
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 DescriptionPurpose:
Conceives, executes and effectively manages and communicates multi-disciplinary Clinical Pharmacology development plans and strategies that achieve commercial goals and regulatory requirements for multiple functions. Generates new PK/PD study proposals and leads those efforts. Anticipates and critically evaluates Clinical Pharmacology, PK/PD or regulatory advances, strengths, weaknesses, opportunities and threats, and responds with appropriate new strategies. Consistently demonstrates excellent record of accomplishment of Clinical Pharmacology and business objectives. Leads Clinical Pharmacology/PK/PD aspects of multiple projects. Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management.
Responsibilities:
This position can be hired based on the below qualifications:
Associate Director, Clinical Pharmacology
Senior Clinical Pharmacologist:
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
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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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.
Scientific research and development services
10,000+ Employees
North Chicago, IL, US
2013