Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
Responsible for critically evaluating technical and scientific aspects along with Clinical Pharmacology and Pharmacometrics management. Responsibilities: * Accountable for Phase 1-4 studies design ...
Associate Director, Clinical Pharmacology/Senior Clinical Pharmacologist (Oncology)
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 ...
Associate Director, Clinical Pharmacology/Senior Clinical Pharmacologist (Oncology)
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 ...
Associate Director, Clinical Pharmacology/ Senior Clinical Pharmacologist (Oncology)
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 ...
Associate Director, Clinical Pharmacology/ Senior Clinical Pharmacologist (Oncology)
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 ...
Clinical Research Coordinator II, Surgery
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 ...
Clinical Research Coordinator II, Surgery
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 ...
Associate Director, Clinical Pharmacology/ Senior Clinical Pharmacologist (Oncology)
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 ...
Associate Director, Clinical Pharmacology/ Senior Clinical Pharmacologist (Oncology)
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 ...
Clinical Research Coordinator II, Surgery
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 ...
Clinical Research Coordinator II, Surgery
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 ...
Clinical Research Coordinator II, Surgery
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 ...
Clinical Research Coordinator II, Surgery
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 ...
Clinical Research Manager
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 ...
Clinical Research Manager
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 ...
Senior Clinical Pharmacologist
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 ...
Senior Clinical Pharmacologist
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 ...
Head of Asset in GU, Oncology Clinical Development
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 ...
Head of Asset in GU, Oncology Clinical Development
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 ...
Clinical Research Manager
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 ...
Clinical Research Manager
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 ...
Clinical Research Manager
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 ...
Clinical Research Manager
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 ...
Senior Clinical Pharmacologist (Oncology)
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 ...
Senior Clinical Pharmacologist (Oncology)
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 ...
Clinical Research Nurse Coordinator
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 ...
Clinical Research Nurse Coordinator
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 ...
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing
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 ...
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing
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 ...
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing
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 ...
Senior Associate, Clinical Pharmacology Scientific Support & Reporting Writing
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 ...
Senior Clinical Pharmacologist (Oncology)
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 ...
Senior Clinical Pharmacologist (Oncology)
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 ...
Clinical Study Startup Manager information
See Park Ridge, IL salary details
$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
How much do clinical study startup manager jobs pay per hour?
What does a clinical study startup manager do?
What are the key skills and qualifications needed to thrive as a clinical study startup manager?
What are some common challenges faced by clinical study startup managers during the site activation process?
What is the difference between Clinical Study Startup Manager vs Clinical Research Coordinator?
| 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.
What are the most commonly searched types of Clinical Study Startup jobs in Park Ridge, IL?
The most popular types of Clinical Study Startup jobs in Park Ridge, IL are:
What job categories do people searching Clinical Study Startup Manager jobs in Park Ridge, IL look for?
The top searched job categories for Clinical Study Startup Manager jobs in Park Ridge, IL are:
What cities near Park Ridge, IL are hiring for Clinical Study Startup Manager jobs?
Cities near Park Ridge, IL with the most Clinical Study Startup Manager job openings:

Associate Director, Clinical Pharmacology/ Senior Clinical Pharmacologist (Oncology)
North Chicago, IL
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 10 days ago
AbbVie rating
8.7
Based on 103 frontline employees who took The Breakroom Quiz
14th of 86 rated pharmaceutical
Job 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 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:
- Accountable for Phase 1-4 studies design, and clinical pharmacology strategy; acts as the representative for project(s).
- Executes strategy, lead teams and various data analyses and interpretation by providing necessary context (including explaining MoA and disease specifics, available relevant internal and external data, analysis plans, interpretation and discussion of model results in the context of research question).
- Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports, CTDs, label sections, relevant section of investigator brochures, white papers, and other similar documents.
- Leads clinical pharmacology and biopharmaceutics meetings, serve as CLINICAL PHARMACOLOGY representative at Clinical Strategy Team/Asset Development Team and present at various departmental and cross functional teams such as study teams, CLINICAL PHARMACOLOGY leadership team, Journal club.
- Drives small teams with members from CLINICAL PHARMACOLOGY functional groups to provide a unified clinical pharmacology position to clinical, CMC and regulatory teams.
- Authors scientific publications and present at national and international conferences and interact with KOLs/external stakeholders.
- Conducts due diligence assessments, summarizes results and represents CLINICAL PHARMACOLOGY on business development teams.
- Represents Clinical Pharmacology at regulatory meetings.
This position can be hired based on the below qualifications:
Associate Director, Clinical Pharmacology
- PhD with typically 4+ years of experience or Pharm D with typically 6+ years of experience in a relevant field, Master’s Degree or equivalent education and typically 12+ years of experience, Bachelor’s Degree or equivalent education and typically 14+ years of experience;(*relevant field includes experience with PK, PBPK, PK-PD,Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
- Excellent interpersonal skills
- Ability to interact with functional representatives and KOLs externally and internally and lead team(s)
- Strategic thinking and enterprise view
- Proven scientific track record and technical skills to perform the role
- Key Leadership Competencies:
• Delivers business results while also positioning AbbVie for long-term success
• Persistent and resilient finds the way to move good ideas forward
• Acts respectfully yet courageously
• Connects unrelated concepts, generates original or unique ideas
• Influences colleagues to achieve cross-functional alignment
• Gives full accountability when delegating and accepts full accountability when delegated to by others
Senior Clinical Pharmacologist:
- PhD with 0 years of experience, or Pharm D with 2+ years of experience in a relevant field, Master’s Degree or equivalent education and typically 8+ years of experience, Bachelor’s Degree or equivalent education and typically 10+ years of experience; (*relevant field includes experience with PK, PBPK, PK-PD, Pharmacometrics or systems pharmacology, Drug metabolism/Transporters)
- Excellent interpersonal skills
- Ability to interact externally and internally and perform in a team setting
- Demonstrates scientific acumen and has technical skills to perform the role
- Key Leadership Competencies:
• Persistent and resilient finds the way to move good ideas forward
• Uses mistakes, failure and reflection as vehicles for learning and improvement
• Delivers business results while also positioning AbbVie for long-term success
• Connects unrelated concepts, generates original or unique ideas
• Influences colleagues to achieve cross-functional alignment
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 long-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
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