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 ...
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 ...
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 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 ...
Temporary Clinical Research Nurse Coordinator
Chicago, IL · On-site
$71K - $89K/yr
... and management of clinical trials. Under the direction of the PI, Co-Investigators, Advanced ... Develop and implement study procedures, maintains study records, tracks study progress, and ...
Temporary Clinical Research Nurse Coordinator
Chicago, IL · On-site
$71K - $89K/yr
... and management of clinical trials. Under the direction of the PI, Co-Investigators, Advanced ... Develop and implement study procedures, maintains study records, tracks study progress, and ...
Temporary Clinical Research Nurse Coordinator
Chicago, IL · On-site
$71K - $89K/yr
... and management of clinical trials. Under the direction of the PI, Co-Investigators, Advanced ... Develop and implement study procedures, maintains study records, tracks study progress, and ...
Temporary Clinical Research Nurse Coordinator
Chicago, IL · On-site
$71K - $89K/yr
... and management of clinical trials. Under the direction of the PI, Co-Investigators, Advanced ... Develop and implement study procedures, maintains study records, tracks study progress, and ...
Temporary Clinical Research Nurse Coordinator
Chicago, IL · On-site
$71K - $89K/yr
... and management of clinical trials. Under the direction of the PI, Co-Investigators, Advanced ... Develop and implement study procedures, maintains study records, tracks study progress, and ...
Temporary Clinical Research Nurse Coordinator
Chicago, IL · On-site
$71K - $89K/yr
... and management of clinical trials. Under the direction of the PI, Co-Investigators, Advanced ... Develop and implement study procedures, maintains study records, tracks study progress, and ...
Head of Asset in GU, Oncology Clinical Development
North Chicago, IL · On-site
$76K - $104K/yr
... 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 ...
Quick apply
Head of Asset in GU, Oncology Clinical Development
North Chicago, IL · On-site
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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
$248K/yr
... 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
$248K/yr
... 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 Coordinator
Addison, IL · On-site
$60K - $65K/yr
This position will report to the Clinical Site Manager. Main activities: • Recruit, screen and enroll clinical study participants. • Obtain proper written informed consent from each study ...
Clinical Research Coordinator
Addison, IL · On-site
$60K - $65K/yr
This position will report to the Clinical Site Manager. Main activities: • Recruit, screen and enroll clinical study participants. • Obtain proper written informed consent from each study ...
Author regulatory documents including protocols, study reports, population PK reports, exposure ... Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a ...
Quick apply
Author regulatory documents including protocols, study reports, population PK reports, exposure ... Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a ...
Head of Asset in GU, Oncology Clinical Development
North Chicago, IL · On-site
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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
$76K - $104K/yr
... 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 ...
Director, Clinical Affairs
Lincolnshire, IL · On-site
$168.49 - $264/hr
The Director, Clinical Affairs will be responsible for developing, coordinating, and executing the ... managing, and achieving project milestones with internal staff, other departments, and all study ...
Director, Clinical Affairs
Lincolnshire, IL · On-site
$168.49 - $264/hr
The Director, Clinical Affairs will be responsible for developing, coordinating, and executing the ... managing, and achieving project milestones with internal staff, other departments, and all study ...
Clinical Research Coordinator II - OBG - Research Staff
Chicago, IL · On-site
$25 - $33.25/hr
The Clinical Research Coordinator II independently manages and executes moderately complex clinical research studies from start up through close out. This role serves as a central operational lead ...
Clinical Research Coordinator II - OBG - Research Staff
Chicago, IL · On-site
$25 - $33.25/hr
The Clinical Research Coordinator II independently manages and executes moderately complex clinical research studies from start up through close out. This role serves as a central operational lead ...
Comply with the directives issued by the management regarding clinical studies. * Commit to producing work of the highest quality * Pay close attention to detail * Perform literature and competitive ...
Comply with the directives issued by the management regarding clinical studies. * Commit to producing work of the highest quality * Pay close attention to detail * Perform literature and competitive ...
Comply with the directives issued by the management regarding clinical studies. * Commit to producing work of the highest quality * Pay close attention to detail * Perform literature and competitive ...
Comply with the directives issued by the management regarding clinical studies. * Commit to producing work of the highest quality * Pay close attention to detail * Perform literature and competitive ...
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 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 does a clinical study startup manager do?
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:

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 17 days ago
AbbVie rating
8.6
Based on 101 frontline employees who took The Breakroom Quiz
16th 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.
Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical Pharmacology and Pharmacometrics (CPPM) goals. Generate new PK/PD proposals and lead those efforts. Investigate, identify, develop, and optimize new methods and techniques in PK/PD field. Act as a lead PK scientist in his/her area of expertise and critically evaluate relevant Clinical Pharmacology, PK/PD and regulatory advances and integrate this knowledge into research or development programs.
Responsibilities
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
- Contribute to clinical development by supporting Phase 1-4 studies including study design, and clinical pharmacology strategy.
- Author regulatory documents including protocols, study reports, population PK reports, exposure-response analyses reports, relevant section of investigator brochures, common technical documents, white papers, and other similar documents.
- Conduct data analyses including non-compartmental analyses, modeling and simulation, literature data analyses.
- Participate and present at various departmental and cross functional teams such as study teams, clinical pharmacology and biopharmaceutics, clinical strategy team, Clinical Pharmacology leadership team, Journal club.
- Collaborate with scientific support from other Clinical Pharmacology functional groups to provide a unified clinical pharmacology position to clinical, CMC and regulatory teams.
- Author scientific publications and present at scientific conferences.
- 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
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