Top 60 Clinical project manager Jobs in Deerfield, Il

R&D Manager, Clinical Research
Medline Industries —Northfield, IL
- $134,000 - $201,000 a year
- Full-time
- Hybrid work
- Nursing
- Office
- Bachelor's degree
- Health insurance
- 401(k)
Clinical Project Manager
Humboldt Park Health —Chicago, IL
- Microsoft Excel
- Mid-level
- Bachelor's degree
Quick Apply
Senior Clinical Project Manager
CEDENT —Chicago, IL
- 7 years
- Office
- Senior level
Software Project Manager
Siemens Healthineers —Schiller Park, IL
- $89,220 - $122,672 a year
- Full-time
- Current TB test
- Mid-level
- Criminal background check
- Disability insurance
- Health insurance
Program Implementation Manager, Clinical Studies
American Heart Association —Chicago, IL
- $70,000 - $90,000 a year
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Wellness program
- Paid holidays
8d
Project Manager – Doula Program & Women’s Health
Prism Health —Chicago, IL
- Weekends as needed
- Hybrid work
- Master of Social Work
- HIPAA
- Mid-level
Epidemiology Study Operations Manager
AbbVie —North Chicago, IL
- $109,500 - $208,500 a year
- Full-time
- Remote
- 6 years
- Windows
- Bachelor's degree
- Paid holidays
- Health insurance
8d
Clinical Data Management Specialist
Hollister Incorporated —Libertyville, IL
- $77,000 - $120,000 a year
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
- Paid holidays
- Disability insurance
Senior Manager, Clinical Quality Assurance
AbbVie —North Chicago, IL
- $124,500 - $236,500 a year
- Full-time
- Hybrid work
- Nursing
- 5 years
- Presentation skills
- Paid holidays
- Health insurance
Manager, Travel & Expense Program
Sysmex —Lincolnshire, IL
- $85,680 - $134,640 a year
- Full-time
- Microsoft Excel
- English
- Office
- Health insurance
- Dental insurance
8d
Manager, Media Production
Sysmex —Vernon Hills, IL
- $85,680 - $134,640 a year
- Full-time
- Microsoft Excel
- Bachelor's degree
- Travel
- Health insurance
- Dental insurance
7d
Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)
AbbVie —North Chicago, IL
- $109,500 - $208,500 a year
- Full-time
- Hybrid work
- Bachelor of Science
- 8 years
- Analysis skills
- Paid holidays
- Health insurance
Program Manager, Medical & Scientific Affairs (IVD, Medical Device)
Leica Biosystems —Deer Park, IL
- $130,000 - $145,000 a year
- Full-time
- Remote
- Medicine
- Bachelor's degree
- Continuous improvement
- Health insurance
- Dental insurance
7d
Project Manager
Quest Diagnostics —Wood Dale, IL
- $80,000 - $100,000 a year
- Full-time
- Writing skills
- HIPAA
- Mid-level
- Employee stock purchase plan
- Disability insurance
Quick Apply
4d
Clinical Trial Reimbursement (CTR) Senior Manager, HE&R
Abbott Laboratories —Abbott Park, IL
- $113,300 - $226,700 a year
- Full-time
- 5 years
- Senior level
- Associate's degree
- Health insurance
- Tuition reimbursement
Clinical Trial Lead
Prolaio —Chicago, IL
- From $115,000 a year
- Hybrid work
- Writing skills
- Presentation skills
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Quick Apply
9d
Biomarker Operations Manager
AbbVie —North Chicago, IL
- $65,500 - $125,500 a year
- Full-time
- Hybrid work
- Word processing
- English
- Master's degree
- Paid holidays
- Health insurance
Senior Program Manager, CMC Portfolio Management
AbbVie —North Chicago, IL
- $124,500 - $236,500 a year
- Full-time
- Hybrid work
- Doctoral degree
- Microsoft Office
- Master's degree
- Paid holidays
- Health insurance
Mobile Project Manager
Prevail Health, Inc —Chicago, IL
- Email
- Computer science
- Azure
- Computer Science
- Health insurance
- Dental insurance
Sr. Director, Clinical Affairs
Sysmex —Lincolnshire, IL
- $210,000 - $330,000 a year
- Full-time
- Microsoft Outlook
- Computer literacy
- English
- Health insurance
- Dental insurance

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R&D Manager, Clinical Research

Medline Industries -
Northfield, IL

Apply Now

Job Details

Full-time
$134,000 - $201,000 a year

Benefits

Health insurance
401(k)
Paid time off
Employee assistance program

Qualifications

Product development research management
Clinical research methods
Nursing
Staff supervision
Project development phase management
Team member evaluation
Clinical staff policy implementation
ISO standards
Performance feedback (performance evaluation method)
Quality improvement leadership
Research project design
Team development
Hiring
Collaboration with product development teams
Clinical research compliance
Bachelor's degree
Staff policy implementation
Team training
Industry trends
Project management experience in healthcare
Managing clinical research teams
Contingency planning
Data interpretation
Organizational skills
Leading team collaboration initiatives
Biomedical regulatory compliance
Bachelor's degree in nursing
Managing projects
Project resource management
Clinical quality assurance standards

Full Job Description

Job SummaryThis is a hybrid position that is based out of our corporate headquarters in Northfield, IL. Candidates must be local to the Chicagoland area or opened to relocation. Manage the Clinical Research function within corporate R&D, including personnel, project execution, and clinical evidence generation supporting Medline product development. This role oversees internal product evaluations, clinical studies, and customer-partnered quality improvement initiatives to ensure timely, compliant, and high-quality outcomes.Job DescriptionResponsibilities:<ul><li>Manage a team executing clinical research activities, including internal product evaluations, internal/external clinical studies, and customer quality improvement projects.</li><li>Plan and allocate resources to support clinical projects and evolving business priorities.</li></ul><ul><li>Collaborate with divisional personnel, quality, regulatory, commercial, and legal to define study strategies, timelines, and execution plans.</li></ul><ul><li>Oversee the design and execution of clinical studies and product evaluations to generate evidence in support of product development and post-market activities.</li><li>Partner with customers to drive quality improvement projects and leverage real-world data for product insights.</li><li>Identify issues and risks that might delay a project and make recommendations or develop contingency plans.</li><li>Ensure all team activities comply with applicable regulatory standards (e.g., GCP) and ensure internal governing procedures are maintained.</li><li>Monitor emerging clinical trends, technologies, and competitive products to inform innovation and strategy.</li></ul>Management responsibilities include: <ul><li>Day-to-day operations of a group of employees.</li><li>Budgetary responsibility for the team.</li><li>Interpret and execute policies for departments/projects.</li><li>Recommend and implement new policies or modifications to existing policies.</li><li>Provide general guidelines and parameters for staff functioning.</li><li>Hiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies.</li></ul>Qualifications:<ul><li>Bachelor’s degree in a scientific or clinical discipline (e.g. Life Sciences, Nursing).</li><li>A least 4 years of experience in clinical research, clinical affairs, or R&D within the medical device or healthcare industry.</li><li>Experience in the indirect management of team members, including assisting in the development, training and assignment of work/projects to other members of a team.</li><li>Experience assessing and initiating actions independently. Experience taking charge of a situation, team or project.</li><li>Experience processing all relevant details, understanding and prioritizing their importance and drawing clear and concise conclusions.</li><li>Experience using time management skills such as prioritizing/organizing and tracking details and meeting deadlines of multiple projects with varying completion dates.</li></ul>Preferred Qualifications:<ul><li>Experience supervising and leading cross-functional teams.</li><li>Experience controlling and coordinating concurrent projects, competing priorities, and critical deadlines.</li><li>Working knowledge of applicable regulations and standards, including:<ul><li>Good Clinical Practice (GCP)</li><li>FDA clinical requirements (IDE, 21 CFR) or global equivalents</li><li>ISO 14155 (clinical investigation of medical devices)</li><li>Familiarity with post-market clinical/real-world evidence activities</li></ul></li></ul>Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing worldwide organization.The anticipated salary range for this position:$134,000.00 - $201,000.00 AnnualThe actual salary will vary based on applicant’s location, education, experience, skills, and abilities. This role is bonus and/or incentive eligible. Medline will not pay less than the applicable minimum wage or salary threshold.Our benefit package includes health insurance, life and disability, 401(k) contributions, paid time off, etc., for employees working 30 or more hours per week on average. For roles where employees work less than 30 hours per week, benefits include 401(k) contributions, paid time off, as well as access to the Employee Assistance Program, Employee Resource Groups and the Employee Service Corp. For a more comprehensive list of our benefits please click <a target="_blank" href="https://urldefense.com/v3/__https:/digital.alight.com/medline__;!!DjNdo6avjEs!o-bxZ6fy_WNH13q2FLYYmUMb1U4cic3ioox3ulm5dkpyivWM09cd64RN8rHuDH5AQKNiwEzHU2VbVJht5ginULSy5aJGsA$">here</a>.We’re dedicated to creating a Medline where everyone feels they belong and can grow their career. We strive to do this by seeking diversity in all forms, acting inclusively, and ensuring that people have tools and resources to perform at their best. Explore our Belonging page <a target="_blank" href="https://www.medline.com/about-us/belonging/">here</a>.Medline Industries, LP is an equal opportunity employer. Medline evaluates qualified individuals without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, age, disability, neurodivergence, protected veteran status, marital or family status, caregiver responsibilities, genetic information, or any other characteristic protected by applicable federal, state, or local laws.

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Refine Your Search

clinical project manager jobs in deerfield, il

R&D Manager, Clinical Research

Clinical Project Manager

Senior Clinical Project Manager

Software Project Manager

Program Implementation Manager, Clinical Studies

Project Manager – Doula Program & Women’s Health

Epidemiology Study Operations Manager

Clinical Data Management Specialist

Senior Manager, Clinical Quality Assurance

Manager, Travel & Expense Program

Manager, Media Production

Manager, Clinical Data and Reporting Standards - SDTM Programming (Hybrid)

Program Manager, Medical & Scientific Affairs (IVD, Medical Device)

Project Manager

Clinical Trial Reimbursement (CTR) Senior Manager, HE&R

Clinical Trial Lead

Biomarker Operations Manager

Senior Program Manager, CMC Portfolio Management

Mobile Project Manager

Sr. Director, Clinical Affairs

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