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Live In Clinical Project Manager Jobs in Deerfield, IL

Work in an office (Wilmette, IL north of Chicago) with a dynamic, talented team Qualifications ... Clinical Project or Trial Manager * 7+ years' experience managing clinical trials including study ...

Established in 1991, Collabera is one of the fastest growing end-to-end information technology ... Appropriately advises management of project risks and presents recommendations for resolution.

Live-In's

Skokie, IL ยท On-site

$180 - $200/day

Want to join a company that truly makes a difference in the world? During these trying times, Right ... will be made by the management of this franchisee. All inquiries about employment at this ...

Live In Caregiver

Libertyville, IL ยท On-site

$600 - $850/wk

Paid time off Live-In Caregiver: A Calling, Not Just a Job At ComForCare , we are looking for ... Home Management: Handling light household needs. * Connection: Providing socialization and ...

We are seeking a compassionate and dedicated Live-In Caregiver to provide exceptional in-home care for individuals requiring support with daily activities and health management. This vital role ...

Live In Caregiver

Skokie, IL ยท On-site

$16.50 - $18/hr

... management techniques when necessary. Skills:- Experience in assisted living or senior care ... Currently seeking all positions, Full-time, Part-time, Live-In and Weekends. What you will be doing:

LIVE IN CAREGIVER

Skokie, IL ยท On-site

$16.50 - $18/hr

... management techniques when necessary. Skills:- Experience in assisted living or senior care ... Currently seeking all positions, Full-time, Part-time, Live-In and Weekends. What you will be doing:

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Live In Clinical Project Manager information

See Deerfield, IL salary details

$29

$61

$110

How much do live in clinical project manager jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for live in clinical project manager in Deerfield, IL is $61.73, according to ZipRecruiter salary data. Most workers in this role earn between $43.03 and $72.36 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a live in clinical project manager, and why are they important?

To thrive as a Live In Clinical Project Manager, you need strong project management skills, clinical research experience, and a relevant degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and certifications like PMP or GCP are typically essential. Exceptional organizational, leadership, and communication skills help you coordinate teams and maintain effective stakeholder relationships. These skills ensure that clinical projects are executed efficiently, ethically, and within regulatory standards, ultimately safeguarding patient safety and study integrity.

What is the difference between Live In Clinical Project Manager vs Clinical Project Coordinator?

AspectLive In Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree in life sciences or related field; often PMP or similar certificationsBachelor's degree in health sciences or related field; certification is a plus
Work EnvironmentLeads clinical trials, manages teams, and oversees project progress on-site or remotelySupports project activities, coordinates schedules, and assists managers
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical research sites

The Live In Clinical Project Manager typically holds more responsibilities, including leading clinical trials and managing teams, often requiring certifications like PMP. The Clinical Project Coordinator focuses on supporting project tasks and coordination. Both roles are essential in clinical research but differ in scope and seniority.

What is a live in clinical project manager?

A Live In Clinical Project Manager is a professional responsible for overseeing and coordinating clinical trials or healthcare projects, often in a residential or on-site setting. Their duties typically involve managing study protocols, ensuring regulatory compliance, coordinating with medical staff, and monitoring patient safety and data quality. They may be required to live on-site or near the project location to provide around-the-clock support and leadership. This role is crucial for the smooth operation and success of clinical programs, especially those requiring continuous oversight.

How does a live in clinical project manager typically collaborate with clinical staff and external stakeholders during a clinical trial?

A Live In Clinical Project Manager works closely with on-site clinical staff, including nurses, physicians, and research coordinators, to ensure that trial protocols are followed accurately and patient safety is prioritized. They also act as the primary point of contact between the site and external stakeholders such as sponsors, regulatory bodies, and vendor partners. Regular meetings, detailed reporting, and transparent communication are key aspects of the collaboration, helping to address challenges quickly and keep the project on track. This role requires strong interpersonal skills and the ability to adapt to dynamic clinical environments.
What cities near Deerfield, IL are hiring for Live In Clinical Project Manager jobs? Cities near Deerfield, IL with the most Live In Clinical Project Manager job openings:

Senior Clinical Project Manager

CEDENT

Chicago, IL โ€ข On-site

Full-time

Re-posted 19 days ago


Job description

Responsibilities

  • Contribute to our cutting-edge radiopharmaceutical development program
  • Conceptualize, plan, design, place, execute, and summarize clinical trials
  • Drive daily vendor and site management, including collaboration with Study Medical Monitor and KOLs to determine the medical and scientific needs
  • Effectively communicate project-related information including the planning and execution of meetings and presentations as well as creation and maintenance of metrics, e.g., dashboards, timelines, resources, and budgets
  • Contribute to regulatory filings (e.g., IND / IMPD / CTN, NDA)
  • Identify issues and propose solutions. Proactively assess potential risks to the clinical study and propose mitigation plans
  • Work in an office (Wilmette, IL north of Chicago) with a dynamic, talented team

Qualifications

MINIMUM EXPERIENCE

  • Biotech or Pharma company clinical operations experience in progressively responsible positions, including Senior/Clinical Project or Trial Manager
  • 7+ yearsโ€™ experience managing clinical trials including study design and initiation, oversight, study closeout, project management, and regulatory filings
  • Demonstrated ability to plan and execute Pharma-Sponsored clinical trials, managing vendors and resources in effective & creative manners to achieve business needs including on-time, on-budget, and on-spec study results for successful use in regulatory marketing applications
  • Thorough knowledge of ICH-GCP, Food and Drug Administration (FDA), and European regulations
  • Excellent communication (oral and/or written), leadership, and risk mitigation skills plus a positive attitude
  • Require minimal guidance; is able to function in an independent manner
  • Proven ability to effectively manage internal and external personnel in clinical trial conduct

PREFERRED EXPERIENCE

  • 9 yearsโ€™ clinical trials experience in pharmaceutical or biotechnology firms
  • Experience in oncology trials
  • Experience managing clinical trials in Europe and/or Australia
  • Experience in a small or growth-stage biopharma company

Cedent logo

About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008