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Live In Clinical Project Manager Jobs (NOW HIRING)

PSI CRO

Regional Project Lead

The Regional Project Lead is a senior level clinical trial manager who oversees, manages, and coordinates activities of project teams in designated countries and ensures consistency of Clinical ...

Syneoshealth

OR

Senior Clinical Project Manager - Inflammation/ Phase 2b (Sponsor Dedicated - Remote; Preference ... Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you ...

IQVIA

Senior Clinical Project Manager, CNS

Durham, NC

$93K - $232K/yr

We are seeking a US-based Senior Project Manager with proven experience in Central Nervous System (CNS) clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management ...

Regal Medical Group, Inc.

$104K/yr

Lead and manage projects related to clinical care management and systems. * Triage urgent issues ... Participates in on-site and off-site meetings/events as part of building and maintaining normal ...

SYNERGY HomeCare

Live-In Caregiver

Matawan, NJ

**Live-In Caregiver****Join the Synergy Effect at SYNERGY HomeCare of Woodbridge**At SYNERGY HomeCare ... activities, medication management, and personal care* Building trust and forming strong ...

Right at Home

Live-In's

Skokie, IL · 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 ...

PSI CRO

Senior Project Manager

At least 7 years of industry experience in clinical research * At least 4 years of global, project-level clinical project management experience, including management of all project phases from ...

AHEAD

Live-In Caregiver

Levittown, PA · On-site

$235/day

Seeking Non-Medical/Non-Skilled Live-In Caregivers As a Non-Medical Home Healthcare Live-In, your ... Medication Management: Ensure that clients take their prescribed medications on time. You will ...

Southern Companions

Live-In Caregiver

Athens, GA

$200/day

Reliable - time management is a must. * Valid TB test * In person CPR/First Aid Certification ... Starting $200/day live-in * Paid weekly We believe in recognizing hard work and dedication and ...

Senior Helpers - Bolingbrook, IL

IL · On-site

$220/day

NOW HIRING -- LIVE-IN CAREGIVERS We're growing our team and hiring multiple Live-In Caregivers to ... Employee-Centric Management: We prioritize your well-being and create a safe, inclusive, and ...

Southern Companions

Live-In Caregiver

Gainesville, GA · On-site

$200/day

Reliable - time management is a must. * Valid TB test * In person CPR/First Aid Certification ... Starting $200/day live-in * Paid weekly We believe in recognizing hard work and dedication and ...

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Live In Clinical Project Manager information

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

As of Jun 20, 2026, the average hourly pay for live in clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 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 are hiring for Live In Clinical Project Manager jobs? Cities with the most Live In Clinical Project Manager job openings:
What are the most commonly searched types of Clinical Project Manager jobs? The most popular types of Clinical Project Manager jobs are:
What states have the most Live In Clinical Project Manager jobs? States with the most job openings for Live In Clinical Project Manager jobs include:
Live In Clinical Project Manager jobs near you

Regional Project Lead

PSI CRO

Remote

Full-time

Posted 11 hours ago

Job description

Company Description
We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them.
If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.
Job Description
The Regional Project Lead is a senior level clinical trial manager who oversees, manages, and coordinates activities of project teams in designated countries and ensures consistency of Clinical Operations processes across regions. They ensure meeting study milestones are met by the project team on a country and regional level.
  • Ensures planning, implementation, and management of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g., PSI QSDs or Sponsor QMS documents)
  • Acts as primary or secondary project management contact for the project team and PSI support services in designated countries
  • Performs study status review and progress reporting (if delegated by the Project Manager)
  • Collects and reports project status updates for designated regions, both internally and externally
  • Develops and updates project planning documents, essential study documents and project manuals/ instructions
  • Manages and reports on Key Performance Indicators (KPIs) for designated countries and clinical project team members
  • Ensures that the project timelines and subject enrollment targets are met in designated countries
  • Coordinates maintenance of study-specific and corporate tracking systems
  • Coordinates site contractual startup and budget negotiations
  • Establishes communication lines within the project team and supervises clinical project team members' performance
  • Identifies, escalates and resolves resourcing and performance issues
  • Conducts and supervises therapeutic area training of the project team (if delegated by the Project Manager)
  • Prepares presentations and conducts training of Investigators
  • Ensures team compliance with project-specific training matrix
  • Performs field training of Monitors tailored to the project needs
  • Supervises preparation, conduct and reporting of site selection, site initiation, routine monitoring and closeout visits
  • Oversees investigator and site payments, as well as CRF data retrieval/ upload and monitoring and the query resolution process
  • Supervises project team preparation for study audits/ inspections and resolution of audit/ inspection findings
  • Coordinates conduct of supervised monitoring visits
  • Reviews site visit reports and ensures monitoring and reporting standards are met
  • Coordinates preparation of initial and follow-up Regulatory and Ethics Committee submissions and notifications
  • Oversees the safety information flow and participates in feasibility research
  • Reviews/approves project related expenses and timesheets (if delegated by the Project Manager)

Qualifications
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience is required
  • Prior experience in Clinical Research and on-site monitoring is required
  • Experience as a Study Manager/Clinical Trial Manager with the ability to supervise project activities as a Regional Lead or equivalent is required
  • Experience in Oncology is required
  • Experience in GI is preferred
  • Full working proficiency in English
  • Proficiency in MS Office applications, including MS Project
  • Communication, presentation and customer-service skills
  • Ability to negotiate and build relationships at all levels
  • Team building, leadership and organizational skills

For this position PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.
Additional Information
Advance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study.
For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

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