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Live In Clinical Project Manager Jobs in Kansas (NOW HIRING)

Epic

Project Manager

Lawrence, KS · On-site

... are providers go live with our software. • Enjoy autonomy in decision-making with our full support and guidance. • Manage projects at the most innovative health systems on the planet.

Epic

Project Manager

Topeka, KS · On-site

... are providers go live with our software. • Enjoy autonomy in decision-making with our full support and guidance. • Manage projects at the most innovative health systems on the planet.

Epic

Project Manager

Overland Park, KS · On-site

... are providers go live with our software. • Enjoy autonomy in decision-making with our full support and guidance. • Manage projects at the most innovative health systems on the planet.

LUX Infusion

Project Manager

Overland Park, KS · On-site

$100K - $110K/yr

See your work in a new light. At LUX Infusion, we're reimagining infusion care to be more human ... As a clinician-led, U.S.-based organization, we put people first - helping patients feel seen and ...

Integrated Resources INC

Project Manager

Topeka, KS

We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Title: Project Manager Job Location: Topeka, Kansas Job ...

Nexus 5 Group

Project Manager Multifamily

Merriam, KS

$108K - $133K/yr

Project Management * Oversee multiple projects in various stages including budgeting ... Capacity to live and work within the Nexus 5 Core Values (Integrity, Commitment, Customer ...

Nexus 5 Group

Project Manager Multifamily

Merriam, KS · On-site

$108K - $133K/yr

Project Management * Oversee multiple projects in various stages including budgeting ... Capacity to live and work within the Nexus 5 Core Values (Integrity, Commitment, Customer ...

GBA Companies

Project Manager

Lenexa, KS · On-site

The Project Manager plays a key role in supporting the GBAFS Senior Project Manager in achieving annual goals. Additionally, the Project Manager is responsible for overseeing assigned projects while ...

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Live In Clinical Project Manager information

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 are the most commonly searched types of Clinical Project Manager jobs in Kansas? The most popular types of Clinical Project Manager jobs in Kansas are:
Live In Clinical Project Manager jobs near you
Sr. Clinical Project Manager, IQVIA Biotech

Sr. Clinical Project Manager, IQVIA Biotech

IQVIA

Overland Park, KS • On-site

$93K - $232K/yr

Full-time

Posted 8 days ago

IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

45th of 204 rated it services

Job description

IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Overview
The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.

Key Responsibilities

  • Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards.
  • Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training.
  • Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables.
  • Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones.
  • Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable.
  • Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans.
  • Collaborate with internal functional groups to support study execution and overcome operational challenges.
  • Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders.
  • Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery.
  • Manage scope changes and oversee change control processes in collaboration with stakeholders.
  • Promote continuous improvement by sharing lessons learned and best practices.
  • Mentor and support the development of junior team members and contribute feedback on team performance.

Qualifications

  • Bachelor's Degree in Life Sciences or a related field required; advanced degree preferred.
  • Requires greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience.
  • Proven ability to manage complex, global clinical trials and cross-functional teams.
  • Strong leadership, communication, and stakeholder management skills.
  • Demonstrated ability to manage budgets, timelines, and risk proactively.
  • Experience leading bid defenses and client engagements is preferred.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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