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

$80 - $100/hr

Senior Clinical Trial Project Manager MD (m,f,d) 80-100% In this client‑facing consulting role, as part of the clinical team you will take full responsibility for the setup and operational ...

Senior Helpers of Dayton is urgently seeking a Live-In Caregiver to provide high-quality, around ... that management trusts people to do a good job without watching over their shoulders. About the ...

Senior Helpers of Dayton is urgently seeking a Live-In Caregiver to provide high-quality, around ... that management trusts people to do a good job without watching over their shoulders. About the ...

Senior Helpers of Dayton is urgently seeking a Live-In Caregiver to provide high-quality, around ... that management trusts people to do a good job without watching over their shoulders. About the ...

Overview TheKey is currently hiring LIVE IN caregivers to support clients in Columbus. Earn TOP PAY ... Referral Bonuses * 24/7 Caregiver Support & local management * Career development opportunities ...

$91.18 - $125.37/hr

Projektleiter / Project Manager Clinical Trials Vollzeit Festanstellung Deine Mission bei uns ... In dieser Rolle hältst Du die Projektfäden Deiner klinischen Studie zusammen, steuerst Abläufe ...

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Live In Clinical Project Manager information

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 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 are the most commonly searched types of Clinical Project Manager jobs in Ohio?

The most popular types of Clinical Project Manager jobs in Ohio are:

Senior Clinical Trial Project Manager MD (m,f,d) 80-100%

regenold GmbH

On-site

$80 - $100/hr

Other

Retirement

Posted 5 days ago


Job description

Senior Clinical Trial Project Manager MD (m,f,d) 80-100%

In this client‑facing consulting role, as part of the clinical team you will take full responsibility for the setup and operational management of clinical investigations on behalf of our clients in the medical device and IVD sectors.

At regenold, we work in a client-focused environment that is dynamic and responsibility-driven.

If you are someone who enjoys taking ownership, guiding and advising clients with confidence and managing projects independently, this role is for you.

If you prefer purely procedural or methodical work, this role may not be for you…

Your main tasks will include:
  • Taking responsibility for the setup and operational delivery of clinical investigations for regenold clients in the medical device and IVD field
  • Selecting, qualifying, and overseeing CROs and other external vendors, including feasibility, budget negotiations, contracting and performance management
  • Sponsor oversight activities to ensure study quality, compliance and timely execution
  • Preparing and submitting Clinical Trial Applications and managing requests and deficiency communications
  • Driving cross-functional stakeholder communication and ensuring effective study governance structures
  • Managing clinical investigations end to end, from study planning to close‑out
  • Reviewing key study documentation, including CRO monitoring outputs and deviations, ensuring documentation quality throughout the project
Your education, skills, knowledge and experience
  • CRA background preferred
  • 6+ years of hands‑on experience in managing clinical trials with solid experience in clinical investigations.
  • IVD experience is beneficial but not essential
  • Proven track record in senior roles such as (Senior) Clinical Project Manager / Lead, ideally across different settings such as Pharma and CRO
  • Strong experience in sponsor oversight and vendor management
  • Thorough knowledge of GCP and the clinical regulatory environment
  • Excellent written and verbal communication skills in German and English
  • Strong organizational skills, with the ability to prioritize, multitask, communicate effectively and deliver under pressure
  • Degree in Life Sciences or equivalent
what we offer
  • International diversity - in the team and in the projects
  • Long‑term prospects - for professional and personal development, we offer a wide range of tasks and individually tailored training opportunities right from the onboarding phase
  • Flexibility, freedom and personal responsibility - through flat hierarchies, short decision‑making processes and family‑friendly working time models, with something for everyone …
  • One of the most beautiful regions in Germany, also called the Toscana of Germany, on the edge of the Black Forest in the border triangle of Germany/ France/ Switzerland
  • Attractive salary, company pension scheme, capital‑forming benefits, JobRad, Hansefit, Shuttle Transfer Freiburg-Badenweiler and much more, promised …
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