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Live In Clinical Project Manager Jobs in Frederick, MD

PharmaOut

Clinical Project Manager

Gaithersburg, MD · On-site

This role will be key in developing internal Clinical Operations systems and procedures to improve ... Provides updates on project status and deliverables to Clinical Project Management leads ...

REGENXBIO

Sr Clinical Project Manager

Rockville, MD · On-site

The opportunity Senior Clinical Project Manager (Sr. CPM) is the primary operational contact for ... Responsible for and participates in clinical service provide (vendor) selection and development of ...

Corinth Consulting Group

Project Manager

Leesburg, VA · Hybrid

Corinth Consulting Group is seeking a dynamic and experienced Project Manager to join our team. As ... Candidates that live in a Federally designed HUBZone Area, per the official SBA HUBZone Map are ...

The Emmes Company, LLC

Sr. In-House CRA

Rockville, MD · On-site

Provides project teams with trial progress tracking by updating the Clinical Trial Management ... Assists in audit preparation activities as needed. * Assists the CRA in Issue and Action Item (AI ...

New

Emmes

Sr. In-House CRA

Rockville, MD · On-site +1

Provides project teams with trial progress tracking by updating the Clinical Trial Management ... Assists in audit preparation activities as needed. * Assists the CRA in Issue and Action Item (AI ...

Eichberg Construction

Be Seen First

Commercial Project Manager

Rockville, MD · On-site

$90K - $110K/yr

We are growing and need to add to our Project Management Team. If you have 5+ years' experience in ... and live in the DC area, we want to talk to you. We've been around 40+ years, have a great ...

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Live In Clinical Project Manager information

See Frederick, MD salary details

$28

$60

$107

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

As of Aug 22, 2026, the average hourly pay for live in clinical project manager in Frederick, MD is $60.35, according to ZipRecruiter salary data. Most workers in this role earn between $42.07 and $70.77 per hour, depending on experience, location, and employer.

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 cities near Frederick, MD are hiring for Live In Clinical Project Manager jobs?

Cities near Frederick, MD with the most Live In Clinical Project Manager job openings:

Live In Clinical Project Manager jobs near you

Clinical Project Manager

PharmaOut

Gaithersburg, MD • On-site

Full-time

Re-posted 5 days ago

Job description

Job Description This role will be key in developing internal Clinical Operations systems and procedures to improve all aspects of Clinical Study related business processes and will work very closely with the Associate Director of Clinical Operations along with the US Site Head. Location: Gaithersburg, Maryland Responsibilities: Participates in the planning, implementation and management of pre-IND through Phase I-II clinical trials, in collaboration with Contract Research Organization (CRO) partners, if applicable. Manage day to day activities of all aspects of clinical studies including study plans, timelines, problem identification and resolution, status reports and budget to ensure timely delivery of completed study reports to the project teams.

Contributes to development of RFPs and participates in selection of CROs/vendors. Manages CRO and vendor activities to ensure adherence to deliverables and timelines. Provides updates on project status and deliverables to Clinical Project Management leads (deliverables may include project status reports, vendor reports, trackers, meeting minutes/action items).

Contributes to development of study budget(s). Maintains primary responsibility for the content of and execution on all study-related operational plans, such as study operations manuals, vendor manuals, safety plans, project management plans, communication plans, and quality plans, whether developed internally or externally. Oversees investigator recruitment/selection and the conduct of trials at investigative sites.

Participate as necessary in monitoring visits (co-monitoring), reviews monitoring visit reports and ensures CRO quality within trials, if applicable. Plans, executes, and leads Investigators Meetings, if applicable. Contributes to development of internal Clinical Operations systems to improve business processes.

Develops relationships with Key Opinion Leaders as applicable for key I-Mab development programs. Prepare and present study or project specific updates. Represent Project Management & Clinical Operations in partnered development programs.

Mentors junior level Clinical Research Associates. Qualifications: Life sciences or medical background is required. 6+ years of industry experience (biotech/pharma) with at least 2-5 (will determine level) years of project management experience Experience in Phase 1 Oncology trials.

Strong understanding of ICH, GCP and relevant regulatory requirements The ability to work with cross-functional teams in a matrix environment is a must Strong organizational and time management skills; detailed oriented; excellent interpersonal and communication skills Proficiency with Microsoft Outlook, Excel, Word, PowerPoint and Project.

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