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Hourly Clinical Project Manager Jobs in Washington

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)

The opportunity Senior Clinical Project Manager (Sr. CPM) is the primary operational contact for the study, the lead for the cross-functional team in the execution of the study. This person will be ...

MedTech Site Manager 1

Washington, DC · On-site

$74K - $124K/yr

Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan. * Assist project manager with clinical study planning and ...

Ensure that monitoring activities (remote and on-site) are completed in accordance with company/client SOPs and Clinical Monitoring Plan. * Assist project manager with clinical study planning and ...

You will collaborate with clinical, administrative, and technical teams to help ensure projects ... Support senior project managers in the planning, scheduling, and execution of VA healthcare program ...

... based, clinically accurate, accessible, and culturally sensitive educational materials ... Project Management Professional (PMP) certification or equivalent project management certification.

... based, clinically accurate, accessible, and culturally sensitive educational materials ... Project Management Professional (PMP) certification or equivalent project management certification.

SUMMARY: The Project Manager is responsible for supporting the project team with the daily ... hourly) range for this position is $105,000.00 - $140,000.00 DAVIS is committed to providing our ...

SUMMARY: The Project Manager is responsible for supporting the project team with the daily ... hourly) range for this position is $105,000.00 - $140,000.00 DAVIS is committed to providing our ...

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Hourly Clinical Project Manager information

What is the difference between Hourly Clinical Project Manager vs Clinical Research Coordinator?

AspectHourly Clinical Project ManagerClinical Research Coordinator
CredentialsBachelor's degree, relevant certifications (e.g., CCRP)Bachelor's degree, often in health or science fields
Work EnvironmentManages multiple projects, oversees teams, works in clinical settingsSupports clinical trials, interacts directly with participants and staff
Employer & Industry UsagePharmaceuticals, biotech, contract research organizationsHospitals, clinics, research institutions

The Hourly Clinical Project Manager typically oversees multiple clinical trials, managing teams and project timelines, while the Clinical Research Coordinator focuses on day-to-day trial operations and participant coordination. Both roles require relevant certifications and work within the clinical research industry, but their responsibilities and scope differ significantly.

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

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For Hourly Clinical Project Manager jobs in Washington, the most frequently searched job titles are:

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Cities in Washington with the most Hourly Clinical Project Manager job openings:

Clinical Project Manager

PharmaOut

Gaithersburg, MD • On-site

Full-time

Re-posted 6 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.