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Clinical Project Management Jobs in Washington (NOW HIRING)

IQVIA

Project Management Analyst

Columbia, MD · On-site +1

$49K - $124K/yr

We are seeking Project Management Analyst to join IQVIA Laboratories at Columbia, MD. We hire ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

IQVIA, Inc.

Project Management Analyst

Columbia, MD · On-site

$49K - $124K/yr

We are seeking Project Management Analyst to join IQVIA Laboratories at Columbia, MD. We hire ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

IQVIA

Project Management Analyst

Columbia, MD · On-site +1

$49K - $124K/yr

We are seeking Project Management Analyst to join IQVIA Laboratories at Columbia, MD. We hire ... IQVIA is a leading global provider of clinical research services, commercial insights and health ...

Peraton

Technical Project Management

Arlington, VA · On-site

$104K - $166K/yr

Coast Guard and participating community care providers, allowing clinicians to easily access a Veteran's full medical history in one location. The Technical Project Manager will be tasked with ...

Peraton

Technical Project Management

Arlington, VA · On-site

$104K - $166K/yr

Coast Guard and participating community care providers, allowing clinicians to easily access a Veteran's full medical history in one location. The Technical Project Manager will be tasked with ...

Peraton

Technical Project Management

Arlington, VA · On-site

$104K - $166K/yr

Coast Guard and participating community care providers, allowing clinicians to easily access a Veteran's full medical history in one location. The Technical Project Manager will be tasked with ...

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All JobsClinical Project Management JobsClinical Project Management Jobs in Washington

Clinical Project Management information

See Washington salary details

$32

$68

$122

How much do clinical project management jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for clinical project management in Washington is $68.75, according to ZipRecruiter salary data. Most workers in this role earn between $47.93 and $80.58 per hour, depending on experience, location, and employer.

What is clinical project management?

Clinical project management involves planning, coordinating, and overseeing clinical trials or research projects to ensure they are completed on time, within budget, and according to regulatory requirements. Clinical project managers are responsible for managing cross-functional teams, timelines, budgets, and resources, as well as communicating with stakeholders and ensuring compliance with Good Clinical Practice (GCP) guidelines. Their work is essential to the successful execution of clinical studies and the advancement of new medical treatments.

What are some of the common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing timelines with various stakeholders, and handling regulatory documentation for different regions. Communication is key, as PMs must keep both internal teams and external partners aligned despite geographic and cultural differences. Effective risk management and proactive problem-solving skills are essential to keep studies on track and maintain data quality.

What are the key skills and qualifications needed to thrive as a clinical project manager, and why are they important?

To thrive as a Clinical Project Manager, you need a strong background in clinical research, project management, and regulatory compliance, often supported by a life sciences degree and relevant industry experience. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and project management certifications like PMP are highly valued. Outstanding organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These competencies ensure clinical trials are conducted efficiently, compliantly, and within budget, ultimately supporting successful study outcomes.

What is the difference between Clinical Project Management vs Clinical Research Associate?

AspectClinical Project ManagementClinical Research Associate
CredentialsTypically requires a degree in life sciences, project management certification (e.g., PMP)Usually holds a degree in life sciences or healthcare; certifications like CCRA are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates across departmentsMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageUsed by pharmaceutical, biotech companies, and CROs for overseeing projectsEmployed by sponsors, CROs, and sites to ensure trial quality and compliance

Clinical Project Managers focus on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. Clinical Research Associates primarily monitor clinical sites and ensure compliance with protocols. Both roles are essential in the clinical research process but differ in scope and responsibilities.

What are popular job titles related to Clinical Project Management jobs in Washington?

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

What job categories do people searching Clinical Project Management jobs in Washington look for?

The top searched job categories for Clinical Project Management jobs in Washington are:

What cities in Washington are hiring for Clinical Project Management jobs?

Cities in Washington with the most Clinical Project Management job openings:

Clinical Project Management jobs near you
Infographic showing various Clinical Project Management job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $143,003 per year, or $68.8 per hour.

Clinical Project Manager

PharmaOut

Gaithersburg, MD

Full-time

Re-posted 10 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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