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Clinical Research Program Manager Jobs in Spokane, WA

Surgery Partners

RESEARCH ANALYST

Post Falls, ID · On-site

As a specialized research professional, you would coordinate and manage clinical trials and help maintain the success of our clinical research department. The Research Analyst role directly ...

Cambia Health Solutions

Pharmacy Program Manager

Spokane, WA · On-site

$65.75 - $77.25/hr

Performs project management, team leadership, system analysis, research & design for purposes of project completion. Guides and assists in pharmacy clinical program outreach, maintains policy ...

Surgery Partners

RESEARCH ANALYST

Post Falls, ID · On-site

As a specialized research professional, you would coordinate and manage clinical trials and help maintain the success of our clinical research department. The Research Analyst role directly ...

Cambia Health Solutions

Pharmacy Program Manager

Spokane, WA · On-site

$65.75 - $77.25/hr

Performs project management, team leadership, system analysis, research & design for purposes of project completion. Guides and assists in pharmacy clinical program outreach, maintains policy ...

Uw

Research Operations Administrator

Spokane, WA · On-site

This role requires a sophisticated operational skill set encompassing program administration, research compliance, financial management, personnel coordination, and cross-institutional partnership ...

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Spokane, WA

Clinical Research Program Manager information

See Spokane, WA salary details

$45K

$93.6K

$151.2K

How much do clinical research program manager jobs pay per year?

As of Aug 10, 2026, the average yearly pay for clinical research program manager in Spokane, WA is $93,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,300.00 and $106,200.00 per year, depending on experience, location, and employer.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.
What are popular job titles related to Clinical Research Program Manager jobs in Spokane, WA? For Clinical Research Program Manager jobs in Spokane, WA, the most frequently searched job titles are:
What job categories do people searching Clinical Research Program Manager jobs in Spokane, WA look for? The top searched job categories for Clinical Research Program Manager jobs in Spokane, WA are:
What cities near Spokane, WA are hiring for Clinical Research Program Manager jobs? Cities near Spokane, WA with the most Clinical Research Program Manager job openings:
Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Spokane, WA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 1% Temporary, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $93,633 per year, or $45 per hour.

RESEARCH ANALYST

Northwest Specialty Hospital

Post Falls, ID • On-site

Full-time

Medical, Dental, Vision, Retirement

Posted 27 days ago

Job description

Northwest Specialty Hospital is seeking a Research Analyst to join our growing research team!
This is an on-sight, full-time position!
As a specialized research professional, you would coordinate and manage clinical trials and help maintain the success of our clinical research department. The Research Analyst role directly contributes to discovering new treatments for diseases, as well as ways to detect and diagnose disease and reduce the chances of patients developing progressive disease.
  • High level daily functions of the position include:
  • Review clinical protocols (study procedures/assessments and timelines); maintain working knowledge of all assigned protocols and amendments
  • Review patient electronic medical record and evaluate potential participants for eligibility as related to protocol inclusion/exclusion criteria
  • Conduct the informed consent process and discussions with research participants, including answering questions related to the study
  • Schedule appointments per study specific visit windows, conduct patient visits, and collect data in adherence with the assigned study protocol (including concomitant medications, medical history, pain assessment scales), assure all assessments are completed for each study visit per protocol
  • Maintain accurate records/source documents and transcribe source documents to electronic data capture system(s)
  • Identify and document adverse events, serious adverse events, protocol deviations
  • Prepare for monitoring visits, respond to sponsor queries, and complete all action items noted in monitoring follow-up letters

The Research Analyst will assist the Research Manager with duties pertaining to clinical research trials, assist in reviewing clinical research protocols (e.g., study procedures and timelines, inclusion and exclusion criteria, etc.), and assist in collection, and submission, of essential documents needed to initiate and maintain the study. This position will also screen potential research participants for eligibility using protocol specific inclusion and exclusion criteria; conduct, or participate in, the informed consent process with research participants; assure current, and amended, consent forms are appropriately implemented and signed; and conduct study-specific visits with participants. It will be important in this role to assure accurate data collection, case report form completion, and electronic data capture entries. This position will also maintain study timelines, collect data as required by the protocol, and maintain study files in accordance with FDA regulations, ICH-GCP guidelines, and sponsor requirements.
Qualifications and Preferred Experience:
  • High School Diploma
  • Excellent interpersonal skills to work effectively with clinicians, patients, administrators, monitors and sponsors
  • Familiarity with Microsoft Office Suite and electronic data capture
  • Knowledge of medical terminology
  • Have, or acquire, high-level knowledge of Regulatory Affairs (FDA medical device regulations and ICH-Good Clinical Practice guidelines)
  • Candidate should be seeking long-term employment opportunity
  • Science oriented with excellent organizational skills to independently manage workflow
  • Medical training a plus (LPN, MA); will train strong candidate in research-specific responsibilities

About Northwest Specialty Hospital:
Northwest Specialty Hospital is widely known for being a center of excellence and is proudly owned and operated by local physicians. The physicians have invested personally, professionally and financially in the care of the patients and the staff. They have dedicated their lives to creating a hospital that allows them to practice on their own terms and do what's best for patients. Northwest Specialty Hospital includes 12 operating rooms and 28 inpatient beds, along with a variety of clinics and services throughout Kootenai County, that span across multiple specialties.
Northwest Specialty Hospital has earned numerous awards for patient care, surgical skill, medical care, and employee satisfaction. Northwest Specialty Hospital has been recognized as one of the Best Places to Work in the Inland Northwest for five consecutive years!! Companies throughout Washington and Idaho were selected based on employee feedback about benefits, work environment, job satisfaction, and other factors. We continue to receive this distinguished honor based on our great company culture, patient focused approach, and robust benefits package!
Some of our amazing perks and benefits offered to employees are:
  • Company-sponsored events such as Silverwood Days, sporting events, BBQs and holiday parties
  • Comprehensive health care coverage with options for Medical, Dental, & Vision Insurance
  • Tuition reimbursement
  • Growth opportunities, ongoing education, training, leadership courses
  • A generous 401K retirement plan
  • A variety of discounts throughout the hospital and community are available to employees
  • Wellness benefits offered to staff such as: weight loss challenge, access to a dietitian, and discount gym memberships
  • Culture that promotes and supports work/life balance

**Northwest Specialty Hospital is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.**
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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