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Clinical Operations Jobs in Oregon (NOW HIRING)

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team. In this leadership role, you will be responsible for the management, development, and operational ...

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team. In this leadership role, you will be responsible for the management, development, and operational ...

Our platform expands clinical capacity, improves diagnostic quality by combining human expertise with AI, and turns operational complexity into strategic advantage through seamless integration or ...

This role bridges clinical and administrative functions, ensuring that the team operates ... Manage day-to-day clinic operations including scheduling, staffing, and workflow * Oversee client ...

Responsible for clinical quality and or administrative (operational) activities as assigned in Ambulatory Surgery Centers (ASC). This position requires a registered nurse with experience in quality ...

Responsible for clinical quality and or administrative (operational) activities as assigned in Ambulatory Surgery Centers (ASC). This position requires a registered nurse with experience in quality ...

OR · On-site

Partner closely with Global Program Heads, Clinical Operations, Regulatory Affairs, Medical Affairs, and the Therapeutic Business Unit Head to ensure clinical trial objectives are integrated into the ...

You will serve as a clinical science lead within cross-functional teams-partnering closely with Clinical Operations, Biostatistics, Medical Affairs, and Regulatory to drive study execution, identify ...

OR · On-site

Work closely with Clinical Operations, Medical Affairs, and asset matrix teams to ensure compliance with organizational SOPs * Assist in development and participate as needed, in Steering Committees ...

This role reports to the Clinical Operations Team in overseeing clinical work, supporting staff to follow appropriate policies and procedures, and in ensuring company culture and client experience is ...

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Clinical Operations information

See Oregon salary details

$37K

$103.7K

$197.2K

How much do clinical operations jobs pay per year?

As of Jul 15, 2026, the average yearly pay for clinical operations in Oregon is $103,655.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,700.00 and $120,000.00 per year, depending on experience, location, and employer.

How does a Clinical Operations professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Operations professionals play a central role in coordinating activities among various teams such as regulatory affairs, data management, biostatistics, and clinical research associates. They ensure that timelines are met, protocols are followed, and all departments are aligned with trial objectives. Regular meetings, clear communication, and the ability to anticipate and resolve operational challenges are essential to successful collaboration. This cross-functional teamwork helps maintain trial quality and regulatory compliance throughout the study.

What is clinical operations?

Clinical operations refers to the planning, management, and execution of clinical trials and research studies within the healthcare and pharmaceutical industries. Professionals in clinical operations ensure that studies are conducted efficiently, ethically, and in compliance with regulatory requirements. Their responsibilities may include site management, patient recruitment, data collection, and ensuring protocol adherence. The goal is to facilitate the safe and effective development of new medical treatments and therapies.

What is the difference between Clinical Operations vs Clinical Research Associate?

AspectClinical OperationsClinical Research Associate
Required CredentialsBachelor's degree, experience in clinical trial managementBachelor's degree, often with certification in clinical research
Work EnvironmentProject management, coordinating multiple trial sitesMonitoring clinical sites, ensuring protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, CROs, pharmaceutical companies
Common Search & ComparisonFocuses on trial oversight and managementFocuses on site monitoring and data verification

Clinical Operations professionals oversee the planning, coordination, and management of clinical trials, ensuring they run smoothly across multiple sites. Clinical Research Associates primarily monitor clinical trial sites, verify data accuracy, and ensure compliance with protocols. While both roles require knowledge of clinical research, Clinical Operations has a broader scope involving project management, whereas CRAs focus on site-level monitoring.

What are the key skills and qualifications needed to thrive in Clinical Operations, and why are they important?

To thrive in Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and electronic data capture (EDC) platforms is essential. Strong leadership, problem-solving, and communication skills help coordinate teams and ensure project timelines are met. These skills are crucial for guaranteeing efficient, compliant, and successful clinical trial execution in a highly regulated environment.
What are the most commonly searched types of Clinical Operations jobs in Oregon? The most popular types of Clinical Operations jobs in Oregon are:
What are popular job titles related to Clinical Operations jobs in Oregon? For Clinical Operations jobs in Oregon, the most frequently searched job titles are:
What cities in Oregon are hiring for Clinical Operations jobs? Cities in Oregon with the most Clinical Operations job openings:

Clinical Operations Manager

PSI CRO

On-site, Remote

Full-time

Posted 9 days ago


Job description

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

PSI is seeking an experienced and people-focused Clinical Operations Manager to join our team.

In this leadership role, you will be responsible for the management, development, and operational oversight of CRA staff. You will lead and mentor a high-performing team while ensuring efficient resource utilization, operational excellence, and the successful delivery of clinical trials. This position requires a collaborative leader who is passionate about developing people, driving quality, and partnering across functions to support study execution.

This is a home-based role based in the United States. 

The scope of responsibilities will include:

  • Line manage, coach, mentor, and develop Clinical Research Associates across multiple experience levels.
  • Manage hiring, onboarding, performance management, and professional development activities.
  • Oversee resource allocation, workload planning, and utilization across clinical trials.
  • Collaborate with Project Managers and cross-functional teams to ensure successful study delivery.
  • Monitor staff performance and support operational efficiency through established departmental metrics.
  • Implement departmental quality controls and contribute to the development and continuous improvement of quality systems and processes.
  • Prepare for and participate in internal audits, sponsor audits, and regulatory inspections.
  • Support trial execution by resolving operational challenges and facilitating communication between project teams and investigational sites.
  • Participate in feasibility assessments for new and ongoing studies.
  • Support business development activities, including client meetings, networking events, and operational discussions, as needed.
Qualifications
  • MD, PharmD, or a university degree in Life Sciences, or an equivalent combination of education, training, and experience.
  • Minimum of 5 years of clinical research industry experience, including demonstrated team management or people leadership experience.
  • Previous experience working independently as an onsite Clinical Research Associate (CRA) is required.
  • Previous experience managing or mentoring clinical research professionals in a CRO, sponsor, or related clinical research environment.
  • Strong leadership, coaching, and employee development skills.
  • Experience with resource planning, workload management, and performance management.
  • Working knowledge of ICH-GCP, applicable regulatory requirements, and clinical trial operations.
  • Experience supporting audits, inspections, and quality initiatives is preferred.
  • Excellent communication, organizational, and problem-solving skills.
  • Proficiency with Microsoft Office applications and clinical research systems.
  • Advanced English proficiency (written and spoken).
  • Strong interpersonal skills with the ability to build trust, foster collaboration, and develop high-performing teams.
Additional Information

All your information will be kept confidential according to EEO guidelines.