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Clinical Study Manager Jobs in Oregon (NOW HIRING)

Manage study contracting, budget and payment process for all clinical trial vendors including investigational sites. * Partner with department head to develop department procedures and develop ...

Position Summary This Study Abroad Manager position takes the lead role with the development and execution of a suite of 30+ OSU faculty-led programs across the university, and oversees the OSU GO ...

Clinical study design and execution : Oversee the development of clinical study plans from concept ... Leadership and project management : Demonstrated success in leading cross-functional teams and ...

Director, Clinical Science

OR · On-site +1

$79K - $108K/yr

Flexibility to engage with clinical collaborators and study teams across international, global time zones * Ability to engage in work-related international and domestic travel up to 25% to manage ...

Develop study-related documents with minimal Clinical Trial Manager guidance including: protocol, informed consent forms, training materials, protocol amendments, monitoring plans, synopses, and ...

OR · On-site

... managing the clinical scientists embedded within the biobanking workstream. PRIMARY RESPONSIBILITIES: Trial Strategy and Protocol Architecture * Design robust clinical study concepts, specifying ...

Central Study Coordinator I

OR · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Central Study Coordinator (CSC) position combines clinical research and project management skillsinto a singular role that delivers a strong customer experience for both patients and sites. Often ...

Clinical Scientist, Clinical Development

OR · On-site +1

$215K - $230K/yr

  • Medical

  • Retirement

  • PTO

Lead/Contribute to study design and amendments in collaboration with internal and external ... Collaborate with clinical operations, data management and CRO to develop and implement the overall ...

Clinical Trial Manager - Full Service

OR · On-site +1

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Reviews the study scope of work, budget and protocol content and ensures the clinical project team ... Data Management Plan, Communication Plan) as they relate to the clinical trial management ...

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Showing results 1-20

Clinical Study Manager information

See Oregon salary details

$30

$66

$101

How much do clinical study manager jobs pay per hour?

As of Aug 18, 2026, the average hourly pay for clinical study manager in Oregon is $66.10, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $74.47 per hour, depending on experience, location, and employer.

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

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are the most commonly searched types of Clinical Study jobs in Oregon?

The most popular types of Clinical Study jobs in Oregon are:

What are popular job titles related to Clinical Study Manager jobs in Oregon?

For Clinical Study Manager jobs in Oregon, the most frequently searched job titles are:

What cities in Oregon are hiring for Clinical Study Manager jobs?

Cities in Oregon with the most Clinical Study Manager job openings:

Infographic showing various Clinical Study Manager job openings in Oregon as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $137,483 per year, or $66.1 per hour.

Senior Manager, Clinical Trials

Natera

OR • On-site, Remote

Full-time

Posted 11 days ago


Natera rating

7.7

Company rating: 7.7 out of 10

Based on 38 frontline employees who took The Breakroom Quiz

56th of 120 rated laboratories


Job description

POSITION SUMMARY:

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests. This role manages clinical operations staff and all aspects of the trials independently, including study design, protocol implementation, site monitoring, and recruitment site management.

PRIMARY RESPONSIBILITIES:

  • Responsible for the implementation of clinical trial activities per study protocol. Works closely with investigative site personnel, CROs, and other study vendors

  • Manage and coach clinical research staff.

  • Manage study contracting, budget and payment process for all clinical trial vendors including investigational sites.

  • Partner with department head to develop department procedures and develop infrastructure.

  • Design study related documents, including but not limited to study protocol, informed consent forms, CRFs, and regulatory binders.

  • Train CROs, vendors, investigators and study coordinators on study protocol and relevant

  • Monitor and track clinical trial progress and provide status update to stakeholders.

  • Partner with other research and development groups to achieve deliverables.

  • This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job

  • Employee must complete training relating to HIPAA/PHI privacy, General Policies and Procedure Compliance training and security training as soon as possible but not later than the first 30 days of hire.

  • Must maintain a current status on Natera training requirements.

QUALIFICATIONS:

  • Bachelor's degree in life sciences, other relevant discipline, or equivalent required. Advanced degree preferred.

  • 5-10 years of clinical research experience, including at least 3-5 years of experience in managing clinical trials as a leading role.

  • 2+ years of experience of managing staff. Experience in managing CROs is preferred.

  • Experience managing all aspects of the trials independently, including study design, protocol implementation, site monitoring, sample management, and recruitment site management.

KNOWLEDGE, SKILLS, AND ABILITIES:

  • Familiar with the clinical research regulations.

  • Ability to collaborate with the study team, cross functional team members and external

  • Proficiency in MS Word, Excel and PowerPoint.

  • Good organization and planning skills.

  • Strong interpersonal skills and communication skills (both written and oral).

  • Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment.


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