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Clinical Study Manager Jobs in Oregon (NOW HIRING)

Natera

OR · On-site

Manage study contracting, budget and payment process for all clinical trial vendors including investigational sites. * Design study related documents, including but not limited to study protocol ...

Arcus Biosciences

Senior Clinical Program Manager

$175K - $190K/yr

Summary The Senior Clinical Program Manager (Sr. CPM) is responsible for the strategic and ... Oversee day-to-day study management activities from start-up through close-out. * Anticipate ...

Pulse Biosciences

OR · On-site

S/he is responsible for completion of all study deliverables, ensuring the highest level of data ... Proficient in clinical trial management systems including electronic data capture (EDC) software ...

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

Manage study timelines, deliverables, risks, and issue resolution * Oversee external vendors, CROs, central laboratories, imaging vendors, and specialty providers * Coordinate Clinical Trial Team ...

Arcus Biosciences

$175K - $190K/yr

This role will work on cross-functional study management teams for the execution and monitoring of clinical trials, as well as assist with data interpretation and communication to internal ...

Arcus Biosciences

$245K - $260K/yr

... study management team meetings. * Contribute to the preparation of key documents including ... clinical study protocols, study reports, and regulatory briefing documents. * As a lean but growing ...

Telix Pharmaceuticals (AMER)

OR

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 ...

Natera

OR

$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 ...

Natera

OR

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

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated ... You will oversee timelines, budgets, operational risks, study start-up activities, vendor ...

Syneoshealth

OR

Clinical Project Manager II - Early Phase Virology /Healthy Volunteer Studies (Sponsor Dedicated ... You will oversee timelines, budgets, operational risks, study start-up activities, vendor ...

Spyre Therapeutics

OR · On-site

$215K - $230K/yr

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 ...

Care Access

OR · On-site

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 ...

Syneoshealth

OR

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 ...

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

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 ...

Natera

Senior Clinical Scientist, ECD

OR · On-site +1

Demonstrated experience leading and executing clinical studies, including clinical data review, study-level decision making, issue management, and cross-functional coordination Preferred ...

Telix Pharmaceuticals (AMER)

OR

Strong understanding of drug development, clinical study design, regulations (CFR, FDA, EMA, and ... Strong project management skills. Organized and self-motivated. Strong attention to detail. Key ...

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Clinical Study Manager information

See Oregon salary details

$30

$66

$101

How much do clinical study manager jobs pay per hour?

As of Jul 27, 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.

Is CRC an entry level position?

A Clinical Research Coordinator (CRC) is often considered an entry-level role in clinical research, requiring basic knowledge of study protocols and good clinical practice (GCP). However, some positions may prefer prior healthcare or research experience, and advancement typically involves gaining additional certifications or experience. The role often serves as a stepping stone to more senior positions like Clinical Study Manager.

What are the key skills and qualifications needed to thrive as a Clinical Study Manager, and why are they important?

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.

Is CRA an entry level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, such as coordinating trials or working in related roles. Entry-level roles in clinical research often include Clinical Trial Assistant or Clinical Research Coordinator, while CRAs often need knowledge of Good Clinical Practice (GCP) and relevant certifications like CCRP or RAC.

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 budgets, and ensure data quality, often using specialized software and requiring strong organizational skills. Their role is essential for the successful completion of clinical research projects.

How much does a clinical trials manager make?

A clinical study manager typically earns between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior managers or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and responsibilities.
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 job categories do people searching Clinical Study Manager jobs in Oregon look for? The top searched job categories for Clinical Study Manager jobs in Oregon are:
What cities in Oregon are hiring for Clinical Study Manager jobs? Cities in Oregon with the most Clinical Study Manager job openings:
Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Oregon as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, 7% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $137,483 per year, or $66.1 per hour.
Senior Clinical Trial Manager

Senior Clinical Trial Manager

Natera

OR • On-site

Other

Posted 6 days ago

Natera rating

7.6

Company rating: 7.6 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories

Job description

POSITION SUMMARY:  

The Senior Clinical Trial Manager will be responsible for managing all aspects of clinical trials in the field of Oncology. The Clinical Trial Manager should have experience in managing all aspects of the trials independently, including study design, protocol implementation, site monitoring, and recruitment site management. Natera is dedicated to robust clinical trial design and execution, as demonstrating test ability and performance is essential to Natera's reputation and integrity. The candidate will work closely with Natera's clinical trials, R&D and scientific communications teams to accomplish this end.  

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

  • 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 requirement.

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

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

  • Mentor junior clinical operations staff and supervise clinical study team.

  • 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, or other relevant discipline required, Advanced degree preferred.

  • 5-8 years of clinical research experience, including at least 2-5 years of experience in managing clinical trials as a leading role.

  • Familiar with the FDA regulations relevant to clinical trials.

  • Experience in managing studies, CROs and sponsors is preferred.

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

KNOWLEDGE, SKILLS, AND ABILITIES:

  • 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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