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Study Manager Jobs in Oregon (NOW HIRING)

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TI Sr Clinical Research Assistant

Portland, OR · On-site

$70 - $100/hr

The support is provided through proactive, high quality and efficient study management in compliance with federal regulations and local policies and procedures. This fast‑paced and highly intense ...

Natera

Manager, Clinical Trials

OR · On-site +1

Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites * Lead study-related activities such as protocol and ...

Phoenix-Talent Schools

Social Studies Teacher

Phoenix, OR

$46K - $63K/yr

Social Studies Teacher - Talent Middle School APPLICATION PROCEDURES: Interested candidates must ... Deliver instruction, effectively manage the classroom environment, meet all other professional ...

Phoenix Talent Schools

Social Studies Teacher

Talent, OR · On-site

$46K - $62K/yr

Social Studies Teacher - Talent Middle School APPLICATION PROCEDURES: Interested candidates must ... Deliver instruction, effectively manage the classroom environment, meet all other professional ...

Stride, Inc.

High School Social Studies Teacher

OR · On-site +1

$17 - $20/hr

Teachers monitor student progress through Stride's learning management system, and work actively ... The Social Studies Teacher is a highly qualified, state certified educator responsible for ...

Blattner Company

Lead Engineer - Studies

OR · On-site +1

$121K - $176K/yr

Serve as the primary study point of contact for owners and EOR teams and review third-party study ... Demonstrated experience leading studies programs and managing staff across a portfolio of ...

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Study Manager information

See Oregon salary details

$25.9K

$62.9K

$122.6K

How much do study manager jobs pay per year?

As of Sep 6, 2026, the average yearly pay for study manager in Oregon is $62,935.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,400.00 and $72,400.00 per year, depending on experience, location, and employer.

What does a study manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.

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

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

How does a study manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What is the role of a study manager?

A study manager oversees the planning, execution, and completion of clinical or research studies, ensuring they adhere to protocols, timelines, and regulatory requirements. They coordinate with teams, manage budgets, and monitor progress using tools like project management software to ensure study objectives are met efficiently.

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

The most popular types of Study jobs in Oregon are:

Study Manager jobs near you
Infographic showing various Study Manager job openings in Oregon as of June 2026, with employment types broken down into 95% Full Time, 4% Part Time, and 1% Temporary. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $62,935 per year, or $30.3 per hour.

Coordinator II, Clinical Research

Shriners Children's Hospital

Portland, OR • On-site

$61 - $91/hr

Other

Posted 4 days ago

Job description

## Coordinator II, Clinical ResearchApplyremote type: On-Sitelocations: Portland, ORtime type: Full timeposted on: Posted Yesterdayjob requisition id: JR101183**Company Overview**Shriners Children’s is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family’s ability to pay or insurance status. Please click here to learn more about our locations.**Job Description**Shriners Children's Portland is seeking a full-time Clinical Research Coordinator II to join our team! The Clinical Research Coordinator is a specialized, independent research professional who ensures oversight and compliance of both system-wide and local SHC clinical research activities. The CRC provides support in accordance with our policies and procedures, hospital regulations and the Code of Federal Regulation and Good Clinical Practice guidelines. The CRC works closely with the Chief of Staff, SHC scientific and medical staff and other research personnel to ethically recruit and consent SHC’s vulnerable pediatric subjects and to appropriately collect and safeguard data. Overall, the CRC is the site’s primary liaison among research participants, the local investigator(s) and study sponsor(s). This position’s main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.**Key Responsibilities:*** Maintains a contemporary knowledge of clinical research regulatory requirements. Has a working knowledge of the complex clinical research process, from protocol development to implementation.* Works closely with investigators, research leadership, study sponsor and regulatory agencies to conduct and report the results of clinical research.* Coordinates both system-wide and local SHC clinical research activities* Provides support in accordance with SHC's policies and procedures, SHC's hospital regulations, the Code of Federal Regulation and Good Clinical Practice guidelines, when applicable* Act as primary liaison among research participants, the local investigator(s) and study sponsor(s)* Ensure proper study conduct, subject safety, and the quality of data and data safeguards* Subject recruitment and data/specimen collection of SHC's system-wide projects.**Required Qualifications:*** 3 or more years Clinical research experience, e.g. experience with site management, study management, IRBs, and federal regulations regarding clinical research compliance* Without a Bachelor's degree, 5 or more years of specific job-related experience in the administration of clinical research**Preferred Qualifications:*** Bachelor’s in Clinical Research, science or other health-care-related field* Master's Clinical Research, science or other health-care related field* Experience in the coordination of intergroup or multi-site clinical studies* CCRP or CCRC certificationThe pay range for this position is $60,815.04 - $91,199.68. Compensation is determined based on years of relevant experience and departmental equity. #J-18808-Ljbffr

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