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Clinical Research Data Manager Jobs in Oregon (NOW HIRING)

Data management duties include ensuring accurate and complete research data is collected from oncology clinical trial study subjects and entered into the appropriate Case Report Forms. This role will ...

Provide senior technical leadership and oversight for data management and programming activities across clinical, observational, and epidemiologic research studies, from study start-up through ...

This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate ... Data Management * Collection and entry of oncology data from patient medical records into study ...

What You'll Do * Lead data management for complex, global clinical trials from study setup to ... Strong understanding of GCP, ICH, and clinical research processes. * Excellent communication and ...

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Clinical Research Data Manager information

See Oregon salary details

$51.8K

$113.5K

$199.8K

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

As of Sep 6, 2026, the average yearly pay for clinical research data manager in Oregon is $113,485.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,600.00 and $129,500.00 per year, depending on experience, location, and employer.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.

What are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

What are the key skills and qualifications needed to thrive as a clinical research data manager, and why are they important?

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

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

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

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

The most popular types of Clinical Research Data jobs in Oregon are:

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

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

What cities in Oregon are hiring for Clinical Research Data Manager jobs?

Cities in Oregon with the most Clinical Research Data Manager job openings:

Infographic showing various Clinical Research Data 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 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $113,485 per year, or $54.6 per hour.

TI Sr Clinical Research Assistant

UNAVAILABLE

Portland, OR • On-site

$70 - $100/hr

Other

Posted 5 days ago


Key responsibilities

  • Coordinate complex therapeutic interventional clinical research protocols and manage study data and regulatory components.

  • Oversee the oncology study start-up process, including tracking start-up metrics, developing consent forms, and managing submissions and communications with regulatory bodies.

  • Ensure accurate collection, entry, and quality control of research data from oncology clinical trial subjects.


Job description

Department Overview

The mission of the Knight Clinical Research Management organization is to support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening diagnosis and treatment. 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 research environment require management of complex clinical research studies involving a very vulnerable and sick population.

Function/Duties of Position

This OHSU Knight Cancer Institute TI Sr. Clinical Research Assistant (TI Sr. CRA) is responsible for the collection, entry, general management of oncology study data and all regulatory components for oncology clinical trials. Under minimal supervision, coordinates complex therapeutic interventional clinical research protocols and data management.

This position has ownership of the oncology study start-up process, including the tracking of oncology clinical trials start-up metrics, communicating with all start-up process owners and participants, consent form development, CRRC and IRB submissions and all communications/ responses, CTRP registration workflows, flowsheet updates, and VIA Oncology updates. In addition, the position also has oversight over the feasibility assessment, essential regulatory document completion, beacon build, eCRIS, and budget and contract negotiation processes. The position also has ownership of all regulatory tasks that must be completed over the lifetime of the oncology clinical research studies they support, including the processing of protocol amendments, investigator brochures and safety reports, consent form updates, and applications for continuing approvals.

Data management duties include ensuring accurate and complete research data is collected from oncology clinical trial study subjects and entered into the appropriate Case Report Forms. This role will also assist with the coordination of oncology clinical trial monitoring visits, data query resolution, and quality control of collected research data.

This position must maintain a working knowledge of oncology data, a vast variety of differing electronic database systems, a working collaboration with our internal and external partnerships, of FDA, DHHS and other agency guidelines that govern clinical research.

* Therapeutic Interventional trials are treatment studies that involve people who have a disease or underlying condition. They include the administration and testing new treatments or new ways of using existing treatments, such as new drugs, vaccines, cell therapies, devices, experimental approaches to surgery or radiation therapy, etc.

OHSU Research classification: TI Sr. Clinical Research Assistant, represented by the Research Workers United (RWU), subject to the active collective bargaining agreement between OHSU and RWU.

Required Qualifications

Education and experience:

Bachelor's Degree in relevant field AND 1 year of relevant experience OR

Associate's AND 3 years of relevant experience OR

4 years of relevant experience OR

Equivalent combination of training and experience.

Knowledge, skills, and ablitilites:

  • Commitment to overall data integrity with ability to communicate and advocate for data quality
  • High degree of attention to detail
  • Ability to clearly organize and/or adapt to multiple priorities and tight deadlines at one time
  • Ability to follow through and complete tasks
  • Ability to track progress and update others on status of data collection
  • Strong innovation and problem solving
  • Excellent communication, analytical and organizational skills: both written and verbal.
  • Ability to work independently and as part of a team, while being collaborative in resolving problems
  • Proficient with computers running Windows and PC applications e.g. MS Excel, Oracle, Access, Word and PowerPoint
  • Ability to generate a variety of reports in MS Word and Excel
  • Ability to use tact and diplomacy to maintain effective working relationships
  • Adaptability
  • Strong critical thinking skills
Preferred Qualifications
  • Strong understanding of the scientific method
  • Demonstrated project management skills or project management experience
  • Demonstrated customer service skills or customer service experience

All are welcome. OHSU welcomes people of all ages, ethnicities, genders, national origins, religions and sexual orientations. We are striving to build an anti‑racist, multicultural institution and encourage people with diverse backgrounds to apply. To request reasonable accommodation, contact askhr@ohsu.edu

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