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TI Clinical Research Associate (Data Manager)

Job

Oregon Health & Science University

Portland, OR (In Person)

Full-Time

Posted 8 weeks ago (Updated 2 days ago) • Actively hiring

Expires 6/21/2026

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Job Description

TI Clinical Research Associate (Data Manager) at Oregon Health & Science University TI Clinical Research Associate (Data Manager) at Oregon Health & Science University in Portland, Oregon Posted in 4 days ago.
Job Description:
TI Clinical Research Associate (Data Manager)
US-OR-Portland Requisition ID:
2026-38529
Position Category:
Research Job Type:
Research Position Type:
Regular Full-Time Posting Department:
Knight Cancer Institute Posting Salary Range:
$60,673.60 - $101,129.60 per year, with offer based on education, experience, and the collective bargaining agreement with
RWU Posting FTE:
1.00
HR Mission:
School of Medicine Drug Testable:
Yes 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 TI Clinical Research Associate (focused in Data Management) is responsible for the collection, entry, and general management of oncology study data for oncology clinical trials. Under occasional supervision, coordinates complex therapeutic interventional clinical research• protocols and data management. Primary 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 clinical trial monitoring visits, data query resolution, and quality control of collected research data. The successful candidate will have and maintain a working knowledge of oncology data, a vast variety of differing electronic database systems, and a working collaboration with our internal and external partnerships. Strong communication skills and attention to detail are required. Ability to clearly organize and/or adapt to multiple priorities and tight deadlines at one time are necessary. Requires limited supervision; innovation and problem solving required; adaptability and a commitment to overall data integrity with ability to communicate and advocate for data quality. Given the complexities of oncology research and the challenges of working with a terminally ill population, strong customer service, organizational, and interpersonal skills are required. Ability to clearly organize and/or adapt to multiple priorities and deadlines at one time is necessary. Attention to detail, service orientation, delegation and project management skills, and above average critical judgment skills are essential.
Required Qualifications Education and experience:
Master's Degree in relevant field AND 3 years of clinical research coordination experience OR Bachelor's Degree in relevant field AND 5 years of clinical research coordination experience
Knowledge, Skills, & Abilities:
Ability to prioritize multiple tasks at one time 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 Proficiency with computers running Windows and PC applications e.g. MS Excel, Word and PowerPoint. Excellent customer service skills Energy and drive to coordinate multiple projects simultaneously Ability to use tact and diplomacy to maintain effective working relationships SoCRA or ACRP required within 12 months of hire Preferred Qualifications Bachelor's degree with coursework in science or related field One year of research experience, with some knowledge of clinical trials Experience conducting different phases of projects, including data collection Microsoft Office, Access, and other networking and database systems Medical terminology OHSU systems Oracle and/or Epic CCRP Equal employment opportunity, including veterans and individuals with disabilities.
PI283403027
Salary:
$60.00

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