TI Clinical Research Assistant 2 at Oregon Health & Science University in Portland, Oregon

Job Description:

Oregon Health & Science University

Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu.


TI Clinical Research Assistant 2

US-OR-Portland

Job ID: 2024-32405
Type: Regular Full-Time
# of Openings: 1
Category: Research
Portland, OR (Waterfront)

Overview

The TI Senior Clinical Research Assistant may be involved in all facets of clinical research, from initial clinical trial development through trial closure and project completion. Clinical research conducted within the Division of Pediatric Hematology/Oncology (PHO) includes cooperative groups (National Cancer Institute [NCI] or consortia sponsored), pharmaceutical (industrial sponsored), and local investigator-initiated clinical trials. This position requires independent performance of assignments of significant complexity. This position works with people at all levels of the organization and interacts with numerous internal OHSU departments and external customers (sponsors, monitors, referring physician offices). Duties and schedule may vary at any given time on an as-needed basis.

Under minimal supervision, coordinates complex therapeutic interventional clinical research protocols and data management. Contributes to feasibility assessment and research protocol management. Ensures research protocol implementation. Collaborates with various OHSU departments to complete protocol-required tests and procedures, which may include the research pharmacy, Epic informatics team, clinical research billing office, and other areas. Accurately applies investigators’ scientific data into a cohesive format for the protocol document and associated procedures that are consistent with internal and external policies and regulatory requirements. Coordinates projects with active management of expectations, timelines, and deliverables through facilitation and coordination of steps, which may include multiple clinical research protocols. Tracks and reports milestones. May assist leadership across multiple protocols to ensure appropriate and consistent project management, complex logistics, quality assurance, and participant safety. May lead data and regulatory audits of study conduct and data, emphasizing data security in concordance with federal, state, and local regulations. May participate in onboarding and training new staff.

Exercises judgment within defined Good Clinical Practice and HIPAA guidelines to determine appropriate action via reporting mechanisms and structures (Institutional Review Board) in recognizing adverse events, protocol deviations, and other unanticipated study problems and reports to senior staff appropriately.

Maintenance and submission of patient data and preparation for quality assurance audits and monitoring. Assist in preparation for inspections from Federal regulatory agencies. Data management on studies. May include eIRB and eCRIS/OnCore submissions.

Key Responsibilities:

• Gain familiarity with multiple therapeutic intervention clinical trials
• Determine potential study participants’ eligibility, facilitate informed consent process, enroll participants onto study through electronic databases
• Prompt study sample submissions (blood, bone marrow, tissue) via express mail
• Submission of participant data to consortia and pharmaceutical data bases including prompt required reporting of adverse events
• Regulatory functions (IRB interface) for industry sponsored trials

Responsibilities

Education & 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 abilities:

• Ability to type quickly and accurately on a QWERTY keyboard, moderate to advanced computer skills in Excel, Word, proficient with email and the Internet
• Ability to compile/organize and to keep clear, accurate, precise, complete and organized written and electronic records.
• Excellent written and verbal communication skills, including the ability to communicate effectively with medical personnel.
• Ability to work professionally within all levels of an organization and to work effectively both independently and as part of a team.
• Ability to learn quickly, retain, synthesize and apply information, follow detailed directions, and become proficient with appropriate systems and standard operating procedures.
• Excellent memory: long and short term, with quick recall for both text and numbers, math skills for clinical applications (ie % calculations, dose calculations, volume calculations).
• Strong independent analytical skills, meticulous attention to detail, and refined trouble-shooting skills.
• Familiarity with and application of medical terminology.
• Ability to work efficiently and effectively and meet deadlines in stressful, time-sensitive situations.
• A flexible style with excellent time management and multi-tasking skills and the ability to prioritize and organize a high-volume workload with a consistent high-quality work output.
• Ability to provide excellent customer support to internal and external clients.
• Ability to maintain confidentiality of information.
• Professional attitude and demeanor.

Qualifications

Education & experience:

• Major courses in sciences.

• Experience as a clinical research assistant in pediatric or medical oncology.

• Prior experience abstracting patient data from electronic medical records systems like EPIC.

Knowledge, skills, and abilities:

• Familiarity with medical terminology specific to pediatrics, hematology, oncology, and blood and marrow stem cell transplantation.
• Familiarity with Good Clinical Practices (GCP), HSR (Human Subjects Research), RCR (Responsible Conduct in Research).
• Familiarity with regulations related to clinical research.
• Familiarity with Quality Improvement, Quality Assurance and Quality Control.
• Preference will be given to an applicant who is SOCRA or ACRP certified.

PI255601247

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