Clinical Research Assistant I

Portland VA Research Foundation•Portland, OR

4d•Onsite

About The Position

Clinical Research Assistants support the implementation of clinical trials by conducting study visits, preparing participant materials, collecting data, and helping ensure studies are well organized and in compliance with protocols. This role offers direct exposure to patient interactions, clinical workflows across multiple medical specialties, and regulatory processes. Research Assistants work closely with Study Coordinators, Principal Investigators, clinicians, and patients, gaining valuable experience that can serve as a strong foundation for advancement into Study/Project Coordinator roles and beyond. Responsibilities provide meaningful opportunities for hands-on learning and professional development in both research and healthcare, while supporting Veterans and their caregivers. We are seeking a dedicated Clinical Research Assistant to take primary responsibility for multiple aspects of human subjects research with Veteran patients. Our current research includes prostate, bladder, hematologic, gastrointestinal, and skin cancer clinical trials. This position involves direct patient interaction in a clinical setting with prospective and retrospective data collection. This position is located in the Research and Development Service of the VA Portland Health Care System (VAPORHCS) in Portland, Oregon.

Requirements

Bachelor's degree
English language proficiency with excellent oral and written communication skills
Must be able to count, calculate, interpret numerical data/graphs and perform basic mathematical calculations
Proficiency with Microsoft Office (Word, PowerPoint, Excel & Outlook)
Ability to communicate effectively and professionally via email, MS Teams Chat and other electronic platforms
Strong critical thinking and problem-solving skills as well as deductive and inductive reasoning abilities
Ability to independently meet deadlines, anticipate needs, prioritize multiple tasks, and follow through on tasks to completion
Excellent organizational skills with high attention to detail and accuracy
Ability to work independently, exhibit self-motivation and enthusiasm to learn new skills
Take initiative to identify and address issues and concerns of veteran patients in a timely and caring manner

Nice To Haves

Degree in science, social science, or other health related fields
Prior research experience, either volunteer, academic or professional
Basic statistical, data interpretation and unit conversion knowledge
Prior experience using Electronic Data Capture (EDC) systems such as REDCap, Medidata, or Inform

Responsibilities

Ensure the proper conduct of clinical trials according to protocol requirements
Recruit and communicate with Veteran participants in a clinical setting and by phone
Accurately screen, consent, and enroll eligible Veteran patients into clinical trials
Precisely and accurately document and organize source materials into patient records and electronic medical record systems (EMR)
Develop databases, participant tracking systems, and standard operating procedures for research projects
Accurately, thoroughly, and respectfully solicit health information from Veteran participants within a clinical setting and by phone
Ensure timely data collection, entry, auditing, and query resolution
Collect and ship research biospecimens
Manage Electronic Data Capture (EDC) across multiple trials and confirm participant timepoint completion
Work independently under general supervision of Principal Investigator and ensure tasks are completed accurately and on time.
Communicate any problems and concerns, and suggest solutions to the Program Manager, and/or appropriate Principal Investigator.