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.


Clinical Research Assistant 2

US-OR-Portland

Job ID: 2024-32188
Type: Regular Full-Time
# of Openings: 1
Category: Research
Portland, OR (Waterfront)

Overview

Key Responsibilities:

• Clinical Trial Coordination
  • Work with the regulatory management team and colleagues to adhere to regulations at OHSU for good clinical practices and clinical trials.
  • Be knowledgeable about clinical research protocols and protocol requirements.
  • Distribute clinical research-related information to the appropriate research team / affiliated institutional personnel as applicable. Notify the research team and those individuals directly involved in in pertinent areas of clinical research of protocol amendments, revisions, activations, closures, and announcements.
• Participant Coordination
  • Participate in recruitment activities to include community outreach and flyer distribution, including some weekend and evening events.
  • Contact and enroll subjects by reviewing patient data to determine appropriate eligibility and scheduling eligible participants.
  • Conduct study visits in adherence with protocol parameters and appropriate training, including consenting, taking a medical history, and the procurement and processing of human biological specimens. Obtain and submit imaging studies, pathology samples as required by sponsor to appropriate reviewers as required by protocol. Review and report adverse events or unanticipated Problems to IRB/study sponsor.

Responsibilities

Education & experience:

• Bachelor's in relevant field OR
• Associate's AND 2 years of relevant experience OR
• 3 years of relevant experience OR
• Equivalent combination of training and experience

Knowledge, skills, and abilities:

• Demonstrated excellent customer service experience
• Experience with Microsoft Office
• 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
• Excellent customer service, both on the phone and in person
• Energy and drive to coordinate multiple projects simultaneously
• Ability to use tact and diplomacy to maintain effective working relationships
• Keen attention to detail
• Strong trouble shooting skills
• Ability to become phlebotomy trained within first 6 months

Qualifications

• Some clinical trial knowledge and research experience
• Experience with database systems
• Experience with medical terminology
• Experience in a medical environment
• Bilingual

PI254524961

Apply Now