TI Clinical Research Assistant 2

at  Oregon Health Science University

Department Overview:
As a Therapeutic Intervention Clinical Research Assistant 2, this individual is responsible for clinical, administrative, regulatory and educational research activities related to the management of patients on clinical trials. The appointee shall provide services as assigned by the supervisor in furtherance of the university’s missions and goals of teaching, research, patient care, outreach and public service. Appointee will participate in the on call schedule including intermittent evening, weekend, and holiday coverage. Position is Monday - Friday with weekend and holiday call coverage. Position may require travel to off-site partnership locations around the state of Oregon.

Function/Duties of Position:

• Clinical Trials Management
• Management of women’s health clinical research trials at OHSU and other affiliated hospitals including maintenance and submission of patient data, analysis and evaluation of protocol activities, maintenance and preparation for quality assurance audits and management of investigational drugs.
• Also includes all data management on assigned studies.
• Patient Contact
• Responsible for patient interactions as outlined in protocol and as delegated by Principal Investigator.
• Perform participant interviews and physical measurements, including but not limited to blood pressure, heart and respiratory rates, and specimen collection(s).
• Specimen processing as outlined by research protocol
• Regulatory Compliance and Administrative
• Maintenance and submission of patient data and preparation for quality assurance audits and monitoring.
• Data management on assigned studies
• Must be able to do data entry for extended periods of time.
• eIRB and eCRIS submissions.
• Outreach
• Assist in maintaining social networking sites, submitting blog and newsletter content, and other marketing or advertising outreach efforts as assigned and supervised by unit manager.

Required Qualifications:

• Bachelor’s in with major courses in field of research OR Associate’s AND 2 years of relevant experience OR 3 years of relevant experience OR Equivalent combination of training and experience
• Appreciating and cultivating a diverse study population. Excellent eye to detail and organization skills. Self starter.

Preferred Qualifications:

• Bachelor’s degree
• Clinical Trials experience strongly preferred.
• Women’s Health specific experience is preferred. 1-2 years research experience preferred.
• Previous work with physicians in an academic environment. Epic, Outlook, eIRB, OHSU systems.
• Spanish speaking

Additional Details:
Upload cover letter and resume. Please be sure to include months and years to the resume for jobs/experience.
All are welcome: 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 Trials Management
• Management of women’s health clinical research trials at OHSU and other affiliated hospitals including maintenance and submission of patient data, analysis and evaluation of protocol activities, maintenance and preparation for quality assurance audits and management of investigational drugs.
• Also includes all data management on assigned studies.
• Patient Contact
• Responsible for patient interactions as outlined in protocol and as delegated by Principal Investigator.
• Perform participant interviews and physical measurements, including but not limited to blood pressure, heart and respiratory rates, and specimen collection(s).
• Specimen processing as outlined by research protocol
• Regulatory Compliance and Administrative
• Maintenance and submission of patient data and preparation for quality assurance audits and monitoring.
• Data management on assigned studies
• Must be able to do data entry for extended periods of time.
• eIRB and eCRIS submissions.
• Outreach
• Assist in maintaining social networking sites, submitting blog and newsletter content, and other marketing or advertising outreach efforts as assigned and supervised by unit manager