Clinical Research Assistant (Redmond, WA)

SUMMARY

The Research Assistant (RA) is responsible for the operational and administrative support for the day-to-day execution of multiple clinical trials.

This position collaborates with Research Coordinators, Regulatory, and other clinical research staff.

ESSENTIAL DUTIES

• Provide operational and administrative support for the day-to-day execution of multiple clinical trials
• Consent patients for clinical research studies with no supervision by Research Coordinator
• Create patient files and charts for studies
• Perform vital signs, nasal swabs, blood processing as needed for accurate study enrollments Enter data into electronic data capture (EDC) systems for patient enrollments and medical history
• Answer queries within EDC system in a timely manner
• Direct involvement in shipping not limited to packing, creating manifest, and communicating with the sponsor on shipping and/or receiving information
• Coordinate and process lab supplies
• Evaluate overall performance by gathering, analyzing, and interpreting data and metrics
• Develop relationships with external partners and vendors
• Follow established SOPs, GCP and other applicable regulatory requirements in the execution of all research activities

WORK ENVIRONMENT

• Clinical office environment
• May involve some exposure to hazards or physical risks, which require following basic safety precautions
• Occasional night and weekend work schedules may be required

PHYSICAL DEMANDS

• Frequent use of keyboard and mouse
• Frequent use of computer monitors and other electronic screens
• Frequent standing, walking, bending, and stooping
• Occasional ability to lift 10 pounds
• Ability to differentiate colors according to study protocols

EDUCATION & EXPERIENCE:

REQUIRED

• High School Diploma or Equivalent
• High attention to detail
• Outstanding patient care skills
• Ability to work independently with minimal supervision
• Ability to effectively collaborate with other team members
• Strong organizational and time management skills
• Excellent written and verbal communication Skills
• Experience with Microsoft Office

PREFERRED

• Associates degree
• MA-R and/or MA-P
• Phlebotomy license and experience
• 1 year of experience with clinical research
• Knowledge of clinical research operations, including Good Clinical Practice guidelines.

TRAVEL

At least 5% travel within the geographic region of the assigned work location.

OTHER DUTIES

In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.

EEO STATEMENT

ERA Health Research (ERA) provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on ERA. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.