Clinical Research Assistant NES

Davita Inc.; Providence (RI); On-site; USD 40,000 - 55,000; Full time

Job summary

A well-known health organization seeks a Clinical Research Assistant to support various research activities at Rhode Island Hospital. The role involves coordinating with physicians, conducting patient interviews, and managing data collection. Ideal candidates will have a Bachelor's degree in a related field and some on-the-job research experience, making this an excellent entry-level opportunity.

Qualifications

• Bachelor's Degree, coursework in research methodologies.
• 3-6 months of experience with specific research studies.
• Familiarity with data entry and computer systems.

Responsibilities

• Assist with clinical research activities and participant coordination.
• Monitor protocol adherence and manage study records.
• Conduct patient interviews and perform relevant research procedures.

Skills

Research methodologies

Organizational skills

Interpersonal skills

Analytical skills

Technical ability

Education

Bachelor's Degree in Applied or Life Sciences

Job description

Summary:
Under the general supervision of the Principal Investigator(s) and Clinical Research Coordinator, assist in the acquisition and analysis of patient information for multiple clinical research projects. Conduct patient interviews to gather information, prepare and maintain study records, enter data via computer, and perform statistical analyses of the data. Participate in qualitative and quantitative analyses, review relevant literature, and assist in developing research protocols. May perform EKGs, take vital signs during research-based monitoring tests, and handle blood spinning and shipment of blood and tissue samples as required by protocol.

Responsibilities:

• Assist Principal Investigators in coordinating clinical research activities related to the department's field of study and specific research projects.
• Support research physicians in identifying and following up with patients meeting study criteria, ensuring protocol eligibility.
• Establish and maintain study records for each participant, including conducting patient interviews, explaining the study, obtaining informed consent, and scheduling appointments.
• Review medical records to abstract necessary information and follow up on missing data.
• Monitor adherence to protocols, alert physicians of deviations such as missed tests or medication non-compliance.
• Perform research-based procedures such as EKGs, vital signs, blood spinning, and shipping in accordance with protocol specifications.
• Organize and facilitate data collection, entry into databases, and perform computer-assisted statistical analyses.
• Assist in planning research protocols and coordinate activities of team members involved in the research project.
• Review relevant literature to support research understanding and development.

Other information:

• Basic Knowledge: Bachelor's Degree in Applied or Life Sciences or related field, including coursework in research methodologies and microcomputer systems.
• Experience: 3-6 months of on-the-job experience with familiarity in specific research studies.
• Knowledge of research methodologies, organizational skills, interpersonal skills, analytical skills, and technical ability to operate and maintain computer systems.
• Demonstrated understanding of patient care considering aging, human development, and cultural patterns.

Brown University Health is an Equal Opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, ethnicity, sexual orientation, ancestry, genetics, gender identity or expression, disability, protected veteran status, or marital status. Brown University Health is a VEVRAA Federal Contractor.

Location: Rhode Island Hospital, Providence, RI, USA

Work Type: Full Time

Shift: Shift 1

Union: Non-Union

Apply now.