Research Associate I

• Collect project data through interviews, chart review or other methods.
• Set up tracking tools, assist in develop forms and document procedures.
• Monitors and tracks study over time and provides follow-up as needed.
• Summarizes data for progress reports.
• Orient and provide training to team members and/or clinical staff on specific project tasks.
• If assigned to clinical trial, may work with monitors at clinical sites.
• Adheres to compliance and privacy/ confidentiality requirements and standards.
• Adheres to GCP and compliance regulations for clinical trials.
• Responsible for reviewing own work to ensure data quality.
• Acquires and maintains knowledge of KP systems and databases.
• Identifies study issues and collaborates with team members to develop and implement solutions.
• Serves as a member on department or study-related committees.
• May assist with tracking information for invoices.

• N/A

• Bachelors degree

• N/A

• Ability to identify and solve problems.
• Team-focused, detailed and goal-driven with professional oral and written communication skills.
• Must be able to work in a Labor/Management Partnership environment.

• Experience with interviewing (by phone and/or in-person) and medical chart review.
• Minimum one (1) year of experience in public health, healthcare administration, epidemiology, or healthcare-related field.
• Proficiency in additional languages relevant to study populations (e.g., Spanish, Tagalog).
• Experience working with, or demonstrated familiarity with, the communities served by the studies.

Notes

Typical working days are Monday through Friday, though some study activities will also take place on weekends or evenings.