* Collect project data through interviews, chart review or other methods. * May collect, secure and assist with biospecimen management. * 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.
Top Skills: Strong data entry, strong attention to detail skill, medical terminology, Microsoft Suite
Desired skills: Orthopedic terminology, EPIC experience, Access experience
Basic Qualifications: * Minimum one (1) year of experience in public health, healthcare administration, epidemiology, or healthcare-related field.
* High School Diploma or General Education Development (GED) required.
* Bachelor's degree preferred- in public health, healthcare administration, epidemiology, or health-related field (ex. Biology, Psychology, etc.), OR four (4) years of experience in a directly related field. **(TITLE) RESEARCH ASSOCIATE I****
* Experience with interviewing (by phone and/or in-person) and medical chart review. * 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.