Clinical Research Data Specialist I (Hybrid)

Primary Duties And Responsibilities

• Manages and maintains research data to ensure accuracy, integrity, and security of complex, large computerized records systems.
• This includes performing data searches and other related administrative tasks.
• Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.
• Designs forms for data collection and performs clinical data collection/abstraction.
• Produces project reports for research studies.
• Understands regulations, policies, protocols and procedures to control and maintain accurate records.
• Safeguards compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
• Maintains research practices using Good Clinical Practice (GCP) guidelines.
• Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
• Participates in required training and education programs.

Qualifications

• This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week.
• If hired you must reside in the commutable area.
• Education: High school diploma or GED required; BA/BS in a related field preferred.
• Work Experience: 1 year of experience related to the field of research required.