Clinical Research Data Associate II - The Angeles Clinic & Research Institute
About The Position
The Clinical Research Data Associate II manages data for assigned research studies. Responsibilities include designing data-collection forms, abstracting and processing clinical data, maintaining record systems, and producing study reports. The associate may train clinical research staff, perform basic statistical analyses, and work with bioinformatics to develop and maintain trial management systems. The role ensures compliance with federal and local agency requirements, including those of the Food and Drug Administration (FDA) and the local Institutional Review Board. This is a hybrid position requiring four days per week onsite and one day per week remote. Fully remote arrangements are not available.
Requirements
- High school diploma or GED.
- At least two years of relevant experience in clinical research or a related setting.
- Hands-on experience with Electronic Data Capture (EDC) systems.
- Familiarity with EDC platforms such as REDCap, Oracle Clinical, Veeva Vault, Medidata Rave, and/or OpenClinica.
- Proficiency with data management software and related tools.
- Ability to work effectively in a collaborative, team-oriented environment.
- Strong attention to detail and excellent organizational and time-management skills.
- Excellent written and verbal communication skills.
- Ability to adhere to regulatory requirements and ethical guidelines.
Nice To Haves
- Bachelor’s degree in a related field, such as Life Sciences or Health Sciences.
- EDC experience, preferably within oncology clinical trials.
- Certification in Clinical Research (ACRP, SOCRA, or equivalent).
Responsibilities
- Coordinate data for research studies.
- Design forms for data collection.
- Perform clinical data collection and abstraction.
- Process clinical data using computer applications and database systems to support cleaning and management of subject or patient data.
- Produce project reports.
- Perform data searches and related administrative tasks.
- Participate in required training and education programs.
- Work with study monitors to review study data and respond to inquiries.
- Provide support and preparation for study audits.
- May train clinical research staff to improve the quality of collected data.
- May solve operational or data problems in consultation with other employees and/or supervisors.
- May perform basic statistical analysis in conjunction with a biostatistician.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
