Clinical Research Data Associate II - The Angeles Clinic & Research Institute

Cedars-Sinai Medical Center•Los Angeles, CA

1d•Hybrid

About The Position

The Clinical Research Data Associate II manages data for assigned research studies at The Angeles Clinic & Research Institute. The role includes designing data-collection forms, collecting and abstracting clinical data, processing data, maintaining record systems, and producing study reports. The associate may also train clinical research staff, perform basic statistical analysis, and collaborate with bioinformatics to develop and maintain trial management systems. The position ensures compliance with applicable federal and local requirements, including those of the 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 work 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, preferably in oncology clinical trials.
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.
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.
Support and prepare for study audits.
Train clinical research staff to help improve the quality of collected data, as needed.
Resolve operational or data problems in consultation with other employees and/or supervisors, as needed.
Perform basic statistical analysis in conjunction with a biostatistician, as needed.
Ensure compliance with applicable federal and local agencies, including the FDA and local Institutional Review Board.