Aleny Caban
About Aleny Caban
Aleny Caban serves as the Associate Director of Clinical Data Management at Kite Pharma, bringing extensive experience in clinical data roles across various pharmaceutical companies, including Astellas Pharma and Takeda Pharmaceuticals. With a strong background in oncology and expertise in Electronic Data Capture and CDISC Standards, Caban has developed a solid foundation in managing clinical trial data.
Work at Kite Pharma
Aleny Caban currently serves as the Associate Director of Clinical Data Management at Kite Pharma, a position she has held since 2021. In this role, she oversees the management of clinical data, ensuring accuracy and compliance with regulatory standards. Her expertise in oncology and clinical data management supports the company's focus on innovative cancer therapies.
Previous Experience at Astellas Pharma US
Prior to her role at Kite Pharma, Aleny Caban worked at Astellas Pharma US in various capacities. She served as Associate Director of External Data Operations from 2016 to 2019 and as Associate Director of the Enterprise Data Management Program Lead from 2019 to 2021. Additionally, she held positions as Senior Manager (Team Lead) in Data Management Programming and Specialty Data, and as Senior Data Management Programmer, contributing to her extensive experience in clinical data management.
Background in Clinical Data Management
Aleny Caban has a comprehensive background in clinical data management, beginning her career at Searle as a Clinical Database Administrator from 1997 to 2001. She continued to develop her skills at Takeda Pharmaceuticals, where she held multiple roles, including Project Data Management Programmer and Senior Database Programmer. Her experience spans over two decades in the pharmaceutical industry, focusing on oncology and data quality.
Education and Expertise
Aleny Caban holds a Bachelor of Science in Computer Science with a focus on Information Systems from DePaul University. This educational background provides her with a strong technical foundation for her roles in clinical data management. She possesses expertise in Electronic Data Capture (EDC) and CDISC Standards, both essential for maintaining data integrity in clinical trials. Additionally, her experience in CRO Management enhances her ability to oversee clinical trial execution effectively.