Divya Ganesan
Clinical Data Manager @Sarah Cannon Research Institute
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WORK HISTORY
Clinical Data Manager @Sarah Cannon Research Institute
Phoenix, AZ, US
Lead cross functional Data Science teams (Statisticians, Programmers, Data Manager) to plan for anddeliver all data deliverables. This includes creating and managing all timelines and project plans and promoting effective team work among members of the data science team• Lead Data Science activities for 4-8 clinical trials. This includes but is not limited to: o CRF design o Database design and testing o Report specifications and testing o Data Management Plan development o Development of data quality checks o Management of data sources from outside vendors o Delivery of a locked database o Management of all mid-study changes to the database• Represent Sarah Cannon Development Innovations (SCDI) Data Science externally in Business Development activities• Represent SCDI Data Science in the development and implementation of internal process improvement initiatives• Participate in the training/mentoring of junior staff, including Clinical Data Analysts (CDA)• Direct the activities of CDAs• Key liaison with client to ensure the highest possible customer service in order to win repeat business• Enforce data standards with project team, physicians and clients• Identify data science scope changes and provide cost analysis to the project manager for these scope changes• Accountable for compliance to all SOPs and regulatory requirements• Accountable for ensuring all required documentation is created and filed in the Trial Master File
EDUCATION
Rollins School of Public Health at Emory University
Master of Public Health - MPH, Epidemiology
UCSC Silicon Valley Extension
Clinical Trials Design and Management
SRM College
Bachelor of Science (B.Sc.), Microbiology, General
Bharathidasan University
Master of Science (M.Sc.), Microbiology, General
SKILLS
ABOUT DIVYA GANESAN
As a Clinical Data Manager at Sarah Cannon Research Institute (SCRI), I lead cross-functional data science teams to plan and deliver data deliverables for oncology clinical trials. I have over 6 years of experience in clinical data management, with competency in various electronic data capture (EDC) systems, such as Medidata Rave and Oracle InForm, and statistical programming tools, such as SAS and R.My mission is to ensure the accuracy, quality, and integrity of data for clinical trials. I have extensive experience in the entire data management lifecycle, from CRF design and database testing, to data quality checks and database lock. I also have strong communication and project management skills, which enable me to collaborate effectively with sponsors, vendors, and study teams, and to oversee all data management processes and documents for assigned studies.
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