
Leading Edge Cdm Solutions
Biotechnology, 700 Promontory Pt Ln, Foster City, California, 94404, United States, 11-50 Employees
Who is LEADING EDGE CDM SOLUTIONS
WITH US, IT'S ALWAYS PERSONAL. We are experts in end-to-end clinical data management. Founded in 2014, LeCDMS has become a trusted partner to its clients, ranging from small to medium-siz...
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Headquarters: 700 Promontory Pt Ln, Foster City, California, 94404, United States
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Date Founded: 2014
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Employees: 11-50
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Revenue: Under $1 Million
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Active Tech Stack: See technologies
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CEO: Gina Budman
Industry: Biotechnology
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Leading Edge CDM Solutions Org Chart and Mapping
Paulette Roper
Sr. Director, Clinical Data Management and Quality Systems Representative
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Frequently Asked Questions Regarding Leading Edge CDM Solutions
Answer: Leading Edge CDM Solutions's headquarters are located at 700 Promontory Pt Ln, Foster City, California, 94404, United States
Answer: Leading Edge CDM Solutions's official website is https://leadingedgecdmsolutions.com
Answer: Leading Edge CDM Solutions's revenue is Under $1 Million
Answer: Leading Edge CDM Solutions has 11-50 employees
Answer: Leading Edge CDM Solutions is in Biotechnology
Answer: Leading Edge CDM Solutions contact info: Phone number: Website: https://leadingedgecdmsolutions.com
Answer: WITH US, IT'S ALWAYS PERSONAL. We are experts in end-to-end clinical data management. Founded in 2014, LeCDMS has become a trusted partner to its clients, ranging from small to medium-sized biotechnology, pharma, and medical device companies. WHY US: As a lean boutique company we avoid bureaucracy and are focused on your success by providing quality personalized services: - We provide any DM related services on an as-needed basis. - You will work directly with a project manager who is an expert in your study. The PM will ensure that your study will have the team's full attention no matter how big or small it is. - We hire only experts. You will always get an A team that knows your trial from study start-up to submission. - To lower budget requirements, we utilize modern technology and engage cost-effective resource allocation. DATA MANAGEMENT / CLINICAL DATA ADVOCATES - CRF/eCRF design - Setting up data validation checks - EDC User Acceptance Testing - Data query management - Data entry - Monitoring data support (we prepare the Monitors for their visits, and support while they are at the site) - AE/SAE reconciliation - Medical coding (MedDRA, WHO Drug) - Device accountability - Compliant Data management documentation (DM Plan, Data Transfer Agreements, CRF/eCRF guidelines) - Data listings, metrics, and reporting EDC PROGRAMMING / CLINICAL DB EXPERTS - EDC/other supporting software selection - Database build in a variety of platforms - Database amendments and migrations - Database validation - EDC training - User and site management - Lab and other data uploads SAS PROGRAMMING / SAS-PROS - Statistical Analysis Plan - Analysis dataset specifications - Develop and validate SAS programs - Tables, Listings, and Figures - Data Extracts and Reports - CDISC SDTM, SEND and ADaM data conversion - CDISC documentation - Ad hoc or exploratory programming BIO STATISTICS / HI-BIOSTATS - Protocol Statistical section - Study randomization - Sample size determination - Statistical Analysis Plan - Statistical Programming Plan - Oversee SAS programming - Statistical analysis & reporting - Biostatistical consulting - Investigator meetings - Support for regulatory submissions CLINICAL IT / CLINICAL IT MASTERS - Vendor assessment and advising on technology - Solution Architecture, Design, and Development - Mobile, AI/ML Intelligence, and Enterprise Applications - System integration - Validation and Q&A including automated testing - Training, support, and reconciliation
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