Deva Rajan Subramanian Email & Phone Number

Chennai, Tamil Nadu, India

Chennai, Tamil Nadu, India

As a Rave Specialist, I am responsible for the following activities while adhering to Organization Vision, Mission and Motto:- Setup and Maintenance of Medidata Rave system including URL level upgrades/customization- Implementation and Maintenance of System Integrations (CTMS, IxRS)- Co-ordination and Implementation of Custom Scripts- Development of Listings and/or Reports- Preparation of Validation documents (Validation Plan, Validation Report)- Preparation and Execution of Validation Scripts- Validation and Documentation in adherence to SOPs, GCP and applicable regulatory requirements- Co-ordination and Support Internal/External stake holders on EDC System, Integrated Applications, Clinical DBs, Reports and Processing ToolsAs a Technical Expert, I am responsible for:- Leveraging technology in Implementation, Validation and Maintenance of tools and applications following GxP and Regulatory Processes

Chennai, Tamil Nadu, India

As a Clinical Study Database Designer lead I was responsible for : - Coordination with various stake holders of the trials (Onsite Team, Database Designers, Data Managers) - Delivery of DB Package consisting of Edit checks and Custom Functions - Documentation of Clinical Study Milestones, Meeting Minutes and Production Releases - Analysis of the Impacts in Post - Production Changes - Medidata Rave Report generation and Analysis - User Access Management - Clinical Views creation and refresh - Core Configuration managementBeing a technical programmer, my responsibilities were to : - Update myself with latest technologies - Implement Windows/Web/Azure Applications enhancing the efficiency of the processAs a Subject Matter Expert I perform the following activities : - Train associates in Programming with C# and RAVE Custom Function - Analyze and provide proactive solutions during Impact Analysis of Post Production changes in Study Setup

Paris Area, France

As an Onsite Database Designer, I was responsible for the following activities:- Coordination with various study team members (Data Managers, Trial Administrators, Medical Coders, Bio Statisticians and Study Setup Team)- Production implementation of eCRF Design, Dynamism/Derivations, Edit checks and Custom Functions- Post Production implementation through Migration and Publisher- Implementation of Auxiliary Systems - TSDV and Safety mails- Understanding of Core Configuration and RAVE Data Flow

Chennai Area, India

As a Clinical Study Database Lead Programmer I was responsible for :- Coordination with the Onsite Team for smooth and timely delivery of eCRF and DB Package using Medidata RAVE, Phase Forward Inform and ClinTrial with CIS Sync- Electronic Documentation of the various stages of the Clinical Trial- Post Production Change impact analysis

Chennai Area, India

I was trained in .NET and Java as a part of Dual Technology training at Cognizant. As a tester, I was responsible for the creation, execution and timely delivery of test cases for studies with eCRF and DB Package in Inform and ClinTrial systems

Bachelor Of Technology (B.Tech.), Information Technology, First Class

I completed by B.Tech Information Technology in SVCE. Graduated in the year 2013 with First class.

Computer Science, 94 Percent

I did my 11th and 12th there in CSE branch. Completed my schooling in the year 2009

Higher Secondary Education, Central Board Of Secondary Education, 80 Percent

I studied my Higher secondary education in The Hindu Senior Secondary School, Indira Nagar