Description
To perform a wide range of Clinical Data Management activities resulting in high quality database within stipulated timelines. To provide expertise in programming concepts to the Data Management team RESPONSIBILITY Perform and/or initiate comprehensive data management tasks, pertaining to Data base design, programming, Validation and Data transfers Perform quality control procedures for Database Design and Database Programming. Assist in developing and implementing new technology in Database Design. Provide Clinical Data Management team with technical expertise Develop and maintain good communications and working relationships with CDM team. Review the contract, protocol and any other customer specifications for implementing any client specifications Perform tasks/activities as communicated by TL/LDM Create/review the Data Management Plan documents Attend telephone conferences/meetings as required Adherence to SOPs/Regulatory requirements/project specific guidelines Escalation of identified unresolved issues to Lead Data Manager on time Provide inputs/status reports on monthly basis during the tenure of life cycle of the project PREFERRED EDUATION Bachelors/Masters in Sciences or equivalent Qualifications PREFERRED EXPERIENCE Preferred minimum 1-3 years of experience in any CDMS application Excellent interpersonal and communication skills Capability to lead by motivation and example Ability to prioritize schedule and organize Knowledge of SAS is not required, but will serve as a recommendation General knowledge of Clinical Trials and Pharmaceutical Industry Oracle/PL SQL, CDMS like OC, CT, Inform etc
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