-Assist in defining requirements and designing applications to meet business process and application requirements-Perform Requirement gathering from the client for Argus implementation.-Perform the estimate’s analysis for the Argus Implementation project.-Author, dry run and formal execution of OQ scripts.-Author, dry run and coordinate formal execution of UAT PQ scripts.-Perform test scripts authoring for the RPA projects.-Assist in Argus configuration activities based on configuration baseline document through Argus Console.-Perform various activity related to validation testing.-To escalate to senior management on timely manner on any potential threats in the process.-To provide real time feedback and guidance to team members to ensure best performance.

Responsibilities as Clinical Safety Scientist:-To quality Check and Evaluate Serious Adverse Event reports in Argus safety database to ensure accurate and consistent data entry against the source documents as per the guidelines with emphasis on timelines and quality.-To ensure accurate and consistent coding of medical history, drugs and adverse events terms.-To assess adverse events report for seriousness, causality and expectedness as per applicable labelling.-To alert the Medical safety physician on potential safety issues.-Monitoring the safety profile of products, by raising attention to any potential issues or signals.Responsibilities as Medical Safety Analyst-Processing of Non-serious and Serious adverse events to ensure accurate and consistent data entry and processing from source documents, with emphasis on timeliness and quality. -Ensure accurate and consistent coding of medical history, drugs and adverse event terms. -Validate the case validity, seriousness, event term selection, coding of adverse events, suspect products, concomitant medications, lab investigations and overall consistency of information.-Assess adverse event reports for seriousness, causality and expectedness as per applicable labeling, consulting the Medical Safety Expert whenever needed and alert the Medical Safety Physicians on potential safety issues. -Writing narratives to summarize essential details of the case.-Determine the necessity for follow-up and prepare follow-up request as needed.Responsibilities as Medical Safety Associate:-As a case intake associate, responsible for duplicate search, checking of seriousness and book-in of the case.-Perform data entry of adverse events in ARGUS from Clinical trials, Solicited, Spontaneous reports, Literature and Legal cases-Identify the AE/SAE reports and prioritize the processing. Assessing priority of cases i.e. Serious/Licensee Exchange/Non serious using medical judgment.