You will be aligned with our Pharmaceuticals Processes vertical and help us with the processes to collect, monitor, research, assess and evaluate information on the adverse effects of medication with a view to identifying new information about hazards associated with medicines and consequently, prevent harm to patients. It also deals with the reviewing and resolving of discrepancies identified by the system or through manual checks as per guidelines. Employees under this span can also be responsible for a number of activities related to the design, development, and maintenance of Clinical Database objects.
You will be working as a part of Pharma ERP team which is responsible for a number of activities related to the design, development, and maintenance of clinical database objects. Maintenance of case report forms, database objects, forms, edit checks and procedures. Will develop Study Data Tabulation Model (SDTM)) solutions and work on the end to end ma in setup activities. Develop reports as per design specifications using programming languages like SQL, PLSQL, COGNOS or SAS.
In Pharma Elec Data Capture (EDC), You will be responsible for designing, developing and delivering business solutions related to the computerized systems used for the collection of clinical data in electronic format for use mainly in human clinical trials.
Good to have skills: Good communication skills,Analytic skills,Computer/Technological Skills
Roles and Responsibilities
In this role you are required to do analysis and solving of lower-complexity problems. Interaction is with peers within Accenture before updating supervisors. Likely has limited exposure with clients and/or Accenture management. Moderate level instruction on daily work tasks and detailed instructions on new assignments would be provided. Decisions impact own work and may impact the work of others . Individual contributor as a part of a team, with a focused scope of work. Please note that this role may require you to work in rotational shifts.