Associate – Clinical Data Management

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Job description

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Skill required: Clinical Data Management (CDM) - Study Build Designation: Associate Job Location: Chennai Qualifications: MCA,BCA,MSc Years of Experience: 1-3 years About Accenture Operations In today's business environment, growth isn't just about building value-it's fundamental to long-term business survival. So how do organizations sustain themselves? The key is a new operating model-one that's anchored around the customer and propelled by intelligence to deliver exceptional experiences across the enterprise at speed and at scale. You will deliver breakthrough business outcomes for clients-by harnessing talent, data and intelligence to revolutionize their operating models. Operations is one of four services that make up one Accenture -the others are Strategy and Consulting, Interactive and Technology. Visit us at www.accenture.com    What would you do? 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. The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects. In this role, you will work with the Study Build Team and help provide subject matter expertise in developing clinical study database by building electronic case report forms (eCRF) and program Edit Checks as per specifications in the EDC platform and perform unit testing, technical review, and fix UAT issues if any. They also support any updates or changes to the study database (e.g. Protocol amendments) through the change control process. The team participates in technical review of databases developed by other Study Builders, supports any updates or changes to the study (e.g. protocol amendments), conducts change control process, resolves and updates issues arising from UAT including study database, eCRF, and edit checks. The team is also responsible for conducting root cause analysis and coming up with preventive action. What are we looking for? We are looking for individuals who have the following skillset: Ability to establish strong client relationship Ability to manage multiple stakeholders Ability to meet deadlines Roles And Responsibilities In this role, you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your team and direct supervisor You will be provided detailed to a moderate level of instruction on daily work tasks and detailed instruction on new assignments and the decisions that you make that would impact your work You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders You will be required to help in the overall team's workload by managing your deliverables and help the team when required You will be an individual contributor as a part of a team, with a predetermined focused scope of work. Please note this role may require you to work in rotational shifts.