Job type full-time
Full job description
Skill required: clinical data management (cdm) - study build
Job location: bengaluru
Qualifications: any graduation
Years of experience: 1-3 years
Accenture is a global professional services company with leading capabilities in digital, cloud and securityCombining unmatched experience and specialized skills across more than 40 industries, we offer strategy and consulting, technology and operations services, and accenture song— all powered by the world’s largest network of advanced technology and intelligent operations centersOur 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countriesWe embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.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 patientsIt also deals with the reviewing and resolving of discrepancies identified by the system or through manual checks as per guidelinesEmployees 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 costThe team is responsible for performing data management activities including discrepancy review, query generation, and resolutionThe team is also responsible for creating crf completion guidelines (ccg) and sae reconciliation guidelinesThey 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/ecrfThe 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 anyThey also support any updates or changes to the study database (e.gProtocol amendments) through the change control processThe team participates in technical review of databases developed by other study builders, supports any updates or changes to the study (e.gProtocol amendments), conducts change control process, resolves and updates issues arising from uat including study database, ecrf, and edit checksThe 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:
Adaptable and flexible
Ability to perform under pressure
Ability to work well in a team
Commitment to quality
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.
Posted 30+ days ago