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Associate-Pharma ERP

1.00 to 3.00 Years   Bangalore   13 Jul, 2022
Job LocationBangalore
EducationNot Mentioned
SalaryNot Disclosed
IndustryIT - Software
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

    Skill required: Pharma ERP - Clinical Reports Management Designation: Associate Job Location: Bengaluru Qualifications: BE/BTech Years of Experience: 1-3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining 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 centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We 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 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 the 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 in setup activities. You will also be developing reports as per design specifications using programming languages like SQL, PLSQL, COGNOS, or SAS.In this role, you will be expected to develop clinical trial reports using SAS/ J-review / Congnos / SQL / PLSQL as per the study requirement. What are we looking for We are looking for individuals who have the following skillset:
    • Clinical Database Programming
    • Adaptable and flexible
    • Ability to perform under pressure
    • Problem-solving skills
    It would be a value add if you are proficient in:
    • SQL (Structured Query Language)
    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 teams 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.,

Keyskills :
case report formsbusiness processprofessional servicesprogramming languagesdesign specificationsclinical trialsqlerpplsqlcloudbasicformsdealspharmacognosdesignmanualchecks

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