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Summary
This position is a member of Global Patient Safety Data Management team. The Safety Data Analyst I is responsible for performing searches in the database and generating complete and accurate reports for internal and external customers, including regulatory authorities. In addition, the Safety Data Analyst is also responsible for ensuring that information entered and retrieved from the databases is consistent and accurate and is also involved in developing and testing new report formats.
Responsibilities
The responsibilities include, but are not limited to the following:
Generate complete and accurate periodic reports and ad-hoc reports from the Pharmacovigilance database
Develop and standardize SQL queries to ensure consistency of reports generated
Collaborate with the report requestor to assure accurate interpretation of the data request
Ensure timely completion and distribution of reports and query requests
Serve as a data integrity escalation contact for downstream users of Pharmacovigilance data (Safety Writers, Drug Safety Physicians, Risk Management, Epidemiology, etc.)
Ensure consistent interpretation of system related conventions, specifications, and definitions between IT and GPS functional areas
Collaborate with Safety Systems Analysts and IT to plan and implement system related improvements regarding queries and report generation. Support may include planning, testing, piloting.
Participates in developing new report formats using Business Intelligence Tools
Take initiative to recognize, prioritize & escalate potential safety/compliance issues
Identify and troubleshoot root causes of thematic data integrity issues
Identify potential errors and omitted data found during query and address them for review to the responsible user
Interface and collaborate within the scope of these responsibilities
+ with relevant counterparts in the regional and country Pharmacovigilance functions to facilitate the global exchange of safety info
+ other functions within Pharmacovigilance in all aspects of data management
+ with other Baxter groups (e.g. Clinical and Medical Affairs, Quality, Regulatory, IT, Legal, business units, etc.).
Qualifications, education and experience
Bachelor's degree in computer science, life-science or scientific discipline or equivalent
Previous experience in performing database searches and creating reports out of a database
One year of previous experience in Safety Data Management or related area is an advantage
Understanding of Pharmacovigilance terminology is an advantage
Good knowledge of MS Excel, solid basis of SQL knowledge
Previous experience with a Business Intelligence tools (e.g. Business Objects) is an advantage
Solid understanding of database model, ideally of a Pharmacovigilance database
experience with ARISg is an advantage
Technical, analytical and problem solving skills in regards to data and queries
Strong organizational skills with strong attention to detail
Excellent written and oral communication skills
Operates effectively in a team environment
Ability to work under tight timelines
Strong organizational skills with attention to detail
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
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Job Detail
Job Id
JD3741555
Industry
Not mentioned
Total Positions
1
Job Type:
Contract
Salary:
Not mentioned
Employment Status
Permanent
Job Location
KA, IN, India
Education
Not mentioned
Experience
Year
Apply For This Job
Beware of fraud agents! do not pay money to get a job
MNCJobsIndia.com will not be responsible for any payment made to a third-party. All Terms of Use are applicable.