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Listed below are the top 10 out of 28 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Round Lake, IL


 
 

Mar 28

Baxter International, Inc - Vernon Hills, IL US

Vernon Hills, IL Req ID 50803BR Business Title Safety Systems Analyst II Business Global Quality SubBusiness Global Pharmacovigilance Country US State/Province ...

Apr 15

Baxter International, Inc - Deerfield, IL US

Deerfield, IL Req ID 52474BR Business Title Safety Data Analyst II Team Lead Business Global Quality SubBusiness Global Pharmacovigilance Country US State/Province ...

May 14

Randstad Pharma - Chicago North, IL US

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May 16

Kraft Foods - Chicago, IL US

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May 17

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May 19

Abbott Laboratories - Chicago, IL US

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May 25

Icon Clinical Research - Chicago, IL US

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May 24

MedFocus Pharmaceutical Research Opportunities - Chicago, IL US

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May 18

Confidential - Chicago, IL US

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May 26

Green Key Resources LLC - Chicago North, IL US

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To view more listings click here to search Science Jobs in Round Lake, IL


For your reference, we have included the original job posting below.




Quality Data Analyst II


Job Number:41653546
Company Name:Baxter International, Inc
Job Location:Round Lake, IL US
Job Categories:Science & Biotech
Engineering & Architecture


Quality Data Analyst II

Round Lake, IL

Req ID 50812BR

Business Title
Quality Data Analyst II

Business
Global Quality

Sub-Business
Global Field Surveillance

Country
US

State/Province
Illinois

Location of Position
Round Lake, IL

Shift_
1st

Job Description
This position is a senior member of the Global Field Surveillance (GFS) Data Analyst Team. The Quality Data Analyst II provides direct technical / data management and oversight of the complaint reporting systems to ensure information retrieved from the system is consistent, accurate and complete. The Quality Data Analyst II is a technical expert in GFS for data management, reports and queries.
Responsibilities:

•Develop system ad-hoc reporting tools to facilitate end user complaint reporting

•Lead/coordinate/participate in reports management tasks/projects requiring technical expertise with respect to GFS complaint systems

•Ensure periodic and ad-hoc reports generated are complete and accurate

•Drive the standardization of queries to ensure consistency of reports generated

•Foster collaboration with the report requester to assure accurate interpretation of the data request

•Ensure timely completion and distribution of report requests

•Train GFS team members on complaint system queries and other database related tasks in close collaboration with GIT

•Coordinate requests to GIT for complaint reporting system database issues regarding queries and report generation that require GIT intervention and support including those under change control

•Perform user acceptance testing of system changes implemented by GIT in relation to data queries and report generation

•Assist with the development of reports management related processes and SOPs.

•Interface and collaborate within the scope of the following:

•with relevant counterparts in the regional and country Product Surveillance functions to facilitate global exchange of complaint related information.

•Other functions within GFS in all aspects of data management

•With other Baxter groups (e.g. Clinical/Medical Affairs, Quality, Regulatory, IT, Legal, business units, etc.)

•Gather requirements from Global Business Units to provide meaningful, actionable trending data both internally and externally

•Determine the appropriate source for the data and use the required tools

•Evaluate findings and present in an actionable format to management.

•Represent GFS Data Analysis Team on CAPA investigations

Job Requirements

Qualifications:

•Excellent technical, analytical and problem solving skills as it pertain to complaint data management

•Strong understanding of data structure of complaint database

•Ability to lead project teams

•Ability to develop and train others

•Excellent oral and written communication skills

•Excellent interpersonal skills that encourage teamwork

•Advanced knowledge of complaint terminology

•Excellent attention to detail

•Broad knowledge of FDA regulations

•Provide guidance to internal project teams in the area of design and analysis of reports for routine projects

•Oversee the preparation, planning, coordination, execution, confirmation and ongoing maintenance of complaint reports Provide technical review of reports/report related documents to be presented both inside and outside of Baxter Education and Experience:

•BA/BS + 2 years experience or equivalent Preferred Qualifications:

•Bachelor degree in scientific discipline, life, or computer science or equivalent

•Experience as both an individual contributor and as a participant/leader in a team environment.

•2+ years of previous experience in complaint data management in the Pharmaceutical, Device or Biotech industries (Sponsor, CRO or combination) in roles of increasing responsibility

•Possess strong analytical and problem solving skills

•Effectively interact and communicate with cross-functional team members

•Ability to work independently with an appreciable degree of latitude and ability to keep up with changing priorities and requests

•Detail oriented, thorough, and well organized

•Demonstrate the ability to learn diverse business applications and master new software quickly

Doing Work that Matters
Baxter provides its employees with comprehensive compensation and benefits. To view additional opportunities at Baxter and to learn more about the company, please visit our Web site at company website. EOE M/F/D/V.

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