SAP MDM Analyst Resume

SUMMARY

PROFESSIONAL EXPERIENCE
SAP MDM Analyst 5/2010 – Present
Confidential,Skillman, New Jersey

Under the Information Technology, Global Services umbrella, acquired working knowledge of Johnson & Johnson Consumer, Pharma, and Medical Devices Data in SAP, MDM.
Responsible for the creation and maintenance of the Enterprise Customer Hierarchy, in support of the GFS-I2C project.
Created new Parent Customer Numbers (PCNs) and Enterprise Customer Numbers (ECNs) in the SAP Hierarchy. Ensured all linkages/mappings are maintained and accurate for all customers.
Researched and analyzed data to ensure those customers and their global affiliates that use Johnson & Johnson products, drugs, and devices are correctly linked in the SAP database. Research accomplished by using third party vendor D&B and internet in order to assign ECNs.
Performed V-Lookups and other functions in Excel to analyze and group data for further research and validation.
Created and executed Test Scripts to support Global Class of Trade project.
Performed Customer Data Validation and edited Key Mappings for EMEA (Europe and Middle East), US, LATAM (Latin America), ASPAC (Asia and the Pacific), and CANADA, based on Regional to Global COT Mapping.
Communicated updates to Data Lead and GCDW/BW team members.
Supported month end consumer deadlines by maintaining the linkages for new and existing customers.
Aided in global clean-up efforts for customer data.
Attended weekly status meetings and represented the MDM Data platform.
Trained new hires.

Confidential,Eatontown, New Jersey

Data Manager 9/2001-12/2003

Risperidone Lead Data Manager on reformulation and phase IV studies.
Represented Data Management in weekly client and internal study meetings to report status updates.
Generated data listings and tables for review.
Fully accountable for the final condition of the clinical data for subsequent database lock.
Responsible for delegating tasks among other clinical data coordinators.
Created all edit checks according to study protocol.
Worked closely with Data Programming, Drug Safety for serious adverse reactions reconciliation, Data entry, Project Management, CRA’s, site staff, and Statisticians to support data submission time lines.
Obtained Data Management Plan approvals.
Presented at Investigator Meetings.
Worked closely with the Project Manager throughout the contract negotiation phase. Responsible for assessing hours to be utilized by Data Management. Calculated resources to adjust for complexity and priority of trials.
Trained junior coordinators on generating tables, data review, and query resolution.

Data Coordinator 9/2000-9/2001

Data Management Team member assigned to high priority studies.
Utilized manual and computer generated checks to review clinical data.
Worded queries to be sent to the site.
Utilized extensive manual data review experience to develop standards for computer generated edit checks.
Updated database upon query retrieval for data quality assurance.
All data complete and frozen ahead of schedule.

Confidential,Rahway, New Jersey

Clinical Data Analyst 9/1998-2/2000

Data Implementation Team member for phase III and IV trials for Cox II Inhibitor and Singulair Studies.
Ensured accurate case report form data entered into the Merck propriety system, paying special attention to adverse events and lab data.
Correlated lab values to clinical adverse events in the database to streamline reporting.
Performed checks to identify protocol violations for Inclusion/Exclusion criteria.
Reviewed entered data for quality control.
Made appropriate changes from queries into the database.
Generated queries from various checks programmed into the database.
Performed remote data capture user acceptance testing for newly designed data handling software. Reported updates at various project team meetings.
Worked with Laboratory Coordinators, Programmers, Physicians, in house CRA’s, and various other members of the clinical team to maintain data integrity on an ongoing basis.

Education:
Bachelor of Arts in Biology May 1998