*Please share the resume with **[email protected] <[email protected]>*
*Positions: Scrum Master Location: Raritan, NJ Duration: 6+ months Summary: *The Business Analyst’s (BA) will create data migration and integration plans for Regulatory, Content management, Clinical Trials, Safety and Centralized Services Integration activities. BA will be deeply involved in improving the quality, predictability and efficiency of the Information Management integration delivery capability. The BA must also ensure that the operational issues of the integrations are managed, focusing on the project interface with project leaders, stakeholders, SMEs and execution team(s) *Responsibilities:* ·Gather integration requirements and source data ·Responsible for facilitating small and medium projects from initiation to closure by working with internal (within Pfizer) and external teams ·Define and manage plans and timelines ·Manage risks and issues ·Document data mapping for integration of data for acquisition related projects ·Proactively identify project issues and collaborate with the team to develop solutions ·Perform data mapping from source to target systems ·Lead a geographically distributed team ·Ensure assigned Projects follow the Information Management integration playbook ·Manage and deploy initiatives by influence *Key Deliverables:* ·Data Transfer Plan ·Project Plan ·Communication decks ·Communication Plan ·Data collection – Product and Study data * Skills/Requirements:* ·Must possess extensive knowledge and expertise in project management, business analysis, and information integration ·Understand Clinical, Safety, Regulatory and Content Management systems and processes ·Migration Analysis and Documentation ·Bachelors or Master’s Degree ·10 years of Integration and business/industry work experience ·Minimum of 5 years of business analysis experience ·3-5 years of equivalent leadership experience ·Expertise Microsoft Office Suite (including Visio and MS-Project) *Tools and Technologies:* ·*Clinical: *EDC (e.g. Oracle Clinical), Registry (e.g. RTII), Analysis and Reporting (CDARS) ·*Regulatory: *Product and Licensing (e.g. PEARL), Submissions (e.g. eCTD) ·*Content Management: *Document Management (e.g. GDMS) ·*Safety: *Pharmacovigilance System (e.g. ARGUS) * Thanks & Regards Aman Tanwar Technical Recruiter Phone: 609-853-0818 Ext. 2171* *Fax : 609 799 5746 * *[email protected] <[email protected]>* *[email protected] <[email protected]>* *www.nityo.com <http://www.nityo.com>* -- You received this message because you are subscribed to the Google Groups "SAP BASIS" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/sap-basis. For more options, visit https://groups.google.com/d/optout.
