Job Details

ID #50013490
State New Jersey
City Baskingridge
Job type Contract
Salary USD $1 - $60 hr 1 - 60 hr
Source Net2Source Inc.
Showed 2023-05-28
Date 2023-05-27
Deadline 2023-07-26
Category Et cetera
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Business Analyst III

New Jersey, Baskingridge, 07920 Baskingridge USA

Vacancy expired!

Description:Candidate can work 100% remote for duration of assignment.Responsibilities: Participate in the evaluation, prioritization, and implementation of system change requests Identify gaps between system capabilities and business requirements, and map capabilities to requirements to ensure that business needs are met Identify gaps between existing system capabilities and business usage Design objects, workflows, groups, permissions and other solutions to address business document management needs Revise and provide user documentation to support new capabilities or changes to existing capabilities Provide business administrative support & operational guidance to internal and external users of the relevant Clinical Systems in the R&D Domain Coordinate the translation of business and user requirements into test conditions & expected results for user acceptance testing (UAT) Develop and manage data to be utilized for UAT test cases Assist with the development and execution of change management and training throughout the organization during the implementation of system solutions Participate in the evaluation of current training practices and efforts to tailor and improve the training required to access and utilize the relevant Clinical Systems in the R&D Domain Participate in the preparation for, and discussions related to, regular Functional Administrator meetings, status meetings, change control meetings, and vendor meetings Participate in project/initiative management and contribute to defining work plans and keeping track of progressSkills:Skills Demonstrated knowledge and experience with Clinical Systems is a must Demonstrated enhancement and/or operational support experience with Clinical Trial Management Systems (CTMS) is required Relevant Pharmaceutical, Biotechnology, or Life Science industry experience is required Experience with GxP validation practices is required Experience with Regulatory Affairs / Regulatory Operations processes and systems is highly desirable Experience with Systems Development Life Cycle (analysis through implementation) practices is required Exposure to Project Management and Business Process Modeling, visualization, requirements documentation tools is required Experience with Siebel CTMS is a plus. Minimum of 3 years industry experience.

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