Job Details

ID #19889049
Estado New Jersey
Ciudad Raritan
Tipo de trabajo Contract
Salario USD Depends on Experience Depends on Experience
Fuente Kellton Tech
Showed 2021-09-19
Fecha 2021-09-16
Fecha tope 2021-11-14
Categoría Etcétera
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Clinical Business Analyst

New Jersey, Raritan, 08869 Raritan USA

Vacancy caducado!

Kellton Tech is a full-service software development company, offering end-to-end IT solutions, strategic technology consulting and product development services in Web, SMAC (Social, Mobile, Analytics, Cloud), ERP-BPM, and IoT space Our methodology of inventing infinite possibilities with technology helps us develop best in-class and cost effective solutions for our clients. My direct client is looking for Clinical Business Analyst. Below are the details of the position:

Client: Johnson & Johnson

Role: Clinical Business Analyst

Client Location:

Raritan, NJ

Duration: 12+ months contract

Summary:Business Analyst is responsible for managing and maintaining Site and Site Contact masterdata in Clinical Trial Management System (CTMS) during the study build, maintenance,and the support process. This position will also be responsible for coordinating tasks for/withteam members.

PRINCIPAL RESPONSIBILITIES:Work with Study Teams and partners during study build process to create/maintain thefollowing in CTMS:o Managing Site ID creation, maintaining the Organization/address records, maintainingContacts/Site Contacts recordso Ensuring data integrity and safeguarding against duplicate data entry in the CTMS MasterData Directoryo Supporting Study, Country, Site, Contacts, Financial Disclosure, Institution records, andPayee requestso Any other general study build activitieso Troubleshoot integration errors between CTMS and other applications• Assist with UAT activities (draft test scripts, execute test scripts, etc.)• Provide general business support for CTMS• Create/Generate reports• Run SQL queries for troubleshooting issues and general data analysis• Support Ticket generation/creation and maintenance (tracking of issues/requests)• Create/Update reference and training materials/documentation• Communicate directly with study teams to ensure issues and requests are resolved withindefined system SLA’s• Assist in any other relevant tasks required by the team

Education and Experience Requirement:University/college degree is required; preferred in health, computer science, business,engineering, or informationtechnology.2-3 years of professional experience required.Strong communicator both written and verbal is required.Experience coordinating and leading deliverables within a team is required.Prior experience with Medidata CTMS and/or Siebel CTMS or other Clinical TrialManagement systems is preferred.Prior experience working with a Master Data Management system is preferred but notrequired.Knowledge of the Clinical Trial Management process is preferred but not required.Oracle SQL experience is preferred but not required. For more information please contact Frank Williams

Vacancy caducado!

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