Atos

4 weeks ago

Consultant (multiple positions available)

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 10 hours agoStatus: Live

Job Summary

Maintain clinical and regulatory affairs system applications, fix issues, configure workflows and roles, integrate vault with other systems, and manage change control. Perform system administration for GxP applications (Veeva Vault, Oracle Siebel, Salesforce, DocuSign, TVT, TMAD), validate through IQ/OQ, and translate business requirements into IT requirements while coordinating with vendors and business users. Willingness to travel and support multiple client sites across the U.S. with potential remote work.

Location: United States

Workplace: Remote

Employment Type: Full time

Job Function: Consulting & Advisory

Key Responsibilities

•Maintain clinical and regulatory affairs system application suite, fix existing issues, configure workflows, user roles, permission, document lifecycle settings, integrate vault with other systems, manage change control, document transfer, set up functions, and process information.
•Perform system administration activities for GxP applications: Veeva Vault Production Cloud Application systems (Vault eTMF/Clinical, Vault Submissions/Regulatory and Vault Quality Documents), Oracle Siebel Trial Management System, Salesforce, Content Management System, TVT (Text Verification Tool), TMAD Regulatory, DocuSign eSignature, Intelligent Editing.
•Perform test case creation including IQ/OQ to validate system functionality and document them for GxP compliance in computer system validation.
•Work with business and IT functional users on gathering requirements related to the enhancement for applications used for managing, storing, publishing, and archiving regulatory submissions and related clinical documents.
•Coordinate with product vendors on technical issues, possible solutions and enhancements.

Pay and Benefits

Salary: USD 141,336 - 142,336 annually

Key Requirements

•Bachelor’s degree in Computer Science, Information Technology, Engineering (any), or related field of study.
•Five (5) years of required Information Technology (IT) experience in Life Sciences and Pharmaceutical field.
•Five (5) years of IT experience must include: Veeva Vault; Salesforce; Oracle Siebel; ServiceNow; DocuSign eSignature; JavaScript; SharePoint; Agile / Scrum methodology.
•Experience performing IQ/OQ to validate system functionality and document for GxP compliance.
•Ability to work with business and IT users to gather requirements for enhancements to applications used for managing regulatory submissions and related clinical documents.

Experience:5+ yearsLifesciencesPharma

Education:Bachelor's

Skills:CommunicationCollaborationStakeholder management

Languages:English

Tech Stack:Veeva VaultSalesforceOracle SiebelServiceNowDocuSignJavaScriptSharePointIQ/OQAgile/ScrumTVTTMAD

Company Brief

Atos

Global digital services and consulting firm delivering cloud, cybersecurity, big data, digital workplace, and managed services to enterprise and public sector clients. Provides IT transformation, systems integration, and outsourcing solutions worldwide.

Industry: Consulting

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Bezons, France

Founded: 1997

Website LinkedIn

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Atos

4 weeks ago

Consultant (multiple positions available)

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 10 hours agoStatus: Live

Job Summary

Location: United States

Workplace: Remote

Employment Type: Full time

Job Function: Consulting & Advisory

Key Responsibilities

•Maintain clinical and regulatory affairs system application suite, fix existing issues, configure workflows, user roles, permission, document lifecycle settings, integrate vault with other systems, manage change control, document transfer, set up functions, and process information.
•Perform system administration activities for GxP applications: Veeva Vault Production Cloud Application systems (Vault eTMF/Clinical, Vault Submissions/Regulatory and Vault Quality Documents), Oracle Siebel Trial Management System, Salesforce, Content Management System, TVT (Text Verification Tool), TMAD Regulatory, DocuSign eSignature, Intelligent Editing.
•Perform test case creation including IQ/OQ to validate system functionality and document them for GxP compliance in computer system validation.
•Work with business and IT functional users on gathering requirements related to the enhancement for applications used for managing, storing, publishing, and archiving regulatory submissions and related clinical documents.
•Coordinate with product vendors on technical issues, possible solutions and enhancements.

Pay and Benefits

Salary: USD 141,336 - 142,336 annually

Key Requirements

•Bachelor’s degree in Computer Science, Information Technology, Engineering (any), or related field of study.
•Five (5) years of required Information Technology (IT) experience in Life Sciences and Pharmaceutical field.
•Five (5) years of IT experience must include: Veeva Vault; Salesforce; Oracle Siebel; ServiceNow; DocuSign eSignature; JavaScript; SharePoint; Agile / Scrum methodology.
•Experience performing IQ/OQ to validate system functionality and document for GxP compliance.
•Ability to work with business and IT users to gather requirements for enhancements to applications used for managing regulatory submissions and related clinical documents.

Experience:5+ yearsLifesciencesPharma

Education:Bachelor's

Skills:CommunicationCollaborationStakeholder management

Languages:English

Tech Stack:Veeva VaultSalesforceOracle SiebelServiceNowDocuSignJavaScriptSharePointIQ/OQAgile/ScrumTVTTMAD

Company Brief

Atos

Industry: Consulting

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Bezons, France

Founded: 1997

Website LinkedIn