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Veeva CTMS Specialist at Remote, Remote, USA
Email: [email protected]
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=421289&uid=

Hello,

Title: Veeva CTMS Specialist

Location: Remote

Duration: Long Term

Visa: Independents only

Description:

Configure and customize Veeva Vault CTMS modules and workflows to align with clinical trial processes and business needs.

Collaborate with stakeholders to gather requirements and translate them into system configurations and enhancements.

Conduct system assessments, identify gaps, and propose solutions to enhance system performance and compliance.

Provide end-user support, troubleshooting, and issue resolution related to Veeva Vault CTMS functionality.

Assist in the implementation of new features and upgrades within Veeva Vault CTMS.

Collaborate with cross-functional teams, including clinical operations, data management, and IT, to ensure seamless integration and data integrity with other clinical trial systems.

Collaborate with vendors and external partners to ensure effective utilization and interoperability of Veeva Vault CTMS.

Develop and maintain system documentation, including user guides, configuration guides, and SOPs.

Stay up-to-date with Veeva Vault CTMS platform updates, new features, and industry best practices, and apply them to enhance system capabilities.

Provide user training and educational sessions to ensure effective utilization of Veeva Vault CTMS.

Qualifications:

Bachelor's degree in Life Sciences, Computer Science, Information Systems, or a related field.

5+ years of experience working with Veeva Vault CTMS or similar clinical trial management systems.

Strong understanding of clinical trial processes, including study startup, site management, and trial monitoring.

Experience in configuring and customizing Veeva Vault CTMS modules, workflows, and reports.

Familiarity with regulatory requirements and guidelines such as ICH-GCP (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use - Good Clinical Practice).

Excellent problem-solving and analytical skills, with the ability to troubleshoot system-related issues.

Strong communication and interpersonal skills to effectively collaborate with cross-functional teams and external stakeholders.

Familiarity with data integration and system interoperability within the clinical trial ecosystem.

Knowledge of other clinical trial systems such as EDC (Electronic Data Capture) or eTMF (electronic Trial Master File) is a plus.

Veeva Vault CTMS certification is highly desirable.

Thanks & Regards,

Archie,

CII DIVERSITIES LLC, 

(Subsidiary of Comspark International)

"IT'S synergy par excellence"

SAP Partner | Minority Certified | ISO 9001-2008 Certified

Outsourcing | Application & Product Development |Analytics I Digital

& Staff Augmentation.

Off :

901-414-9940

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Keywords: information technology
http://bit.ly/4ey8w48
https://jobs.nvoids.com/job_details.jsp?id=421289&uid=
[email protected]
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11:56 PM 18-Jul-23


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