Veeva Ctms Architect

**Veeva CTMS Architect ( Job ID : 463934652 )**:

Architect
remote
Full Time

Experience

**10.0 - 14.0 years**

Offered Salary

**30.00 - 48.00**

Notice Period

**Not Disclosed**

**Experience : 10 to 14 Yrs**

**CTC-48 LPA**

**Location : Hyderabad, Bangalore & Anywhere in India**

Job Summary: We are seeking an experienced Veeva CTMS Architect to join our organization and lead the design, implementation, and management of our Clinical Trial Management System using Veeva Vault CTMS. As a Veeva CTMS Architect, you will collaborate with cross-functional teams to ensure the successful integration of Veeva Vault CTMS capabilities, ensuring compliance with regulatory requirements and efficient management of clinical trial operations. Your expertise in Veeva CTMS and your understanding of clinical trial processes will be critical in driving streamlined and compliant trial management.

**Responsibilities**:

- Design and architect the Veeva Vault CTMS system to meet regulatory compliance and streamline clinical trial management processes.
- Collaborate with stakeholders to gather requirements and translate them into system configurations and enhancements.
- Customize Veeva Vault CTMS modules and workflows to align with clinical trial processes and regulatory standards.
- Conduct system assessments, identify gaps, and propose solutions to enhance system performance and compliance.
- Develop and maintain system documentation, including user guides, configuration guides, and SOPs.
- Provide technical expertise and guidance to the implementation team, ensuring best practices and efficient use of the Veeva Vault CTMS system.
- Collaborate with IT teams to integrate Veeva Vault CTMS with other enterprise systems, such as EDC (Electronic Data Capture) or eTMF (electronic Trial Master File).
- Stay up to date with industry trends, new features, and updates related to Veeva Vault CTMS, and assess their applicability to the organization.
- Assist in user training and provide ongoing support to end-users, addressing system-related inquiries and issues.
- Ensure compliance with regulatory standards, such as ICH-GCP (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use - Good Clinical Practice) and 21 CFR Part 11.

**Required Knowledge, Skills, and Abilities**:

- Architect