Veeva Clinical Operations- Techno- Functional Consultant
Company: Capgemini
Location: Boston
Posted on: November 15, 2024
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Job Description:
Job Description:
Check below to see if you have what is needed for this opportunity,
and if so, make an application asap.
We are looking for a dedicated Veeva Clinical Operations Specialist
to support the management and execution of clinical trials using
the Veeva Vault Clinical platform. The ideal candidate will have
experience in clinical operations, strong knowledge of clinical
trial processes, and hands-on experience with Veeva applications.
This role will involve collaborating with cross-functional teams to
ensure the successful execution of clinical studies, maintaining
compliance with regulatory requirements, and optimizing the use of
Veeva tools.
Key Responsibilities:
- Clinical Trial Management:
- Oversee the planning, execution, and closeout of clinical trials,
ensuring compliance with Good Clinical Practice (GCP) and
regulatory standards.
- Coordinate with study teams to develop and manage study
timelines, budgets, and resource allocation.
- Veeva Vault Clinical Platform Utilization:
- Configure and manage the Veeva Vault Clinical platform to support
clinical trial activities, including study setup, site management,
and subject tracking.
- Ensure that all trial-related documentation is maintained
accurately and is readily accessible within Veeva.
- Data Management and Reporting:
- Monitor data entry and ensure data integrity within Veeva Vault,
identifying and resolving discrepancies as needed.
- Generate reports and dashboards to track trial progress, site
performance, and recruitment metrics.
- Cross-Functional Collaboration:
- Collaborate with internal teams, including Regulatory Affairs,
Data Management, and Quality Assurance, to ensure seamless trial
execution.
- Act as a liaison between clinical teams and external vendors or
partners regarding clinical trial processes.
- Training and Support:
- Provide training to clinical staff and study teams on Veeva
Clinical functionalities and best practices.
- Develop training materials, user manuals, and quick reference
guides to facilitate effective use of the Veeva platform.
- Quality Assurance and Compliance:
- Ensure compliance with company policies, regulatory requirements,
and industry standards throughout the clinical trial lifecycle.
- Participate in audits and inspections, providing necessary
documentation and support.
- Continuous Improvement:
- Identify areas for process improvement within clinical trial
management and propose enhancements to workflows.
- Stay informed about Veeva platform updates and industry trends to
optimize system utilization.
Requirements:
- Proficiency in Veeva Vault Clinical and familiarity with other
clinical data management systems.
- Excellent organizational and multitasking skills, with the
ability to manage competing priorities effectively.
- Strong analytical and problem-solving abilities, with attention
to detail.
- Effective communication and interpersonal skills, with the
ability to collaborate with cross-functional teams.
- Assist the sales team as pre-sales solution architect- technical
knowledge and presentations. Understand customer requirements and
provide sales support. Conduct product demonstrations, both online
and face-to-face.
- Identify and understand the specific needs of clients. Design and
develop tailored solutions that meet client requirements. Prepare
and present proposals to clients.
- Respond to technical and functional product queries during the
sales process.
- Veeva Vault Development cloud certification (Clinical / CTMS)
Certifications:
- Clinical Research Coordinator (CRC) or Clinical Research
Associate (CRA) certification is a plus.
Job Developer
Schedule Full-time
Primary Location US-MA-Boston
Organization ERD PPL US
Keywords: Capgemini, Quincy , Veeva Clinical Operations- Techno- Functional Consultant, Healthcare , Boston, Massachusetts
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here to apply!
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