Veeva Clinical Operations Consult
Veeva Clinical Operations Consult
Posted on :
08-11-2024
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1 Vacancy
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Job Description
This is a remote position.
Job Title: Veeva Clinical Operations Consultant
Contract Duration: 12 months
Location: New York NY / Boston MA (Hybrid and Remote)
Job Summary:
Capgemini seeks a skilled Veeva Clinical Operations Specialist to drive the efficient management and execution of clinical trials using the Veeva Vault Clinical platform. This role involves supporting clinical study operations ensuring regulatory compliance and collaborating closely with crossfunctional teams to meet project objectives. The ideal candidate will have strong clinical operations experience and a deep understanding of Veeva applications.
Key Responsibilities:
Clinical Trial Management
- Oversee the full lifecycle of clinical trials ensuring compliance with Good Clinical Practice (GCP) and regulatory standards.
- Work with study teams to plan execute and close out trials managing study timelines budgets and resources.
Veeva Vault Clinical Platform Utilization
- Configure and manage the Veeva Vault Clinical platform to support trial operations including study setup site management and subject tracking.
- Maintain and organize all trialrelated documentation for accuracy and accessibility within Veeva.
Data Management and Reporting
- Monitor data quality within Veeva Vault ensuring data integrity and resolving discrepancies.
- Generate reports and dashboards to track trial progress site performance and recruitment metrics.
CrossFunctional Collaboration
- Work closely with Regulatory Affairs Data Management Quality Assurance and other teams to ensure smooth trial execution.
- Act as a liaison between clinical teams and external vendors for effective communication and alignment.
Training and Support
- Train clinical staff and study teams on Veeva Clinical functionalities and best practices.
- Develop user guides training materials and reference tools to enhance Veeva platform utilization.
Quality Assurance and Compliance
- Ensure adherence to company policies regulatory requirements and industry standards throughout clinical trials.
- Participate in audits and inspections providing documentation and other support as required.
Continuous Improvement
- Identify opportunities for enhancing clinical trial workflows and propose process improvements.
- Keep current with Veeva updates and industry developments to optimize platform use.
Required Qualifications:
- Handson experience with Veeva Vault Clinical and familiarity with other clinical data management systems.
- Strong clinical trial management background with an understanding of regulatory standards.
- Excellent organizational and multitasking skills with the ability to prioritize effectively.
- Strong analytical problemsolving and communication skills to work crossfunctionally.
Preferred Skills:
- Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) certification.
- Experience with additional Veeva tools and page customizations.
Why Join Us
- Work with a global leader in digital solutions and consulting.
- Contribute to innovative clinical research and operations projects.
- Enjoy a supportive diverse and collaborative work environment.
CANDIDATE SKILLS AND QUALIFICATIONS Professional experience as a data analyst, developer, or data scientist. Professional experience creating statistical or machine models to execute forecasting based on disparate and unfamiliar datasets. Coding and release experience using bash, Python, and/or other common languages. Building dashboard and reporting suites keeps stakeholders and consumers in mind through the design and iteration phases. Experience working with, analyzing, and testing deeper analytical hypothesis using utility or energy- related data sets Working within a cloud infrastructure, DevOps experience
Employment Type
Full Time
Key Skills
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