Senior Clinical Data Management Specialist

hace 4 semanas


Laza, Orense, España Associates A tiempo completo
About the Role

Veeva Systems is a leading industry cloud company, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we have surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.

At Veeva, we value our employees and prioritize their success. We offer a flexible work environment, allowing you to thrive in your ideal setting. Join us in transforming the life sciences industry, committed to making a positive impact on our customers, employees, and communities.

The Opportunity

We are seeking a skilled Consultant to join our CDMS Professional Services team. As a key member of this team, you will be at the forefront of our mission, responsible for four main areas:

  • Understanding customers' data management needs and challenges
  • Offering guidance and direction to ensure clinical trials are designed with deliverables in view
  • Implementing study designs that adhere to Good Clinical Data Management Practices and Veeva standards
  • Authoring specification documents used by team members and configuring study design during project development
Your Key Responsibilities

You will work closely with customers to review and understand clinical protocol requirements, preparing, reviewing, and finalizing all project specifications applying industry and Veeva best practices. You will also participate in Vault CDMS Product team discussions, conveying data management activities, challenges, and end-user expectations.

Additionally, you will configure forms, rules, and other study items with Veeva Vault CDMS product during development, support developers and testers during project lifecycle, and conduct on-site or remote user acceptance testing with the customer.

You will also support go-live activities for the study, ensuring a smooth transition of the study to the customer, review requirements as part of the change management process, and update specifications and configurations as necessary with associated scoping activities.

Requirements

To be successful in this role, you should possess 2+ years of experience in end-to-end data management-related activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting).

You should also have direct experience working with EDC clinical software solutions in clinical operations and/or trial management in a project management/consultant role. Life sciences industry experience and knowledge of clinical trial processes are preferred.

We are looking for an individual who can quickly understand business requirements, possess a logical approach to problem-solving, and manage multiple tasks and project deliverables. Proven track records of meeting project timelines/deliverables and attention to detail, process, deadlines, and quality results are essential.

Salary and Benefits

This role comes with a competitive salary of around $95,000 per annum, depending on location and experience. In addition, you will enjoy various benefits, including allocations for continuous learning & development, health & wellness programs, and opportunities for career growth within a dynamic organization.



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