Clinical Data Management Specialist

hace 2 días


Barcelona, Barcelona, España Veeva Systems A tiempo completo
About the Role

Veeva Systems is a pioneering organization in industry cloud, driving innovation to help life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we achieved $2 billion in revenue in our last fiscal year with vast growth potential ahead.

Our core values at Veeva are centered around Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history by becoming a public benefit corporation (PBC) in 2021, legally bound to balancing the interests of customers, employees, society, and investors.

We offer a flexible work environment as a Work Anywhere company, supporting your choice to work from home or in the office, so you can thrive in your ideal setting.

The Opportunity

Veeva Vault Clinical Data Management System (CDMS) is revolutionizing clinical data management in the industry. By combining EDC, coding, data cleaning, and reporting into one application, research teams can make faster and more informed decisions.

We're seeking experienced Consultants who have expertise in life sciences software configuration, specifically in helping customers optimize the use of EDC in running their clinical trials. The ideal candidate will have experience in EDC design and configuration, as well as a working understanding of data management, cleaning, and reporting.

As a key member of our CDMS Professional Services team, you'll be responsible for four main areas:

  • Understanding customers' data management needs and challenges
  • Offering guidance and direction to ensure that the clinical trial is designed with deliverables in mind
  • Implementing study designs in the Vault CDMS application adhering to Good Clinical Data Management Practices and Veeva standards
  • Configuring forms, rules, and study items during the development phase of the project
Responsibilities

You'll work closely with customers to review and understand clinical protocol requirements, prepare project specifications applying industry and Veeva best practices, and participate in Vault CDMS Product team discussions to convey data management activities and end-user expectations.

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

In addition, you'll ensure customer success from beginning to end of the project life cycle, assure process compliance with all regulatory and Veeva procedural requirements, and participate in initiatives to improve processes, products, and best practices.

Requirements

To succeed in this role, you'll need:

  • At least 2 years of experience in end-to-end data management-related activities (database design, data collection, data analysis, query resolution, datasets, statistical reporting)
  • 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 preferred (pharmaceutical, biotech, medical device companies, CRO's, and academic & public health organizations)
  • Experience in a customer-facing role, preferably with a software professional services organization or consulting background
Benefits

Veeva offers an estimated salary range of $80,000-$120,000 per year, depending on location and experience. Our benefits package includes allocations for continuous learning and development, health and wellness programs, and a flexible work environment. If you're passionate about life sciences and committed to making a positive impact, apply today



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