Clinical Data Programming Specialist

6 days ago


Étreux, Hauts-de-France, United States Veeva Systems Full time
About Veeva Systems

Veeva Systems is a pioneering organization in the industry cloud, dedicated to helping life sciences companies bring innovative therapies to patients faster. With an impressive track record of growth, we surpassed $2 billion in revenue in our last fiscal year, with significant potential for expansion ahead.

At the heart of Veeva are our core values: Doing the Right Thing, Customer Success, Employee Success, and Speed. As a public benefit corporation (PBC), we're committed to balancing the interests of customers, employees, society, and investors.

We offer a flexible Work Anywhere environment, allowing you to thrive in your ideal work setting – whether that's from home or in the office.

Join us in shaping the future of the life sciences industry, dedicated to making a positive impact on our customers, employees, and communities.

The Role

Veeva seeks an experienced Clinical Data Programmer to support internal and customer teams in configuring Veeva CDB. This hands-on programming role plays a critical part in providing consultation and guidance to customers on best practices for implementing Veeva CDB. You'll collaborate closely with the customer data management team and Veeva CDB Project Manager to ensure successful implementation and adoption of Veeva CDB, while contributing to its evolution and improvement.

Veeva Clinical Database (CDB) is a next-generation clinical data platform that centralizes and automates data imports, cleaning, and management for clinical trials. Designed to scale and accommodate all relevant data for a trial, this innovative advancement aims to speed up the process of getting new treatments to market.

Key Responsibilities
  • Develop custom listings based on customer data cleaning requirements using SQL-based language
  • Configure and support data ingestions (imports) into Veeva CDB
  • Collaborate with clinical data providers (Central Laboratories, ECG, eCOA, IRT, etc.) to receive data and test the transfer based on requirements
  • Provide mentoring to customer programming / configuration teams
  • Discuss Veeva CDB best practices with customer teams, leveraging industry knowledge regarding Clinical Data Programming
Requirements
  • 5+ years of experience in Clinical Data Programming (EDC Development, SAS, SDTM, etc.)
  • Prior experience in programming languages such as (SAS, R, JSON, Python, SQL) with the ability to learn new programming languages (SQL based language)
  • Working knowledge of clinical trial processes specifically as they relate to data collection and review
  • Proven ability to manage diverse stakeholders, and ensure delivery to a high degree of satisfaction
  • Proven ability to work independently in a dynamic, fast-moving environment, but also as part of a team where you need to 'roll up your sleeves' to implement a clinical solution
  • Ability to travel up to 25%
Compensation

The estimated annual salary for this role is between $80,000 - $200,000, depending on experience and qualifications. We consider individual circumstances when determining compensation, aiming to recognize unique contributions and qualifications. In addition to base pay, other types of compensation may be available, including variable bonus and/or stock bonus.



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