Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join Us as a CDM Programmer II – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our expert team, you’ll have the prospect to ensure operational excellence that makes a real difference in clinical trials. As a CDM Programmer II, you will work with clinical data management systems and programming tools to provide advanced programming support in data management activities and deliverables. This includes, but is not limited to, database development, data validations, and assisting with defining tools and techniques for improving process efficiencies. You will work within a multi-disciplinary project team to complete assigned tasks on time and within budget.
What You’ll Do:
• Performs tasks following within the timelines established by the team,
in accordance with the process outlined in the departmental procedures and indicated by the project contract.
• •Designs, builds and tests project databases & edit checks with Veeva EDC and able to work on Post production changes, handling end to end study deliverables.
• Defines and imports data into the system.
• Defines, creates and tests listings for data review and performs programming activities in line with project requirements.
• Acts as the lead on studies of simple to moderity complexity with close supervision. Researches and leverages resources to resolve issues and manage moderately complex tasks through the development and application of new knowledge and/or professional skills in areas including programming and technology.
• Participates in process improvement initiatives to increase efficiencies.
• Increases knowledge and skills to gain good understanding of the lead programmer roles and overall department processes.
• Ensures adherence to departmental