Senior Consultant - Clinical Data Programming - Remote

Overview

Veeva Systems is seeking a Senior Consultant to support life sciences companies in optimizing their use of Veeva's Clinical Data Management System (CDMS) for clinical trials, offering flexibility to work remotely or in-office.

In Short

• Act as a trusted advisor for study trial design configuration.
• Consult with customers on clinical protocol requirements.
• Drive database development activities for implementation projects.
• Collaborate with clinical data providers for data transfers.
• Configure forms and develop custom listings using SQL.
• Conduct user acceptance testing with customers.
• Support requirements gathering and go-live activities.
• Communicate risks and contingency plans with project management.
• Participate in product team discussions about data management.
• Support data ingestion into Veeva CDB.

Requirements

• 5+ years of experience with EDC clinical software solutions.
• Knowledge of clinical trial processes related to data collection.
• Experience in programming languages like SAS, R, JSON, Python, SQL.
• Expertise in life sciences industry and clinical trial processes.
• Experience in a customer-facing role.
• Ability to work independently and collaboratively.
• Excellent communication and presentation skills.
• Ability to travel up to 10%.

Benefits

• Medical, dental, vision, and basic life insurance.
• Flexible PTO and company paid holidays.
• Retirement programs.
• 1% charitable giving program.