As a Veeva Clinical Consultant, you will be responsible for implementing, configuring, and supporting Veeva Clinical solutions to streamline clinical trial operations. You will work closely with business stakeholders, clinical teams, and technical teams to deliver high-quality solutions that meet business and regulatory requirements. Responsibilities
Configure and support Veeva Clinical applications.
Participate in study setup, configuration, and clinical trial implementation.
Gather, analyze, and document business requirements.
Support clinical operations by resolving application issues and providing functional expertise.
Collaborate with cross-functional teams to ensure successful project delivery.
Ensure compliance with GxP and industry best practices.
Assist in system testing, validation, user training, and production support.
Prepare and maintain project documentation. Qualifications
5–7 years of experience in Veeva Clinical.
Strong understanding of clinical trial processes and Life Sciences domain.
Experience with study configuration, workflows, user management, and system administration.
Excellent analytical, troubleshooting, and communication skills.
Ability to work independently and in a cooperative environment.