Overview

Syneos - Clinical and Corporate - Prod is seeking a Regulatory Consultant CMC for small molecules, responsible for managing regulatory activities through the product lifecycle. The idóneo candidate will have expertise in CMC and Veeva Vault RIM, and the position requires Eastern Standard Time availability.

Responsibilities

• Conduct research and manage regulatory submissions to support product development and lifecycle management.
• Collaborate with multidisciplinary teams to ensure regulatory compliance and successful project delivery.

Qualifications

• Experience in regulatory affairs for small molecules with a focus on CMC.
• Expertise in Veeva Vault RIM is preferred.
• Availability in Eastern Time (EST).