Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have (EMEA /US/Ca

About the role

Syneos Health is a life sciences services organization supporting drug development and commercialization. This role owns regulatory CMC activities for small molecules and Veeva RIM expertise in a global context, focusing on EMEA, US, and Canada regulatory frameworks.

What you'll do

• Apply knowledge of North America regulatory affairs to maintain products on the market and manage reporting and surveillance.
• Interpret regulatory guidelines and contribute to regulatory strategy for small molecule products.
• Collaborate with teams to plan and prioritize work effectively within projects.
• Communicate clearly in written and verbal form to internal and external stakeholders.
• Utilize Veeva RIM systems and related tools to support regulatory information management.
• Provide regulatory support across a global delivery environment as needed.

What they're looking for

• Strong knowledge of North America regulatory affairs framework.
• Experience with regulatory processes to maintain market status, reporting, and surveillance.
• Understanding of drug development concepts and related regulatory requirements.
• Ability to assess guidelines and communicate findings effectively.
• Experience with Veeva RIM or similar regulatory information management systems.
• Bachelor’s or higher degree in life sciences or regulatory related field with substantial experience.

For applicants in Nigeria

• The listing includes a broad remote location spanning many countries; it does not state explicit timezone or country restrictions for Nigeria. Confirm before interviewing.
• Remote work eligibility is indicated; no explicit on-site location required in the listing.
• Pay currency or range is not specified in the listing; confirm during interview process.
• No visa or work-authorization specifics for Nigeria are stated; confirm eligibility with the employer.