Senior Regulatory CMC Consultant Small Molecule (Veeva RIM)

Syneos Health, Inc.; Boston (MA); On-site; USD 140,000 - 200,000; Full time

Job summary

Syneos Health is seeking a Sr Regulatory CMC Consultant for Small Molecule with expertise in Veeva RIM, covering US, Canada and EMA regions from our Boston area team.

You will apply deep regulatory knowledge to maintain product readiness, prepare submissions, and advise on lifecycle management while collaborating with cross-functional teams to accelerate development and regulatory timelines.

Qualifications

• Bachelor's, Master's or PhD in a life-science field preferred.
• Typically 8 years of pharmaceutical/biotech experience or equivalent.
• Strong written and verbal communication skills essential.
• Ability to navigate regulatory requirements across NA regions.

Skills

North America regs

Regulatory surveillance

Drug development concepts

Regulatory guidelines

Communication skills

Team collaboration

Planning & prioritization

Veeva RIM

Education

Biology/Chemistry/Pharmacy/Regulatory

Tools

Veeva RIM

Job description

Syneos Health is seeking a Sr Regulatory CMC Consultant for Small Molecule with expertise in Veeva RIM, covering US, Canada and EMA regions from our Boston area team.

You will apply deep regulatory knowledge to maintain product readiness, prepare submissions, and advise on lifecycle management while collaborating with cross-functional teams to accelerate development and regulatory timelines.