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Consultant I

Syner-G
Location
Boston, Massachusetts, United States
Posted
23 days ago
Department
Pharma Development
What they actually want (must-haves)
  • Bachelor's degree in Life Sciences, Chemistry, Biology, Engineering, Pharmaceutical Sciences, or a related scientific discipline
  • Minimum of 5 years of project management experience supporting pharmaceutical development or CMC programs
  • Experience managing cross-functional CMC development programs
  • Demonstrated experience in clinical supplies management
  • Proficiency with project management tools and software, including Microsoft Project
  • Strong understanding of pharmaceutical development and CMC activities
Nice to have
  • Advanced degree
  • Experience supporting regulatory submissions and health authority interactions
  • Experience working within consulting, fee-for-service, or multi-client environments
  • Experience with commercial supply chain operations and third-party logistics providers
  • PMP or equivalent project management certification
What the job really is

The Consultant I at Syner-G BioPharma Group will support the planning and execution of drug substance and drug product development programs, acting as the operational lead for CMC programs. This role involves managing timelines, deliverables, and risks while coordinating cross-functional activities and ensuring compliance with regulatory requirements. The position also includes responsibilities in clinical supplies management and maintaining strong client relationships.

Benefits
  • Market competitive base salary and annual incentive plan
  • Robust benefit offerings
  • Generous flexible paid time off program
  • Company-paid holidays
  • Flexible working hours
  • Fully remote work options for most positions
Things to weigh
  • Travel to client sites may be required up to 100%
  • Currently unable to sponsor or take over sponsorship of an employment Visa
Job score3/5
Benefits3/5
Freshness4/5
Career value4/5
Role clarity4/5
Pay transparency0/5

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