Remote Senior Regulatory Project Manager, Strategic Lead

Veristat

Boston (MA)

Remote

USD 128,000 - 144,000

Full time

7 days ago
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Benefits offered by this job

Remote working
Flexible time off
Paid holidays
Medical insurance
Tuition reimbursement
Retirement plans

Job summary

Veristat in Boston, MA is seeking a Senior Project Manager, Regulatory Affairs to lead planning, preparation, and execution of regulatory projects across multiple therapeutic areas. You will coordinate with internal departments and sponsors, oversee timelines, ensure regulatory compliance, and integrate activities across CMC, quality, regulatory, clinical and business teams to drive successful submissions.

Strong communication, leadership, and scientific knowledge are essential to guide

Qualifications

  • Bachelor’s degree in life/health sciences or related discipline, or equivalent.
  • 6–8 years of regulatory experience in a CRO or pharmaceutical company, with ≥3 years in PM/lead role.
  • Excellent written and oral communication and strong planning/organizational skills.
  • Working knowledge of drug development and regulatory requirements, ICH guidelines.
  • Proficiency in English (written and verbal).
  • Ability to build and lead project teams and make decisions.

Responsibilities

  • Plan, prepare, and execute high-quality regulatory projects.
  • Interface with sponsors, vendors, and internal teams.
  • Coordinate across CMC, quality, regulatory, clinical and business functions.
  • Lead cross-functional project teams and manage timelines.

Skills

Regulatory experience
Project management
Leadership
Communication

Education

Bachelor's degree in life/health sciences

Job description

Veristat in Boston, MA is seeking a Senior Project Manager, Regulatory Affairs to lead planning, preparation, and execution of regulatory projects across multiple therapeutic areas. You will coordinate with internal departments and sponsors, oversee timelines, ensure regulatory compliance, and integrate activities across CMC, quality, regulatory, clinical and business teams to drive successful submissions.

Strong communication, leadership, and scientific knowledge are essential to guide

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