Senior Regulatory Affairs Project Lead (Remote)

Veristat; Massachusetts; Hybrid; USD 128,000 - 144,000; Full time

Benefits offered by this job

Remote work options

Flexible time off

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat is seeking a Senior Project Manager, Regulatory Affairs in the United States to lead planning, execution, and delivery of regulatory projects. You will collaborate with internal teams and external sponsors and vendors to integrate activities across CMC, quality, regulatory, clinical, and business areas.

The role requires 6–8 years of regulatory experience with at least 3 years in project management or team leadership, and strong English communication skills.

Qualifications

• Bachelor’s degree in life/health sciences or related discipline is required.
• 6–8 years of regulatory experience in a CRO or pharma company, with at least 3 years in project management or as a functional team lead.
• Excellent written and oral communication and interpersonal skills are required.
• Strong knowledge of drug development and regulatory requirements, including ICH guidelines.
• Proficiency in English (written and verbal).
• Action-oriented and resilient in a fast-paced environment; able to build and lead project teams.
• Ability to build trust and communicate effectively with clients, vendors, and internal teams.

Responsibilities

• Plan, prepare, and execute high-quality regulatory projects across multiple disciplines.
• Coordinate with internal departments, leadership, sponsors, and vendors to align on deliverables and timelines.

Skills

Project management

Regulatory experience

Communication skills

English proficiency

Stakeholder management

Education

Bachelor's degree in life/health sciences or related discipline

Job description

Veristat is seeking a Senior Project Manager, Regulatory Affairs in the United States to lead planning, execution, and delivery of regulatory projects. You will collaborate with internal teams and external sponsors and vendors to integrate activities across CMC, quality, regulatory, clinical, and business areas.

The role requires 6–8 years of regulatory experience with at least 3 years in project management or team leadership, and strong English communication skills.