Remote Senior Regulatory Project Manager

Veristat, LLC; United States; Remote; USD 128,000 - 144,000; Full time

Benefits offered by this job

Remote working

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat, LLC is seeking a Senior Project Manager, Regulatory Affairs to lead and coordinate regulatory projects across CMC, quality, regulatory, clinical and business domains. You will interface with sponsors, vendors, and internal leadership to ensure timely, compliant delivery of high-quality programs.

The role requires 6–8 years in regulatory affairs within a CRO or pharmaceutical setting, plus at least 3 years in project management or team leadership.

Qualifications

• Bachelor’s degree in life/health sciences or related discipline or equivalent required.
• 6 to 8 years of relevant Regulatory experience in a CRO/Pharma company with at least 3 years in Project Management or lead roles.
• Excellent written and oral communication and interpersonal skills; strong planning and organizational ability.

Responsibilities

• Plan, prepare and execute high-quality regulatory projects.
• Interface with internal departments and company leadership, and externally with sponsors and vendors.
• Integrate consulting activities across CMC, quality, regulatory, clinical and business in coordination with other teams.
• Lead and motivate project teams, delegate tasks, and drive decisions to deliver on milestones.

Skills

Project management

Regulatory affairs

Clinical research

Life sciences

Communication skills

Education

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

Job description

Veristat, LLC is seeking a Senior Project Manager, Regulatory Affairs to lead and coordinate regulatory projects across CMC, quality, regulatory, clinical and business domains. You will interface with sponsors, vendors, and internal leadership to ensure timely, compliant delivery of high-quality programs.

The role requires 6–8 years in regulatory affairs within a CRO or pharmaceutical setting, plus at least 3 years in project management or team leadership.