Senior Clinical Trial Program Lead - Remote

Veristat; Massachusetts; Hybrid; USD 130,000 - 150,000; Full time

Benefits offered by this job

Remote working

Flexible time off

Paid holidays

Medical insurance

Tuition reimbursement

Retirement plans

Job summary

Veristat, a global team with over 30 years of expertise accelerating life-changing therapies to patients worldwide, is seeking a Senior Project Manager. You will lead planning, preparation, and execution of complex clinical trial or Regulatory projects, interfacing with sponsors, vendors, and internal stakeholders.

The role requires 5–8 years of PM experience in CRO/pharma, executive communication, and a strong drug development background.

Qualifications

• Bachelor’s degree in life/health sciences or related discipline is required.
• 5 to 8 years of Project Management experience leading global/complex clinical trials in a CRO/pharmaceutical setting.
• Strong executive-level communication, written and oral, as well as interpersonal skills.
• Solid understanding of drug development and regulatory requirements (ICH, etc.).
• Proficiency in English (written and verbal).
• Ability to lead cross-functional teams and mentor/delegate.

Responsibilities

• Plan, prepare, and execute complex and high-profile clinical trial or Regulatory projects and/or programs.
• Interface with internal departments, company leadership, sponsors and vendors.

Skills

Executive communication

Planning and organization

English proficiency

Cross-functional leadership

Stakeholder management

Mentoring and delegation

Vendor/client relations

Education

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

Job description

Veristat, a global team with over 30 years of expertise accelerating life-changing therapies to patients worldwide, is seeking a Senior Project Manager. You will lead planning, preparation, and execution of complex clinical trial or Regulatory projects, interfacing with sponsors, vendors, and internal stakeholders.

The role requires 5–8 years of PM experience in CRO/pharma, executive communication, and a strong drug development background.