Pharmacovigilance Program Director — Client-Facing Leader

Eversana

Pennsylvania

On-site

USD 120,000 - 135,000

Full time

7 days ago
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Benefits offered by this job

Competitive salary with base 120k–135k
Discretionary bonuses and benefits

Job summary

EVERSANA seeks a pharmacovigilance director to oversee client programs, regulatory compliance, and delivery excellence. You will lead governance, risk management, and cross-functional teams to ensure on-time milestones and client objectives in a fast-paced PV environment.

The role requires 10+ years in PV, strong FDA/EMA knowledge, and excellent communication. Travel <15% and 40–45 weekly hours are expected within the US-based office setting.

Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related discipline.
  • 10+ years of pharmacovigilance experience.
  • 5+ years of client-facing project leadership experience.
  • Strong knowledge of FDA, EMA, ICH, and global PV regulations.
  • Experience supporting inspections and audits.
  • Experience overseeing end-to-end pharmacovigilance services.
  • Excellent communication, stakeholder management, and presentation skills.
  • Ability to manage multiple complex client programs and priorities.

Responsibilities

  • Serve as the primary point of contact for assigned clients, building trusted relationships and ensuring a high level of customer satisfaction.
  • Utilize project management principles to plan, track, and drive delivery of milestones, risks, dependencies, and action items.
  • Lead governance meetings, operational reviews, and client communications.
  • Lead governance forums, status meetings, and executive reviews, providing clear communication on project progress and key decisions.
  • Proactively identify, manage, and resolve client concerns, risks, and escalations to ensure successful project outcomes.
  • Coordinate cross-functional teams to ensure alignment, accountability, and timely execution of client commitments.
  • Provide oversight of case processing, aggregate reporting, literature surveillance, signal management, and regulatory submissions.
  • Drive development and maintenance of Safety Management Plans.
  • Drive service delivery excellence through continuous monitoring of KPIs, quality metrics, and client feedback, ensuring contractual and operational expectations are met or exceeded.
  • Ensure compliance with FDA, EMA, ICH, and client-specific requirements.
  • Support audits, inspections, CAPA management, and regulatory inquiries.
  • Monitor project financials, including billing, invoicing, resource utilization, and budget performance.

Skills

Client-facing leadership
Pharmacovigilance knowledge
FDA/EMA/ICH regulations
Audits & inspections
Stakeholder management

Education

Bachelor’s in Life Sciences/Pharmacy/Nursing

Tools

PM tools
MS Project

Job description

EVERSANA seeks a pharmacovigilance director to oversee client programs, regulatory compliance, and delivery excellence. You will lead governance, risk management, and cross-functional teams to ensure on-time milestones and client objectives in a fast-paced PV environment.

The role requires 10+ years in PV, strong FDA/EMA knowledge, and excellent communication. Travel <15% and 40–45 weekly hours are expected within the US-based office setting.

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