ELIQUENT Life Sciences
ELIQUENT Life Sciences
501 – 1,000 Employees
BiotechnologyConsultingHealthcare
ELIQUENT Life Sciences is a regulatory consulting firm serving pharmaceutical, biotechnology, medical device, and combination product companies. Its teams bring together former regulators, industry leaders, and technical specialists to guide products through development and commercialization. Work spans CMC strategy, regulatory submissions, pharmacovigilance, quality and compliance, remediation, and post-approval support, combining strategic advice with hands-on execution for market authorization and lifecycle management.

Senior Remote Pharmacovigilance Managing Consultant

Lead pharmacovigilance consulting engagements for ELIQUENT Life Sciences, overseeing client relationships, project delivery, business development, and consultant development.

Description

  • Lead consulting engagements to deliver high-quality results on time and within budget.
  • Work with client counterparts and flag when project scope or budget needs adjustment.
  • Develop clear project plans, schedules, and timelines using suitable analytical tools.
  • Coordinate work with project plans and dependencies across workstreams.
  • Lead delivery independently in small teams with limited oversight.
  • Direct complex workstreams within larger projects.
  • Ensure your own and consultants’ deliverables meet quality and timing expectations.
  • Serve as a key internal and external contact for a team or function.
  • Maintain substantial client contact at the process-owner level.
  • Plan and facilitate significant meetings.
  • Develop trusted-advisor relationships with high-value clients.
  • Identify opportunities for follow-on work and new client engagements.
  • Provide technical content for proposals, client presentations, and thought leadership.
  • Help new team members settle into ELIQUENT.
  • Manage and mentor consultants and senior consultants.
  • Improve tools and methodologies and take part in project closeout learning sessions.

Requirements

  • Bachelor’s degree in science, engineering, business, or a related discipline.
  • Typically at least seven years of relevant experience combining practical pharmacovigilance industry work and consulting or professional services experience.
  • Experience leading a workstream in a complex, multi-stream project environment with defined governance.
  • Previous leadership experience.
  • Ability to work independently or with some support, depending on client needs and the delivery model.
  • Ability to work consistently in a fast-paced, changing consulting environment.
  • Strong verbal and written communication skills.
  • Ability to understand detailed information in the context of a client’s business.
  • Ability to interpret complex issues and break them into key elements.
  • Understanding of industry regulations and how a client competes in its sector.
  • Experience creating and maintaining complex project plans and managing work against them.
  • Advanced knowledge of data-gathering methods and strong analytical ability.
  • Ability to complete all time and expense reporting promptly.

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