Principal Project Manager

We are a leading provider of pharmacovigilance analytics software for the pharmaceutical

industry, delivering innovative, data-driven solutions that help clients enhance drug safety,

regulatory compliance, and operational efficiency.

We are seeking a Consulting Technology Project Manager to manage client implementation

projects for our Pharmacovigilance SaaS solutions. The ideal candidate will be a dynamic

client facing services professional with extensive project management experience in the life

science technology domain. This is a strategic role requiring deep project management

expertise, pharmaceutical domain knowledge, and excellent leadership skills.

This role is ideal for a highly experienced, strategic thinker with deep domain expertise in

software delivery for the pharmaceutical industry—particularly in the areas of

pharmacovigilance, safety, and regulatory technology.

Key Responsibilities :

  • Lead end-to-end project management of client software implementations, upgrades, and integrations.
  • Develop and manage project plans, including timelines, budgets, and resource demand, and author project initiation documents.
  • Coordinate cross-functional, global teams to ensure successful project delivery.
  • Serve as the primary point of contact for senior client stakeholders, ensuring clear communication and strong relationship management.
  • Ensure the accuracy, reliability, and performance of all project deliverables.
  • Monitor project progress and performance, identifying and mitigating risks and issues as they arise.
  • Facilitate regular project status meetings and provide updates to stakeholders.
  • Actively manage project scope and costs, ensuring any changes are documented and approved through formal change control processes.
  • Develop and maintain comprehensive project documentation, including project initiation documents, risk management plans, and post-project reviews.
  • Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR).
  • Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of external components or services.
  • Support continuous improvement of project management processes, tools, and best practices within the organization.
  • Mentor and guide junior project managers and team members, fostering a collaborative and high-performance team environment.

Essential Experience and Qualifications:

  • Bachelor's or Master's degree in Computer Science, Information Technology, Project Management, or a related field.
  • 8+ years of experience in project management, with at least 5 years in a senior or lead role delivering software solutions to pharmaceutical or life sciences clients.
  • Proven experience managing pharmacovigilance, clinical, or regulatory technology projects.
  • Knowledge of pharmacovigilance workflows and regulatory standards (e.g., ICH E2E, GVP Modules, FDA, EMA).
  • Expertise in project management methodologies (e.g., Agile, Scrum, Waterfall).
  • Proficiency in project management tools (e.g., Microsoft Project, Jira, SmartSheet).

Preferred Experience and Qualifications:

  • Familiarity with signal detection, case management, and safety databases (e.g., Argus, ARISg).
  • Familiarity with cloud-based solutions and big data technologies.
  • Technical background with experience in software development or IT infrastructure.
  • Knowledge of regulatory requirements and industry standards for technology solutions.
  • Certification in project management (e.g., PMP, PRINCE2).

What We Offer:

  • Competitive salary.
  • Opportunity to work with a dynamic and innovative team and world-class clients.
  • Professional development and growth opportunities.
  • A collaborative and inclusive work environment.
  • Work from home with limited travel.

Job Details

Company
Qinecsa Solutions
Location
United Kingdom, UK
Hybrid / Remote Options
Posted