Project Manager – Hematology/Oncology

Posted 1hrs ago

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Job Description

Project Manager coordinating oncology/hematology clinical-trial projects for ICON, a global healthcare intelligence and clinical research organization. Managing timelines, budgets, risks, stakeholders, and cross-functional teams for pharmaceutical clients.

Responsibilities:

  • Develop and manage detailed project plans, including timelines, budgets, and resource allocation
  • Lead cross-functional project teams and coordinate efforts to meet project objectives
  • Facilitate effective communication and collaboration across project teams
  • Monitor project progress and identify potential risks and issues
  • Implement strategies to address challenges and keep projects on track
  • Engage with stakeholders to manage expectations and provide updates
  • Ensure alignment with project goals and organizational objectives
  • Prepare and present project reports, status updates, and performance metrics to senior management and stakeholders
  • Coordinate project and program management delivery, resolve issues, and develop team capability
  • Lead project delivery for large pharmaceutical clients, ensuring projects are delivered on time, within budget, and to high quality standards

Requirements:

  • Bachelor's degree in project management, business, or a related field is preferred
  • Significant project management and team leadership experience
  • Proven track record managing projects from inception to completion within scope, time, and budget constraints
  • Strong leadership and organizational skills
  • Ability to manage project teams and prioritize tasks
  • Excellent communication and interpersonal skills
  • Ability to build relationships and manage stakeholder expectations
  • Proficiency in project management tools and methodologies
  • PMP or PRINCE2 certification is advantageous
  • Detail-oriented, proactive, and adaptable
  • Commitment to achieving project goals and driving continuous improvement
  • At least 2 years of experience working for a CRO supporting Oncology/Hematology clinical trials
  • Radioligand experience highly preferred
  • Willingness to travel as required, approximately 30%
  • Legal right to work in the country where the role is based

Benefits:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways