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
















