
Project Manager II, Oncology
Posted 2 days ago

Posted 2 days ago
This is a fully remote position, open to applicants in Netherlands.
• Supervise and direct oncology projects on a domestic, regional, and/or global scale, occasionally under the guidance of a Project Director.
• Develop and oversee project teams, manage communications, assess risks, define scope, schedule, costs, quality, and stakeholder engagement.
• Proactively address project variances and ensure client expectations are fulfilled.
• Utilize a comprehensive understanding of drug development and the execution of clinical trials.
• Compile and manage project documentation, ensuring the accuracy and quality of regulatory data.
• Act as a primary point of contact for clients, fostering strong relationships with client project teams.
• Lead core project teams and promote collaboration among internal and external stakeholders.
• Raise project issues to the relevant internal and external parties.
• Identify and resolve conflicts in a proactive manner.
• Grasp project delivery strategies, cost assumptions, and budget considerations.
• Deliver projects according to agreed-upon scope, schedule, costs, quality, contractual obligations, and financial performance targets.
• Manage both internal and external change control processes.
• Lead quality control and risk assurance initiatives.
• Create, manage, review, and adjust project plans and variances in compliance with SOPs.
• Ensure that assigned staff adhere to professional standards and SOPs, providing feedback on performance.
• Develop and sustain project performance indicators and client-specified KPIs.
• Determine project resource requirements and succession planning.
• Prepare and present new business proposals in collaboration with pertinent departments.
• Train and mentor PM Academy Project Coordinators.
• Potentially oversee line-management and talent development activities, including onboarding, development, retention, competency assessments, and performance reviews.
• Provide line management and technical support to designated project leaders.
• Undertake additional duties as assigned.
• A university or college degree (preferably in life sciences) or certification in a related allied health profession (e.g., nursing, medical or laboratory technology) from an accredited institution.
• Fortrea may consider equivalent relevant experience in lieu of educational qualifications.
• A minimum of seven (7) years of pertinent clinical research experience in a pharmaceutical company or CRO, including at least two (2) years with full project management responsibilities.
• Strong experience in Oncology.
• Working knowledge of ICH Guidelines and GCP, along with international regulatory requirements for conducting clinical development programs.
• Proficient in advanced computer skills, including Microsoft Word, Excel, Project, Access, and PowerPoint.
• Experience in managing projects within a matrix and virtual environment.
• Excellent skills in communication, planning, and organization.
• Proven ability to lead by example and encourage team members to independently seek solutions.
• Proven capacity to manage multiple competing priorities and effectively utilize resources.
• Demonstrated ability to inspire teamwork and motivate staff in a matrix environment.
• Financial acumen and the ability to effectively use financial tracking systems.
• Solid understanding of project management processes.
• Capability to work independently and mentor junior project team members.
• Proficiency in negotiating and liaising with clients in a professional manner.
• Ability to present to staff across all levels.
• Preferred: Master’s or other advanced degree.
• Preferred: PMP certification.
• Preferred: Experience in the biotech field.
• No specific benefits or compensation extras stated in the posting.
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