Project Manager
EORTC - European Organisation for Research and Treatment of CancerBelgium1 day ago
Full-timeProject Management, Information Technology
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Projects and Services is looking for one Project Manager (PM) to reinforce its team.
The Project Manager works under the hierarchical supervision of the Projects Director.
Objective
The Project Manager (PM) is responsible for planning, monitoring and controlling multiple oncology clinical trials and/or research projects, from project initiation to completion. The PM ensures that project objectives are achieved and oversees trials to ensure they are conducted ethically, efficiently, with a strong focus on patient safety and data integrity.
The PM leads the project team functionally and manages communication with internal stakeholders (e.g. Project team members, other PMs, Heads of departments) and external stakeholders (e.g. upstream partners, vendors, intergroups, study coordinators).
Main responsibilities / Major Activities
Education & Experience
The Project Manager works under the hierarchical supervision of the Projects Director.
Objective
The Project Manager (PM) is responsible for planning, monitoring and controlling multiple oncology clinical trials and/or research projects, from project initiation to completion. The PM ensures that project objectives are achieved and oversees trials to ensure they are conducted ethically, efficiently, with a strong focus on patient safety and data integrity.
The PM leads the project team functionally and manages communication with internal stakeholders (e.g. Project team members, other PMs, Heads of departments) and external stakeholders (e.g. upstream partners, vendors, intergroups, study coordinators).
Main responsibilities / Major Activities
- Trial planning and set-up Manage multiple clinical trials and research projects, ensuring all activities and deliverables are clearly defined, scheduled, and meet budget and quality targets. Develop comprehensive project management plans, detailing tasks and responsibilities, schedules, and budget.
- Trial execution &oversight Oversee project execution to ensure deliverables are completed on time, within budget, and to the expected quality. Monitor progress and proactively address deviations or risks
- Stakeholder management Manages project’s external stakeholders including communication, contractual commitments and budget. Serve as the project primary point of contact for Upstream partners.
- Team Leadership Leads, motivates, and coordinates the project team ensuring effective transversal coordination. Collaborate with Department heads to secure adequate project staffing.
- Quality & Compliance Ensure adherence to ICH GCP E6(R3) and EORTC policies and procedures Ensure high-quality documentation in CTMS and eTMF systems Prepare for and support audits and inspections Contributes to improving project management processes within Projects Direction
- Risk Management Integrate risk-based quality management and Quality-by-Design principles throughout the project lifecycle Facilitate risk identification, assessment and management within the study team
- Change Management Anticipate project’s changes with internal and external stakeholders.
- Internal communication Maintain clear communication and alignment with internal stakeholders, including reporting and escalation of issues when needed.
- Mentorship Provides guidance and mentorship to newcomers.
- Develop study budget and timelines during the study initiation phase
- Document study management, communication, risk and TMF management in study plans
- Engage with upstream partners (e.g. industry partners, grant providers)
- Oversee contract set-up with providers and collaborating groups
- Coordinate study team activities from initiation to study close-out, including
- Leading project-based meetings and risk review sessions,
- Overseeing study team training
- Monitor project deliverables, budget, timelines, quality, risks and change requests
- Report progress using Dynamics and other management tools
- Manage trial close out activities and ensure proper documentation archiving
Education & Experience
- Minimum education requirement: master’s degree in sciences, pharmacy or management.
- Minimum 5 to 7 years’ experience in a project management in highly scientific environment or in operations role in the field of clinical trials.
- Solid understanding of ICH GCP E6(R3), and clinical trial regulation
- Experience with CTMS, eTMF, and EDC systems,
- knowledge of Project Management areas (PMI), PMP certification is a plus
- Fluency in English (spoken, written) is required.
- Team player with strong leadership skills, using open communication and influencing skills to work effectively within teams and across functions
- Financial acumen, understanding financial principles for budgeting and forecasting.
- Open minded profile, with strong desire to learn and with the ability to work in a multilingual and multicultural environment.
- Strong negotiation skills are a plus for contract management and external stakeholders’ management.
Key Skills
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