Clinical Research Project Manager
View: 170
Update day: 16-11-2025
Location: Anderlecht Brussels Capital
Category: IT - Software IT - Hardware / Networking Information Technology Executive management Transport / Logistics / Warehouse
Industry:
Job type: Full-time
Job content
Pfizer’s Worldwide Medical and Safety colleagues play a key role in connecting evidence based medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Whether you are creating framework necessary to ensure our evidence is scientifically sound, providing unbiased, medically necessary expertise or investigating how to close gaps in data, our mission is simple. Empower healthcare decisions regarding the safe and appropriate use of medicines for patients.
What You Will Achieve
In your role, you will be joining a team that is leading Pfizer’s clinical trials and monitoring their progress. Your work helps to support all activities related to the clinical trials and supporting the teams of researchers conducting them.
As a Manager, you provide guidance to operational teams for managing projects. Your planning skills will help in preparing forecasts for resource requirements and providing areas of improvement for products, processes or services. Through your comprehensive knowledge of principles, concepts and theories of the discipline, you will also work towards advancing new concepts and methodologies. You will be able to take a leadership role to facilitate agreements between different teams.
It is your hard work and dedication that will make Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
- Provide guidance to lead/co-lead moderately complex projects.
- Responsible for site and monitoring quality, regulatory and GCP compliance.
- Drive inspection readiness and provide support for site audits/inspections as needed, following through audit/inspection finding to resolution.
- Follow the study oversight plan and proactively put in place mitigations for known/anticipated risks.
- Responsible for site and monitoring quality using and interpreting signals identified by Signal Interpretation Leads in conjunction with local country intelligence to proactively identify risks.
- Lead risk assessment at the site/country level for their studies, including identifications of mitigation and control.
- Apply knowledge of data and analytics to target site and study, recommend and implement actions for mitigation and control.
- Conduct and report oversight activities, both remote and onsite visits, according to Pfizer requirements and standards.
- Maintain ongoing relationships with senior leaders in partner lines (e.g., Legal, Corporate Compliance, Safety and Regulatory, Medicinal Sciences) to ensure appropriate quality oversight and risk management.
- Participate in and/or lead continuous process improvement projects within/between lines to increase strategic performance, enhance operating efficiencies and optimally manage operating cost.
- Use web-based technological tools for request management, i.e., tracking, workflow approvals, supply, metrics.
Qualifications
- Bachelor’s Degree (BA/BS) and 5+ years of experience.
- Excellent verbal and written communication skills in relating to stakeholders and colleagues.
- Demonstrated ability to create clear written professional communications.
- Fluent in English (C1).
Nice-to-Have
- Master’s degree (MA/MBA/MS) and 3+ years of experience.
- Strong systems and application technical skills.
- Resourcing experience preferred.
- Ability to work well and lead direct reports in a virtual. environment and in matrix and multi-cultural organization.
- French or Durch Language skills.
Deadline: 31-12-2025
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