Porta Westfalica, North Rhine-Westphalia, Germany
Passionate clinical research professional with a proven track record in orchestrating successful clinical trials and driving project excellence. My expertise lies at the intersection of: • Clinical Research & Trial Management • Project & Line Management • GCP & Regulatory Compliance • Governance & Quality Assurance • Strategic Vendor Oversight I thrive on transforming complex scientific challenges into actionable strategies, ensuring seamless execution from concept to completion. With a keen eye for detail and a commitment to ethical practices, I've successfully steered numerous trials to fruition, always keeping patient safety and data integrity at the forefront. Let's collaborate to push the boundaries of medical science and bring life-changing therapies to those who need them most. Ready to make a difference?
I am offering Services as a self-employed consultant in the area of Clinical Research and Development.
Stellv. Verantwortlicher für Arbeitssicherheit. Erstellung der Gefährdungsbeurteilung und Planung erforderlicher Maßnahmen und Trainings.
Line Management in Project Management Group. Program Oversight managing KPIs, budget, timelines and resources. Supporting business process optimisation.
Managing early phase immuno-oncology project in solid tumours.
Working closely with customers in project governance structure to manage KPIs, budget, timelines and milestones. Linie Management of PMs supporting individual growth. Providing strategic insight to Business Development activities.