Clinical Project Manager Sponsor (Remote)

Our client, a global leader in biotechnology, is on a mission to transform healthcare through innovation.

Imagine being part of an international powerhouse in biotechnology that is shaping the future of medical science. Our client is not just a company; it’s a community of passionate professionals driven by a shared goal of making a real difference in the world. Here, innovation isn’t just encouraged; it’s a fundamental part of the culture.

Key Responsibilities

• Project Management: Lead interventional and non-interventional clinical studies involving medical devices and pharmaceuticals within Germany.
• Compliance & Quality: Ensure studies are conducted according to ICH-GCP guidelines, legal requirements, and both global and local SOPs, maintaining high standards of quality, time, budget, and resources.
• Coordination & Monitoring: Act as the local liaison and oversee the performance of local and global service providers.
• Documentation: Develop and contribute to study plans, materials, documents, and reports.
• Site Management: Take charge of site selection, enrollment baseline, recruitment, and other critical study activities.
• Audit Preparation: Prepare for and follow up on audits and inspections.
• Team Collaboration: Work closely with global and cross-departmental local study teams to ensure seamless project execution.

Requirements

• Educational Background: A completed degree in natural sciences or a comparable field; alternatively, completed vocational training.
• Experience: At least 7 years of professional experience in clinical research, with a minimum of 2 years as a project manager in the field.
• Regulatory Knowledge: Deep understanding and practical experience with ICH-GCP regulations.
• Vendor Management: Proven experience in collaborating with external service providers in clinical research.
• Language Skills: Fluency in both German and English, with excellent communication skills in both languages.
• Tech-Savvy: Interest in and comfort with digital communication and presentation tools.

Benefits

• Flexible Work Environment: Experience a perfect blend of modern “State of the Art” open space offices and remote work options, allowing you to thrive in a dynamic and adaptable setting.
• Continuous Learning: Take advantage of extensive opportunities for ongoing professional development to keep your skills sharp and your career on an upward trajectory.
• Financial Security: Enjoy the peace of mind that comes with comprehensive company pension schemes and other financial benefits.
• Health & Wellness: Benefit from subsidized meals and beverages, access to childcare services, and discounted rates with fitness partners to support your overall well-being.

If you’re enthusiastic about making a difference and advancing your career in clinical research, we’d love to hear from you! Please submit your meaningful application documents

Desired Skills and Experience

Clinical Development
ICH
Trial Management
Clinical Trials
Clinical Research Organizations
Clinical Monitoring
Good Clinical Practice (GCP)
Research Activities
Clinical Trial Systems

Die Personalberatung SThree betreut die ausgeschriebene Stelle im Auftrag ihres Kunden.