• In this position, you will take full responsibility for managing complex clinical research projects across multiple regions. Your work will span interventional drug trials, non-interventional studies, medical-device research and technology-driven clinical initiatives. The role combines classic clinical-project oversight with hands-on coordination of the digital platforms, tools and IT services that underpin modern, patient-focused study designs

Your Benefits:

• A meaningful role contributing directly to impactful clinical research
• A supportive, team-driven work environment shaped by openness and trust
• Modern structures with flat hierarchies and no dress code
• Long-term stability with a company focused on sustainable, trust-based collaboration
• A competitive package with a permanent contract, flexible hours, generous vacation and part-remote or fully remote options depending on location
• Additional benefits including mobility programs, pension support, health incentives, learning opportunities, team events and everyday workplace perks

Your Duties:

• Act as the main contact person for the study sponsor and guide all operational steps from planning to study completion
• Drive timelines, milestones and deliverables throughout the full clinical-study lifecycle
• Oversee the project budget, track financials and update leadership regularly
• Manage the digital ecosystem used in clinical research, including platforms for data capture and patient interaction
• Translate operational requirements into actionable technical specifications for IT teams and external partners
• Ensure smooth, reliable performance of digital tools for internal teams, investigators and patients
• Work with technical specialists to resolve issues, roll out enhancements and optimize workflows
• Coordinate external partners such as CROs, technology providers and patient-service suppliers
• Develop and maintain standardized processes, documentation and operational guidelines to support compliance and consistency

Your Qualifications:

• A degree in a scientific discipline or an equivalent qualification
• Professional experience in clinical research within a CRO, biotech or pharmaceutical setting
• A proven background in managing clinical projects with digital and operational components
• Knowledge of digital or decentralized study elements and confidence using study-support platforms
• Experience with interventional studies; familiarity with non-interventional studies is an advantage
• Understanding of relevant regulatory frameworks in clinical development
• A structured, independent and solution-driven working style with strong prioritization skills
• Confidence working with digital tools, electronic data and Microsoft Office
• Strong communication abilities and a collaborative mindset

About Hays:

With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages - completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Bereitgestellt in Kooperation mit der Bundesagentur für Arbeit.