Hybrid Clinical Trial Manager – Pharma Sector

Über das Unternehmen

Bayer AG is a global enterprise with core competencies in the life science fields of health care and agriculture. Our products and services are designed to benefit people and improve their quality of life. At Bayer, we are committed to innovation, sustainability, and ethical business practices. Our Pharmaceuticals Division focuses on prescription products, especially in the areas of cardiology, oncology, gynecology, hematology, and ophthalmology, as well as radiology.

Stellenbeschreibung

We are seeking a highly motivated and experienced Hybrid Clinical Trial Manager to join our dynamic Pharmaceuticals team in Hanover. This role offers a unique opportunity to manage complex clinical trials, balancing the flexibility of remote work with essential on-site collaboration and monitoring activities. The successful candidate will be instrumental in overseeing the planning, execution, and closing of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements.

Hauptverantwortlichkeiten

• Manage and oversee all operational aspects of assigned clinical trials from study start-up through close-out.
• Develop, review, and approve study-related documents including protocols, consent forms, CRFs, and monitoring plans.
• Select, initiate, and manage clinical trial sites and investigators, including performing site visits as required.
• Monitor study progress, identify potential risks, and implement mitigation strategies.
• Manage trial budgets, timelines, and vendor relationships.
• Ensure compliance with all applicable regulations, ethical guidelines, and internal SOPs.
• Lead study team meetings and communicate effectively with internal stakeholders and external partners.
• Oversee data collection, data quality, and review of clinical trial results.
• Prepare and present trial updates to management and relevant committees.

Erforderliche Fähigkeiten

• Bachelor's degree in a life science, health-related field, or equivalent.
• Minimum of 3 years of experience in clinical trial management within the pharmaceutical or biotechnology industry.
• In-depth knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
• Proven ability to manage multiple projects simultaneously with strong organizational skills.
• Excellent written and verbal communication skills in English and German.
• Proficiency in Microsoft Office Suite and clinical trial management systems.
• Strong problem-solving and decision-making abilities.

Bevorzugte Qualifikationen

• Master's degree or PhD in a relevant scientific discipline.
• Experience in specific therapeutic areas such as Oncology, Cardiology, or Hematology.
• Demonstrated leadership experience in cross-functional teams.
• Certification in Clinical Research (e.g., CCRP).

Vorteile & Zusatzleistungen

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Generous pension scheme and retirement planning support.
• Opportunities for continuous professional development and training.
• Flexible hybrid work model.
• Employee assistance program and wellness initiatives.
• Subsidized public transport ticket.
• Company fitness and sports programs.

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