English Speaking Clinical Trial Manager – Hybrid

Über das Unternehmen

Novartis is a global healthcare company based in Switzerland that provides solutions to address the evolving needs of patients worldwide. With a rich history of innovation, we are committed to reimagining medicine to improve and extend people’s lives. Our diverse portfolio includes innovative medicines, eye care, and generic pharmaceuticals. We foster an inclusive environment where our associates can thrive and contribute to our mission of finding new ways to improve and extend people’s lives.

Stellenbeschreibung

We are seeking a highly motivated and experienced English Speaking Clinical Trial Manager to join our dynamic team in Jennersdorf, Styria. In this hybrid role, you will be responsible for the end-to-end management of assigned clinical trials, ensuring their successful execution in accordance with global regulatory requirements and company SOPs. This position offers a unique opportunity to contribute to groundbreaking research and make a tangible impact on patient health within a leading global pharmaceutical company. You will lead cross-functional teams, manage external vendors, and drive operational excellence in clinical trial delivery.

Hauptverantwortlichkeiten

• Oversee the planning, implementation, and close-out of assigned clinical trials, ensuring adherence to timelines and budgets.
• Develop and manage clinical trial protocols, informed consent forms, and other essential study documents.
• Lead and motivate cross-functional study teams, fostering effective communication and collaboration.
• Select, onboard, and manage Contract Research Organizations (CROs) and other external vendors.
• Ensure compliance with ICH-GCP guidelines, local regulations, and company Standard Operating Procedures (SOPs).
• Monitor trial progress, identify risks, and implement mitigation strategies.
• Manage clinical trial budgets, resources, and timelines effectively.
• Facilitate data review, query resolution, and ensure data integrity.
• Prepare and present regular updates on trial status to stakeholders.

Erforderliche Fähigkeiten

• Bachelor's degree in a life science or related field.
• Minimum of 4 years of experience in clinical trial management within the pharmaceutical, biotechnology, or CRO industry.
• Proficiency in spoken and written English is essential.
• Strong understanding of ICH-GCP guidelines and applicable regulatory requirements.
• Proven experience in managing clinical studies from initiation to close-out.
• Excellent project management, organizational, and communication skills.
• Ability to work effectively in a hybrid environment, balancing on-site and remote work.

Bevorzugte Qualifikationen

• Master's degree or PhD in a relevant scientific discipline.
• Experience with global clinical trials.
• PMP certification or equivalent project management training.
• Familiarity with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Prior experience in oncology, immunology, or cardiovascular therapeutic areas.

Vorteile & Zusatzleistungen

• Competitive annual salary and performance-based bonuses.
• Comprehensive health and wellness programs.
• Generous paid time off and flexible work arrangements.
• Opportunities for professional development and career advancement.
• Access to innovative research and cutting-edge technology.
• Company pension scheme.
• Hybrid work model for improved work-life balance.

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