Clinical Operations Lead m/f/d, Basel-StadtThe ideal candidate for this Clinical Operations Lead role is a patient-centric innovator with a growth mindset, driven to revolutionize clinical trial delivery. They are a collaborative leader who thrives in ambiguity, proactively managing stakeholders and inspiring diverse teams to achieve the bold vision of delivering greater patient benefit at reduced costs. This individual possesses a strong foundational knowledge of clinical operations and drug development, consistently upholding quality and compliance while fostering a culture of curiosity and continuous improvement to ensure the right treatment reaches the right patient at the right time.
Contract duration: 12 months/will be extended
Tasks & Responsibilities: - Contributing to a therapeutic area community that comprises the larger Clinical Operations Community, and enables clinical trial delivery with a focus on delivering value for patients, investigators, and clinical site staff by addressing emergent needs
- Contributing to the delivery of the PD portfolio of clinical studies and programs across Disease Areas by providing operational and/or strategic input to the teams in the Clinical Operations Disease Area Communities (CODACs).
- Drive patient-centricity (mindsets, behaviors, and actions) throughout clinical operations by always putting the needs of the patient and the investigator and clinical site staff first. Cultivate meaningful peer-to-peer collaborations to drive a deeper understanding of the patient, investigator, and clinical site staff needs across PDG and beyond. In doing so, nurture a culture of curiosity to enable faster, simpler, and more patient-centric ways of operationalizing our studies.
- Proactive stakeholder management and Alignment to achieve the Pharma Vision by collaborating influencing and partnering with many important stakeholders.
- Development, Diagnostics, Commercial, and our Affiliates as well as external Industry Collaboration Bodies, Investigators, and Clinical Site Staff, Patient Advocacy Groups, and Key Vendors.
- Promote and support quality and compliance by being accountable for GCP/GVP compliance, data integrity, and taking a balanced risk-based approach in the work you are focused on, seeking guidance or direction as needed.
Must Haves: - Science degree is required
- Minimum of 4 years working knowledge of Clinical Operations and drug development
- Knowledge of ICH Guidelines and GCP
- Knowledge of best practices and the role of Clinical Operations in pharma product development.
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