Job Description

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.

• 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.