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This role involves leading the R&D Resource and Schedule Management capabilities, defining the mission, governance, and operating model. Responsibilities include capacity and demand management, scenario planning, and stakeholder engagement to ensure alignment with organizational goals and portfolio priorities.
This role involves overseeing the quality and compliance of external partners in GLP-regulated nonclinical research, including CROs and laboratories. Responsibilities include vendor qualification, risk-based monitoring, audit coordination, and ensuring adherence to regulatory standards. The role requires deep knowledge of GLP, GCP, and GMP regulations and strong cross-functional collaboration.
The Head of Operational Excellence leads process improvement activities and staff, aligning projects with business strategies. They establish and maintain performance metrics, manage operational processes, and oversee training and development of subject matter experts in a regulated, global matrix organization.
The Associate Director, Biostatistics, leads statistical contributions to clinical development programs, including study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing, and ensure the quality and timeliness of deliverables.
Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.
Leads external innovation sourcing and evaluation in Haematology, identifying preclinical to Phase 1 assets, driving due diligence, and shaping early partnering strategies. Works within the Therapeutic Area Leadership Team to advance high-potential opportunities and collaborates with Business Development to execute deals. Engages with biotech, academia, and investors to build a robust pipeline.
A little outside Edinburgh, but within reach.
The Specimen Management Associate is responsible for handling the accessioning, shipment, and storage of samples, maintaining freezer and inventory, and resolving issues. They also guide entry-level staff, respond to after-hour alarms, and ensure compliance with company procedures and regulatory requirements.
This role involves managing the security, storage, and retrieval of proprietary and client information, using scanning equipment and maintaining accurate records. The position also includes developing and implementing a sustainability strategy for IQVIA Laboratories and providing reference services to internal clients.
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