Biotechnology Jobs

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Translates customer and payer needs into robust scientific evidence, collaborating with cross-functional teams to inform market access, reimbursement, and value-based pricing strategies. Focuses on generating high-quality, decision-ready data using diverse real-world data sources and advanced study methodologies.

GSK United States US$204,000 – US$340,000 pa

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across their lifecycle. Focuses on generating robust, scientifically credible data to inform value propositions, market access, and reimbursement strategies. Collaborates with cross-functional teams and external experts to align evidence generation with payer, clinician, and regulatory requirements.

GSK

On-site Permanent

GLP Vendor Oversight and QA Lead

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.

CSL

Senior Clinical Trial Case Manager

This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.

CSL

On-site Permanent

GLP Vendor Oversight and QA Lead

This role focuses on end-to-end quality oversight of external vendors and suppliers involved in regulated R&D activities, ensuring compliance with GLP, GCP, GMP, and GVP standards. The individual will lead vendor qualification, audit management, quality agreement negotiation, and continuous performance monitoring, while collaborating with cross-functional teams including Clinical, CMC, Safety, and Legal. A key aspect is driving compliance, data integrity (ALCOA+), and continuous improvement across third-party partners through risk-based assessments, CAPA follow-up, and QMS integration.

CSL United Kingdom

On-site Permanent