Latest Technology Jobs

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

This role involves planning and executing studies to generate robust health outcomes data for GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure evidence supports market positioning, reimbursement, and patient access. Key responsibilities include managing study timelines, ensuring deliverable quality, and translating customer needs into study concepts.

GSK United States

On-site Permanent

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

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology drugs. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States £263,000 – £328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation priorities into portfolio planning. The position requires deep clinical expertise and a proven track record in business development and deal-making.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Senior Director, Global Clinical Program Lead, Immunoglobulin

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

SLDC Coordinator (Site Launch and Data Control) - 12-month / Secondment

This role involves managing the creation and changes of packaging for new and existing products within GSK’s supply chain, using systems like SAP, GLAMS, and CHAMPS. The coordinator ensures compliance with GMP and EHS standards while working across functions such as Quality, Regulatory, Procurement, and Logistics to maintain supply security. The position supports new product launches and pack amendments, drives process improvements, and maintains data integrity across site master records.

GSK Barnard Castle, United Kingdom

On-site Contract

Senior Engineering Technician /Secondment

This role involves providing hands-on engineering leadership to support the introduction and scale-up of new pharmaceutical products within a regulated manufacturing environment. The technician will ensure equipment and processes meet safety, compliance, and reliability standards, lead technical issue resolution, and coordinate engineering activities across teams during product launches and validation. Emphasis is placed on operational readiness, change control, and continuous improvement in a GMP-compliant setting.

GSK Barnard Castle, United Kingdom

On-site Contract

Interventional Study Scientist Director

This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.

GSK United Kingdom

On-site Permanent

Senior Director, Project Operating Model and Leadership Excellence

This position will lead the transformation of project leadership capabilities across the R&D enterprise. On a systemic level, this role will prepare critical GPL roles (Exec Directors) to be CEO of the project via a bespoke leadership/drug development/executive training and...

CSL

Quality Validation and CSV Manager

The Quality Validation and CSV Manager will lead a team responsible for ensuring all validation activities, including process, cleaning, facility, and computer systems validation, comply with regulatory requirements and GSK quality standards. The role involves managing validation protocols, collaborating with cross-functional teams, and providing technical expertise and training.

GSK Barnard Castle, United Kingdom

On-site Permanent