Latest Business Insights Manager Jobs

Director, Oncology Translational Medicine Project Manager

This role leads the planning and execution of translational medicine strategies for GSK's antibody-drug conjugate (ADC) oncology portfolio. The Director drives cross-functional coordination across biomarkers, diagnostics, and clinical development, ensuring integrated project plans, governance readiness, and operational excellence. They provide strategic project management leadership, risk oversight, and insight-driven reporting to support R&D decision-making across the global oncology pipeline.

GSK Stevenage, United Kingdom

Hybrid Permanent

Director, Oncology Translational Medicine Project Manager

This role leads project management for GSK’s antibody-drug conjugate (ADC) translational medicine programs, integrating biomarker and diagnostic strategies across clinical development. The Director ensures cross-functional coordination, governance readiness, and operational execution across internal teams and external partners, driving strategic planning and compliance for key oncology R&D milestones.

GSK United States

Hybrid Permanent

Senior Global Clinical Operations Director

This role leads the operational strategy and end-to-end delivery of global clinical programs in oncology, spanning early and late-phase development. The director will drive trial design, cross-functional collaboration, and regulatory readiness while managing complex multinational studies, CRO partnerships, and high-performing teams. Emphasis is placed on innovation, efficiency, and patient impact through advanced trial methodologies and strategic leadership.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Strategy Director (Senior Consultant) – Clinical Development – Evinova

This role involves leading the development and implementation of AI and digital health strategies to transform clinical development processes. The Senior Strategy Director will act as a trusted advisor, designing digital solutions for patient recruitment, remote monitoring, and data collection while driving innovation through AI. They will lead cross-functional teams, shape operating models, and ensure digital tools are integrated into clinical protocols with a focus on measurable value and patient outcomes.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, innovative thinking, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

The Global Development Lead (GDL) in Internal Medicine is responsible for leading the clinical development of assigned assets, collaborating with cross-functional teams to design and execute clinical trials, and ensuring regulatory compliance. The role involves strategic planning, regulatory submissions, and engagement with external stakeholders to drive the clinical development program.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

This role involves leading strategic sourcing and evaluation of external innovation opportunities in Hematology and Cardiovascular/Renal therapeutic areas. Responsibilities include identifying high-potential assets, shaping early partnering strategies, and driving transactions in collaboration with Business Development. The role requires deep scientific expertise and a strong network within biotech, academia, and pharma BD organizations.

CSL

On-site Permanent

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Buyer - Pharmaceuticals

This role involves managing procurement activities, supplier relationships, and quality management within a regulated pharmaceutical manufacturing environment. You will work closely with the Manufacturing, Quality, and Operations teams to ensure effective sourcing and compliance with GMP standards.

Cranleigh Scientific Ditton, Kent, ME20 6AE, United Kingdom £22,800 – £28,800 pa

Hybrid Flexible

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. The candidate will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous improvement initiatives. It's a key position influencing patient access to medicines through robust lifecycle management.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Portfolio Innovation Director - Global Clinical Operations

This role involves leading operational innovation within global clinical trials, focusing on integrating AI-driven and technology-enabled solutions to improve trial design, patient access, and efficiency. The director will identify, evaluate, and scale innovations across the portfolio while collaborating with cross-functional teams and external partners. The position emphasizes strategic decision-making, risk assessment, and delivering measurable impact in clinical development.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Senior Medical Device Design Engineer

This role involves leading the technical aspects of medical device design and development projects, from concept to low-volume production. Responsibilities include creating 3D CAD models, supporting product testing, and working closely with manufacturing teams in a regulated environment.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Electrical Field Service Engineer

Futures are working with a leading manufacture of medical devices in their search for an Electrical Field Service Engineer. You will offer support customers across the South of England, carrying out installation, commissioning, maintenance, and fault-finding activities on specialist electrical...

Permanent Futures Limited Coventry, West Midlands (county), United Kingdom £40,000 – £45,000 pa

Refrigeration Maintenance Engineer

Refrigeration Maintenance EngineerShift: Days (Monday-Friday) + 1 Saturday per month (TOIL provided)Pay: Up to £47,000 + Premium Overtime + Excellent BenefitsLocation: Chippenham, WiltshireAre you a Refrigeration Engineer looking to escape call-out heavy contracting and join a modern environment where quality...

Yolk Recruitment Chippenham, Wiltshire, United Kingdom £44,000 – £47,000 pa

Quality & Regulatory Associate

This role involves supporting the development and maintenance of a Quality Management System aligned with ISO13485 and FDA requirements in a growing med-tech company. The candidate will manage regulatory documentation, design controls, and quality processes, contributing to audit readiness and continuous improvement. It's a hands-on position with direct impact on product compliance and regulatory submissions.

Taylorollinson Manchester, United Kingdom £35,000 – £45,000 pa

Hybrid Permanent