Latest Business Development Executive - Remote Jobs

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Global Study Lead to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK Stevenage, United Kingdom

Hybrid Permanent

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget are met. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Central Study Team to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK United Kingdom

Hybrid Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally.

Pfizer

On-site Permanent

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

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This role involves designing and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The GDL also provides expert input on trial design, regulatory activities, and external stakeholder engagement.

Pfizer

On-site Permanent

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Senior Embedded Firmware Engineer

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at a defining stage of its growth. Developing next generation optical monitoring solutions designed to deliver medical grade physiological insights beyond the hospital environment, the business...

Cure Talent Hathern, Leicestershire, LE12 5LA, United Kingdom £60,000 – £80,000 pa

On-site Permanent

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

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

Hybrid Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, Oxfordshire, United Kingdom £85,000 – £95,000 pa

Forward Deployed Engineer

This role involves leading the technical delivery of AI platform integrations for enterprise pharmaceutical customers, from initial trials to production deployment. Responsibilities include designing and implementing AI-driven integrations, collaborating with customer technical teams, and translating recurring needs into productised features within the core platform.

Harnham - Data & Analytics Recruitment London, United Kingdom £80,000 – £130,000 pa

Remote Permanent

Senior Mechanical Engineer - Biotech Mechatronics - Cambridge

Senior Mechanical Engineer - Biotech Mechatronics - CambridgeA spin-out Biotech company, based in Cambridge, is currently hiring several Senior Mechanical Engineers to join them and help accelerate the proof of concept, design, development, building, and testing of a novel life-saving...

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

Permanent

Senior Structural Enigneer

Senior Structural EngineerWarwick / up to 3 days remoteAbout the RoleYou’ll be working as part of an enthusiastic and committed team of Engineers and Technicians to deliver high quality output on projects. Client care and repeat business is crucial to...

HWA Recruitment Warwick, Warwickshire, United Kingdom £45,000 – £55,000 pa

Senior Electronic Engineer (Advert Campaign)

Senior Electronic EngineerSedgefield | Onsite role | £45,000 - £57,000About the Role:CPI is seeking a Senior Electronic Engineer to play a key role in delivering end‑to‑end product development, taking ideas from a blank page through to prototype and beyond.This is...

SRG Sedgefield, County Durham, United Kingdom £45,000 – £57,000 pa

R&D Design Engineer

The R&D Design Engineer will focus on the design, prototyping, and development of medical devices, ensuring they meet regulatory requirements and are ready for market. Responsibilities include risk analysis, process development, and introducing new technologies and materials.

Real Limerick, Limerick County, Ireland £35 – £39 ph

On-site Contract