Latest Business Development Executive - Remote Jobs

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK £87,000 pa

Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-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 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 United States

On-site Permanent

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, United Kingdom

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 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

Junior IT Field Engineer

Junior IT Field EngineerNavan€34,000 -€40,000 Basic + Training + Technical Development + Growing Industry + Progression + Company Car + Stability + Immediate StartPassionate about IT? Do you have some experience with PC's? if so this is a fantastic opportunity...

Future Engineering Recruitment Ltd Kells, Mid And East Antrim, County Antrim, United Kingdom £29,350 – £34,529 pa

Supplier Quality Engineer - Medical Devices - Oxford

The Supplier Quality Engineer will manage and develop the supplier base for a rapidly growing medical devices company, ensuring compliance with ISO 13485 standards. Responsibilities include evaluating suppliers, managing CAPAs, and applying quality expertise to design-for-manufacture considerations.

Newton Colmore Oxford, Oxfordshire, United Kingdom

On-site Permanent

Mechanical Design Engineer

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at an exciting stage of its growth. Developing next generation wearable medical devices designed to deliver clinically meaningful physiological insights beyond the hospital environment, the business...

Cure Talent Loughborough, Leicestershire, LE11 2QG, United Kingdom £30,000 – £40,000 pa

Senior Software Engineer

This role involves developing the software ecosystem for a next-generation wearable medical device, focusing on SDKs, desktop applications, and third-party integrations. You will work closely with firmware, hardware, and data science teams to ensure robust, compliant software solutions for clinical studies and commercial deployment.

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

On-site Permanent

Senior Embedded Software Engineer - Medical Devices

This role involves designing, developing, and maintaining high-integrity embedded software for medical devices, ensuring compliance with ISO 13485 and other medical standards. The Senior Embedded Software Engineer will lead on software architecture, collaborate with cross-functional teams, and support verification and validation processes.

Verso Recruitment Milton, Cambridgeshire, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

On-site Permanent

RA Specialist

Are you an experienced regulatory professional looking for your next long-term career move?I am partnering with an innovative, medical technology business to find a dedicated Regulatory Affairs Specialist to join their growing RAQA team on a permanent & 100% remote...

GxPeople Global United Kingdom £40,000 – £50,000 pa

Production Scheduler

As a Production Scheduler, you will plan and coordinate production activities for multiple projects in a low-volume, R&D-focused medical device manufacturing environment. You will ensure efficient resource allocation, timely delivery, and compliance with ISO13485 standards, acting as a key liaison between manufacturing, supply chain, quality, and engineering teams.

Euro Projects Recruitment Shippon, Oxfordshire, United Kingdom £40,000 – £45,000 pa

On-site Permanent