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 ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.

GSK

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.

GSK Stevenage, 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 approvals and global market access. The role also includes specialized monitoring, regulatory submissions, and engaging with external stakeholders to drive strategic insights.

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, working closely with cross-functional teams to design, execute, and interpret clinical studies. Key responsibilities include creating clinical development plans, regulatory submissions, and providing expert input on trial design and execution, while ensuring compliance and strategic insight generation.

Pfizer

On-site Permanent

Associate Director Clinical Supply IRT

This role involves leading the onboarding and continuous improvement of IRT standards and studies for AstraZeneca's clinical trials. Responsibilities include technical documentation, risk assessment, test script development, training, and process optimization. The position requires deep knowledge of R&D supply chain, clinical development processes, and IRT systems, with a focus on delivering high-quality, efficient clinical trial supplies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Director, Statistical Programming

This role involves leading and developing a team of programmers, providing strategic direction for statistical programming in clinical development, and ensuring quality, compliance, and continuous improvement. The Director will partner cross-functionally to drive business impact and maintain industry and regulatory knowledge.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Field Service Engineer

Field Service EngineerBirmingham£35,000 - £48,000 Basic + Training + Progression + Van + Work-Life Balance + Stability + Regional Patch + Immediate StartAre you a Field Service Engineer looking to build a long-term career with a rapidly growing young medical...

Future Engineering Recruitment Ltd Birmingham, West Midlands (county), United Kingdom £35,000 – £48,000 pa

Field Service Engineer

Field Service EngineerLondon£35,000 - £48,000 Basic + Training + Progression + Van + Work-Life Balance + Stability + Regional Patch + Immediate StartAre you a Field Service Engineer looking to build a long-term career with a rapidly growing young medical...

Future Engineering Recruitment Ltd London, United Kingdom £35,000 – £48,000 pa

Formulation and Application Specialist

Exciting Opportunity: Formulation & Application SpecialistAre you a hands‑on formulation scientist who enjoys seeing products progress from concept through to manufacture? This organisation is seeking a Formulation & Application Specialist to join its R&D function, playing a key role in...

SRG Halifax, West Yorkshire, HX1 1TH, United Kingdom

On-site Permanent

Chemical Process Operator

This role involves operating chemical process plant and manufacturing equipment, following batch manufacturing instructions, monitoring chemical reactions, and supporting material handling and packaging activities. The position offers long-term stability and development opportunities within a safety and quality-driven manufacturing environment.

Talent STEM Ltd Stradishall, United Kingdom

On-site Permanent Shift-work

Cyber Security Architect - Genomics, Data, Insurance

Cyber Security Architect - Genomics, Data, Insurance£Market Rate - Inside IR35London / Hybrid3 months initiallyMy client is an instantly recognisable Insurer who require a hands-on Cyber Security Architect with deep expertise in securing highly confidential data to support the design...

Hays Technology London, City And County Of the City Of London, United Kingdom

Regulatory Affairs Assistant

Regulatory Affairs Assistant – Devon – Up to £30,000 + Benefits – REF 065£25,000 pa - £30,000 pa + Company Bonus + BenefitsDevonMon – Fri40 hours p/wAn exciting opportunity has arisen to join a global manufacturing organisation that develops, manufactures,...

L-ev8 Recruitment Ltd Plymouth, Devon, United Kingdom £25,000 – £30,000 pa

On-site Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Lead Patent Paralegal

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Disease Level Partner - South Central UK

The Disease Level Partner (DLP) is responsible for implementing Roche's strategy and objectives within therapy areas, focusing on patient outcomes. Key responsibilities include deep customer engagement, gathering actionable insights, and driving positive customer experiences. The role involves leveraging resources to secure access for key customers and contributing to the development of local and national brand advocates.

Roche United Kingdom

On-site Permanent