Latest Business Development Executive - Remote Jobs

Investigator Contracts Lead, Sr. Manager

Leads clinical trial site contract negotiations and budget management for global studies, overseeing agreements and amendments with investigator sites. Acts as a key point of contact for complex contracting strategies, collaborates with legal and finance teams, and mentors junior negotiators. Focuses on risk mitigation, timeline adherence, and process improvements in a remote, matrixed environment.

Pfizer London, SW7 2AP, United Kingdom

Remote Permanent

Investigator Contracts Lead, Sr. Manager

This role leads the negotiation and execution of clinical trial contracts with investigator sites globally, managing both contractual terms and site budgets. The Senior Manager oversees complex or high-priority studies, resolves escalations, and collaborates with Legal, Finance, and pCRO partners to ensure timely site activation. It involves shaping contracting strategies, mentoring junior staff, and driving process improvements in a remote, global environment.

Pfizer Poland

Remote Permanent

Principal Programmer / Analyst

This role involves leading programming activities for complex clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, while fostering quality assurance and innovation.

GSK

Hybrid Permanent

NIS P&D Project Management, Associate Director

The NIS P&D Project Management, Associate Director role involves developing and delivering Non-Interventional Studies (NIS) project plans, managing resources, and collaborating with various functional teams to ensure accurate and aligned project schedules. Key responsibilities include maintaining data quality in Planisware, forecasting costs, and managing risks.

GSK

Hybrid Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, and representing the function in senior interactions and health authority meetings.

AstraZeneca Canterbury, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Director, Regional Ecosystem Lead (Northern Europe & UK)

This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic partnerships, and driving business development. The Director will maintain relationships with universities, incubators, and venture capital firms, and actively participate in industry events to enhance CSL's external brand and deal flow.

CSL

Hybrid Permanent

Director, Regional Ecosystem Lead (Northern Europe & UK)

This role involves leading CSL's presence in key innovation hubs across Northern Europe and the UK, building strategic relationships with biotech, academia, and investment networks. The Director will source and evaluate opportunities, lead deal teams, and represent CSL at industry events to enhance the company's reputation and deal flow.

CSL United Kingdom

Hybrid Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna Poland

On-site Permanent

Manager, Global Regulatory Science CTA

This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.

Moderna

On-site Permanent

Senior Product Manager

This role involves shaping the product strategy and roadmap for an AI-driven platform used in pharmaceutical research. You will work closely with engineering, commercial, and customer-facing teams to ensure the product delivers real-world value, while mentoring other product managers and supporting the company's growth.

Harnham - Data and Analytics Recruitment London, United Kingdom £90,000 – £105,000 pa

Remote 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

Portfolio Innovation Director - Global Clinical Operations

The Portfolio Innovation Director will lead the integration of cutting-edge technologies, particularly AI-driven solutions, into global clinical operations at Novartis. This role focuses on identifying, evaluating, and scaling innovations to improve clinical trial design, accelerate recruitment, and enhance patient access. The position requires close collaboration with cross-functional teams and external partners to deliver measurable impact across the clinical portfolio.

Novartis London, United Kingdom

Hybrid Permanent

Principal Clinical Project Manager

This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Global Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States

On-site Permanent