Latest Business Development Executive - Remote Jobs

ViiV Healthcare (GSK) Senior Director, Clinical Development

As the Senior Medical Director, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1–4 studies. You will collaborate with internal and external stakeholders to advance ViiV Healthcare's mission of eradicating HIV, focusing on long-acting medicines and novel approaches to treatment and prevention.

GSK

On-site Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site 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 and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site 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 and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Senior Director, CGR Agentic AI Innovation

Lead the development and deployment of agentic AI systems within AstraZeneca’s Centre for Genomics Research to transform scientific workflows in genomics, multi-omics, and translational research. Translate cutting-edge AI advances into practical solutions that accelerate drug discovery and clinical decision-making by collaborating with scientists, clinicians, and engineers. Drive innovation through rapid prototyping, external partnerships, and mentorship across the R&D ecosystem.

AstraZeneca Cambridge, United Kingdom

Hybrid 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

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

Analytical Chemistry - Platform Modalities Leader

This role involves leading the strategic expansion and modernization of analytical chemistry platforms for complex therapeutic modalities, including small molecules, drug conjugates, and oligonucleotides. The Platform Modalities Leader will drive the adoption of new technologies, ensure robust and scalable analytical capabilities, and provide hands-on technical leadership while influencing cross-functional teams.

GSK Stevenage, United Kingdom

On-site Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Regional Regulatory Intelligence Manager

This role involves leading the regional regulatory intelligence strategy, ensuring alignment with global regulatory direction and Health Authority expectations. Responsibilities include identifying and translating regulatory intelligence into actionable insights, influencing regulatory outcomes, and driving cross-functional collaboration to embed intelligence into submission processes and templates.

GSK United Kingdom

Hybrid Permanent