Latest Business Development Executive - Remote Jobs

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the end-to-end development of oncology drugs.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of phase 1-3 clinical trials for hematological malignancies. This role involves collaborating with a multi-disciplinary team to ensure patient safety, scientific integrity, and regulatory compliance, while contributing to the strategic development of GSK's oncology portfolio.

GSK

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 and executing clinical trials, creating development plans, and collaborating with cross-functional teams to ensure regulatory approvals and 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. This role involves designing, executing, and interpreting clinical studies, 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

Medical Affairs Lead - Lung

This role involves leading the medical input for AstraZeneca's Lung Oncology portfolio, developing and delivering medical plans, and maintaining scientific relationships with key customers. The Medical Affairs Lead will also ensure regulatory compliance and support market access activities, working closely with the Therapy Area Medical Team to drive innovation and excellence.

AstraZeneca London, United Kingdom

Hybrid 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, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. The Director will guide cross-functional teams in designing and validating digital biomarkers, collaborating with external partners, and enhancing the efficiency and patient-centricity of GSK's clinical trials.

GSK

On-site Permanent

Director, Digital Medicine: Respiratory, Immunology & Inflammation Research Unit

This role involves leading the development and implementation of digital medicine strategies to support clinical programs and studies in respiratory, immunology, and inflammation. The Director will guide cross-functional teams in designing digital biomarkers, endpoints, and measures, and collaborate with external partners to enhance clinical trial efficiency and patient-centric outcomes.

GSK Exeter, EX4 4HD, United Kingdom

On-site Permanent

SERM Scientific Director

The SERM Scientific Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. This role involves driving pharmacovigilance activities, evaluating safety data, and collaborating with cross-functional teams to ensure robust benefit-risk profiles and patient safety. The position requires significant experience in pharmacovigilance and a strong understanding of global regulations.

GSK

On-site Permanent

Programming Leader

The Programming Leader role involves overseeing project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion the adoption of agile principles and new technologies to improve efficiency and data analysis.

GSK Stevenage, United Kingdom

Hybrid Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways, ensuring biomarker datasets are reusable and accessible. Key responsibilities include resolving systemic barriers, aligning data delivery with decision timelines, and developing repeatable processes for data re-use across multiple functions.

GSK Stevenage, United Kingdom

Hybrid Permanent

Programming Leader

The Programming Leader will oversee project-level and study-level programming strategy and delivery for multiple complex studies in GSK's global pipeline. You will collaborate with cross-functional teams, ensure high-quality outputs, and champion agile methodologies and new technologies to enhance programming efficiency and data analysis.

GSK

Hybrid Permanent

Manager, Translational Biomarker Data Pathways & Re-use

This role involves leading the setup, stabilization, and scaling of end-to-end translational data pathways at GSK. Key responsibilities include ensuring biomarker datasets are reusable, accessible, and aligned with translational decision-making, while also identifying and resolving systemic barriers and developing repeatable processes.

GSK

Hybrid Permanent

SERM Medical Director

The SERM Medical Director at GSK leads the safety evaluation and risk management of oncology assets in clinical development. Key responsibilities include interpreting safety data, managing safety signals, and providing expert medical input to support benefit-risk decisions. This role involves leading cross-functional teams, collaborating with regulatory authorities, and shaping the safety strategy for innovative oncology medicines.

GSK

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.

Pfizer Sandwich, United Kingdom

On-site Permanent