Latest IT Consulting Jobs

Director of Clinical Pharmacology Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic and pharmacodynamic principles to support drug development from early stages through registration and lifecycle management. Develop population PK/PD and exposure-response models, guide dose selection, and present evidence to regulatory bodies. Work within cross-functional teams while maintaining hands-on involvement in quantitative analysis and strategic decision-making.

GSK Stevenage, United Kingdom £183,150 – £305,250 pa

Director of Clinical Pharmacology Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for infectious disease assets, applying pharmacokinetic/pharmacodynamic and exposure-response modelling to inform dose selection, trial design, and regulatory strategy. Work across development phases from early planning to lifecycle management, with a strong emphasis on hands-on quantitative analysis and scientific leadership within a cross-functional environment.

GSK Canterbury, United Kingdom US$183,150 – US$305,250 pa

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and core documentation for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will lead cross-functional discussions, ensure regulatory compliance, and translate clinical data into accurate, consistent labelling content for global markets. They will also support health authority interactions and contribute to risk assessment and audit readiness.

Novartis

Hybrid Permanent

Precision Medicine Director

Leads the development and execution of precision medicine strategies within global clinical programs, focusing on biomarker and diagnostic initiatives to support patient selection and regulatory submissions in neuroscience. Acts as a scientific expert, leading cross-functional teams and ensuring compliance with medical device regulations. Facilitates collaborations with external research partners and drives operational excellence in biomarker strategy implementation.

Novartis

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing, executing, and interpreting global clinical studies to support regulatory submissions. The individual will act as a key clinical leader, collaborating with cross-functional teams and external stakeholders to shape clinical development plans, trial design, and lifecycle strategies. Expertise in obesity, endocrinology, or chronic weight management is required, along with leadership in managing large-scale clinical programs and regulatory deliverables.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountable leader for global drug development programs. The position involves end-to-end responsibility for clinical strategy, trial design, regulatory submissions, and cross-functional team leadership across a complex matrix environment. It also includes engagement with external stakeholders, patient advocacy groups, and oversight of safety and lifecycle planning, with a focus on obesity and related therapeutic areas.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Variation Planning Process Manager

The Variation Planning Process Manager will lead the design and implementation of Variation Planning processes within GSK’s ERP Evolution Programme, focusing on S/4HANA integration across Rx and Vx. The role involves defining end-to-end process frameworks, aligning with cross-functional teams including PLM, Quality, and Regulatory, and ensuring compliance with supply chain and regulatory requirements. Key responsibilities include process documentation, testing, change management, and transition planning from interim to future-state operations.

GSK €81,000 – €135,000 pa

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, ensuring operational strategy aligns with scientific goals and regulatory requirements. Oversees study delivery, vendor and resourcing strategy, risk management, and cross-functional coordination. Ensures inspection readiness and high-quality data output while leading matrixed teams and influencing senior stakeholders globally.

GSK United Kingdom

Hybrid Permanent

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development in oncology with a focus on sarcoma, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety evaluation, contribute to regulatory interactions, and mentor clinical teams within a matrixed global environment. The position requires deep expertise in oncology drug development and active engagement with external scientific leaders and regulatory authorities.

GSK United Kingdom

Hybrid Permanent

Director, Clinical Operations Asset Lead

This role leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. The individual will work closely with cross-functional teams to drive decision-making, manage vendor and resourcing strategies, and ensure compliance and inspection readiness. The position requires strategic leadership, strong stakeholder engagement, and deep expertise in global clinical development and regulatory environments.

GSK £189,750 – £316,250 pa

Director, Clinical Operations Asset Lead

Leads clinical operations strategy and execution across the full lifecycle of a drug development asset, ensuring high-quality, compliant, and efficient delivery of global clinical trials. Works cross-functionally to shape development plans, manage risk, and align operational delivery with scientific and regulatory goals. Provides strategic leadership to study teams and represents clinical operations at senior governance levels.

GSK

Senior Medical Director, Oncology Clinical Development - Sarcoma

This role involves leading clinical development for sarcoma within GSK's oncology portfolio, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and represent the programme externally at scientific forums. Based on-site in Waltham, MA, the position requires integration with cross-functional teams and mentorship of clinical staff to ensure patient-centred, scientifically rigorous drug development.

GSK £284,250 – £473,750 pa

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, timely delivery of clinical studies. Works closely with cross-functional teams to align execution with scientific and regulatory goals, while managing risks, vendors, and stakeholder engagement. Focuses on patient-centric innovation and inspection readiness within a global biopharma environment.

GSK US$189,750 – US$316,250 pa

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, setting the operational strategy and ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to align study design with strategic goals, manage vendor and resourcing strategy, and maintain inspection readiness. Serves as the primary escalation point for operational and quality issues, driving governance and risk management.

GSK

Hybrid Permanent

Director, Clinical Operations Asset Lead

Leads clinical operations for a key asset across its full lifecycle, ensuring operational strategy aligns with scientific and regulatory goals. Drives study execution, vendor and resourcing strategy, and cross-functional coordination to deliver high-quality clinical data. Focuses on innovation, risk management, and inspection readiness within a global, matrixed environment.

GSK