Biotechnology Jobs

Clinical Development Director - Renal

The Clinical Development Director is responsible for leading and supporting the delivery of clinical deliverables for a section of a global clinical program or a large, complex trial. This role involves collaborating with various teams to ensure data quality, regulatory compliance, and scientific accuracy in clinical trials and publications.

Novartis London, United Kingdom

Hybrid Permanent

Virtual Analytics Network (VAN) PhD Graduate Program

This PhD Graduate Program at Novartis involves 15 months of rotations across three key areas of the organization, focusing on clinical trials and statistical analysis. After the rotations, you will choose a permanent role as a Principal Biostatistician, responsible for statistical work on assigned trials and implementing innovative trial designs.

Novartis London, United Kingdom

Hybrid Permanent

Director, Oncology Clinical Biomarkers

This role involves developing and implementing biomarker strategies for late-stage oncology clinical trials, collaborating with cross-functional teams to identify patient populations and optimize drug development. The Director will leverage cutting-edge technologies and methodologies to validate biomarkers and inform clinical decisions.

GSK Stevenage, United Kingdom £189,750 – £316,250 pa

On-site 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

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis London, United Kingdom

On-site Permanent

Trial Vendor Associate Director

The role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure quality and service standards are maintained throughout the study lifecycle.

Novartis London, United Kingdom

Permanent

Medical Director, Gastroenterology, Early Clinical Development

This role involves leading global clinical trial teams through phase 1 and 2 development, drafting early clinical development plans, and serving as a medical lead for early clinical studies. The Medical Director will collaborate with biomarker experts, research scientists, and key opinion leaders to identify and implement strategies for preclinical and clinical support of gastroenterology programs.

Novartis London, United Kingdom

Hybrid Permanent

Associate Director, Translational Medicine Expert, TM Clinical Pharmacology

This role involves leading and managing multiple First-in-Human and Clinical Pharmacology studies, ensuring medical and scientific excellence. You will provide expert input into study design, safety, and reporting, and collaborate with cross-functional teams to align on program objectives and optimize processes.

Novartis London, United Kingdom

On-site Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered within schedule, budget, and quality standards. The Senior Manager will collaborate with the Vendor Start-up Manager and other team members, oversee vendor interfaces, and manage risks and performance.

Novartis London, United Kingdom

Hybrid Permanent

Global Medical Affairs Director, Autoimmune Diseases

The Global Medical Affairs Director leads strategic and operational programs for autoimmune diseases, focusing on innovative evidence, launch readiness, and post-market solutions. They develop and execute medical/scientific engagement strategies, provide expert input on clinical trials, and collaborate with internal and external stakeholders to maximize the value of Novartis medicines.

Novartis London, United Kingdom

Hybrid Permanent

Vendor Start-Up Manager - eCOA & Translations

The Vendor Start-Up Manager for eCOA and Translations ensures vendors are aligned and ready to deliver high-quality services from protocol finalization to database go-live. Key responsibilities include reviewing vendor specifications, coordinating kick-off meetings, performing User Acceptance Testing, and optimizing the study start-up process.

Novartis London, United Kingdom

Hybrid Permanent

Senior Principal Biostatistician

This role involves leading the implementation of innovative trial designs and statistical models, collaborating with clinical and regulatory teams, and contributing to exploratory analyses and statistical consultations. The position requires a strong background in biostatistics and the ability to drive quantitative decision-making in clinical trials.

Novartis London, United Kingdom

Hybrid Permanent

Principal Statistical Programmer

The Principal Statistical Programmer leads statistical programming activities for large or pivotal clinical studies, ensuring high-quality and timely deliverables. They collaborate with cross-functional teams, mentor other programmers, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent

Assoc Director, Statistical Programming

The Associate Director, Statistical Programming, leads all statistical programming aspects for one or more drug development programs, ensuring cross-functional collaboration, resource allocation, and regulatory compliance. They coordinate activities, mentor programmers, and represent the team in audits and Health Authority meetings.

Novartis London, United Kingdom

Hybrid Permanent

Senior Principal Statistical Programmer

The Senior Principal Statistical Programmer leads statistical programming activities for multiple clinical studies or large projects, ensuring high-quality and timely deliverables. They collaborate with biostatistics, coordinate programming teams, and maintain compliance with industry standards.

Novartis London, United Kingdom

On-site Permanent