Latest IT Recruitment Jobs

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, ensuring patient safety and clinical integrity. The Medical Director provides physician-level input into study design, data interpretation, and regulatory interactions, working closely with cross-functional teams and external experts. It emphasizes integration of medical expertise across clinical development, with a focus on advancing cancer treatments through innovative science and collaboration.

GSK £222,750 – £371,250 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.

GSK

Hybrid Permanent

Medical Director, Clinical Development (Oncology), Cambridge, MA

Leads clinical development strategy for oncology programs, translating AI-driven insights into actionable trial designs and serving as medical monitor. Collaborates with cross-functional teams to advance drug candidates from discovery through proof-of-concept, with responsibility for regulatory submissions and engagement with health authorities and key opinion leaders.

Isomorphic Labs England

Hybrid Permanent

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

This role involves leading the development and maintenance of global labelling strategies and core documents for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will work cross-functionally to align labelling content, interpret clinical data, and ensure compliance with global regulatory standards. Key responsibilities include supporting health authority interactions, mentoring team members, and maintaining scientific accuracy across product lifecycles.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Postdoctoral Research Scientists - Materials & Devices for Life Sciences

This role involves advancing interdisciplinary research in materials and devices for life sciences, focusing on nanopore technologies, 3D tissue engineering, and device development for clinical diagnostics and therapeutics. The scientist will design experiments, refine emerging technologies, and contribute to high-impact publications in a collaborative, well-resourced environment. Work spans molecular sciences, nanotechnology, and bioengineering to create transformative biomedical tools.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets at Pfizer, with end-to-end accountability for designing, executing, and interpreting global clinical trials. The individual will serve as the primary clinical leader on cross-functional teams, shaping development plans, supporting regulatory submissions, and engaging with external stakeholders. A strong emphasis is placed on strategic innovation, team leadership, and therapeutic expertise in obesity and endocrinology.

Pfizer

On-site Permanent

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

Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.

Pfizer £274,500 – £457,500 pa

On-site Permanent

Global Clinical Operations AI Program Associate Director

This role leads the execution and delivery of AI initiatives within Global Clinical Operations, translating innovative concepts into scalable, compliant solutions. The Associate Director will coordinate cross-functional teams, manage the AI product roadmap, and drive adoption of AI tools across clinical trial operations. It involves strong program management, change leadership, and collaboration with technology and clinical stakeholders to transform how AI enhances productivity and compliance in drug development.

Novartis London, United Kingdom £83,930 – £155,870 pa

TA Medical Lead Immunology

This role involves providing strategic medical leadership for Novartis' Immunology portfolio in the UK, shaping local medical strategy in alignment with global priorities. The Medical Lead will drive scientific engagement, lead evidence generation including real-world studies, and translate insights into actionable plans across cross-functional teams. Key responsibilities include leading medical education initiatives, supporting product launches, and fostering relationships with key external stakeholders such as medical experts and patient organisations.

Novartis London, United Kingdom £67,900 – £126,100 pa

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

GCP Compliance Director (EMEA Hub)

This role leads Good Clinical Practice (GCP) compliance across Novartis' EMEA clinical operations, ensuring trials meet regulatory, quality, and ethical standards. The director oversees audits, inspections, and compliance events, while developing a high-performing team and driving risk mitigation. They will partner with global clinical and quality leaders to strengthen inspection readiness and operational excellence in a hybrid working environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

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

Leads clinical development for assigned internal medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. Oversees cross-functional teams to design and deliver clinical trials supporting regulatory submissions, while providing therapeutic expertise in obesity and endocrinology. Engages external stakeholders and contributes to regulatory strategy, safety reporting, and product labeling.

Pfizer £214,900 – £358,100 pa

On-site Permanent

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

This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, serving as the primary clinical accountability point on the Global Medicine Team. The leader designs and executes global clinical development plans, guides cross-functional teams through trial phases, and supports regulatory submissions and lifecycle strategies. Emphasis is placed on innovation, patient engagement, and strategic external collaboration to advance obesity and internal medicine therapeutics.

Pfizer

On-site Permanent

Senior Principal Statistical Programmer

Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.

Novartis London, United Kingdom

On-site Permanent