Latest IT Consulting Jobs

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Contract Manager

Manages end-to-end contract processes for Investigator Initiated Studies and Supported Collaborative Studies with academic and research institutions. Responsibilities include drafting, negotiating, and finalizing agreements, resolving contractual issues, ensuring timely execution, and supporting clinical development activities within a global biopharma environment.

GSK United Kingdom
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Medical and Scientific Advisor - Specialty Care

Provides medical and scientific leadership for specialty care therapy areas in the UK, translating global strategies into local medical plans. Engages with healthcare professionals and patient groups, supports evidence generation, and ensures medical governance. Focuses on delivering patient benefit through science and collaboration in a hybrid working environment.

GSK United Kingdom

Precision Medicine Director

The role involves leading the development and execution of precision medicine strategies within global clinical programs, focusing on biomarker and diagnostic initiatives for patient selection and regulatory support. It requires close collaboration with cross-functional teams and external partners, ensuring compliance with medical device regulations and high-quality scientific delivery. The position is embedded in the Neuroscience disease area, emphasizing strategic input into clinical trial design and regulatory submissions.

Novartis London, United Kingdom
Hybrid Permanent

Precision Medicine Director

The Precision Medicine Director leads the development and execution of biomarker and diagnostic strategies within global clinical programs, focusing on patient selection and regulatory-aligned trial design. This role acts as a scientific expert, guiding cross-functional teams in neuroscience-focused initiatives and ensuring compliance with medical device regulations. The position emphasizes strategic leadership in precision medicine, with strong collaboration across clinical development, diagnostics, and external research partners.

Novartis Ardross, Alba / Scotland, IV17 0YF, 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
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12 Month University Industrial Placement Student (UIPS): Analytical Chemistry

This 12-month industrial placement involves supporting the development of pharmaceutical drugs through analytical chemistry techniques such as HPLC, GC-MS, NMR, and XRPD. You'll work within a collaborative team to deliver analytical data that supports drug development timelines, adhering to GMP and GLP standards while gaining hands-on experience in a regulated environment.

AstraZeneca Cambridge, United Kingdom £28,000 pa
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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 a focus on obesity-related therapies. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep therapeutic expertise in endocrinology or internal medicine, extensive experience in Phase 1–3 trials, and strategic input into product development, digital innovation, and patient engagement initiatives.

Pfizer
On-site Permanent
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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

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

Leads clinical development for Internal Medicine assets within Pfizer's R&D organization, with end-to-end accountability for creating and executing global clinical development plans. Serves as the primary clinical point of contact across cross-functional teams and external partners, driving trial design, regulatory submissions, and lifecycle strategy. Focuses on obesity and related therapeutic areas, integrating innovation, patient engagement, and regulatory expertise to advance drug development.

Pfizer £214,900 – £358,100 pa
On-site Permanent
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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
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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