Latest Operations Analyst - Internship Jobs

Clinical Operations Specialist (NCVR & Contracts)

This role involves leading the coordination and lifecycle management of clinical trial contracts and legal documents in compliance with ICH GCP, UK regulations, and GSK standards. The specialist will negotiate investigator and supplier contracts, manage budget development, ensure TMF completeness, and act as a point of contact for legal and contracting issues. The position supports clinical operations through digital tools, including AI-enabled solutions and CLM platforms, while providing training and administrative support to local and global teams.

GSK United Kingdom

Inspection Assembly & Packaging Operations Manager

Lead inspection, assembly, and packaging operations in a regulated pharmaceutical environment, ensuring safety, quality, and on-time delivery. Drive continuous improvement, coach frontline teams, and support new product introductions in collaboration with engineering and quality teams. Operate within a GMP-compliant manufacturing site with a focus on compliance, efficiency, and people development.

GSK Barnard Castle, United Kingdom

On-site Permanent

Senior Manager, Packaging Engineering

Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

Design and optimize automated workflows for clinical biomarker testing and sample management using advanced liquid handling platforms and integrated data systems. Lead automation integration, troubleshooting, and digital connectivity across laboratory operations, ensuring compliance and scalability. Support AI-enabled workflows and mentorship within a regulated, innovation-driven environment.

Moderna Oxford, United Kingdom

Hybrid 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, with accountability for designing and executing global clinical development plans. The individual will guide cross-functional teams through trial design, regulatory submissions, and lifecycle management, while serving as a therapeutic expert and strategic partner across internal and external stakeholders. Emphasis is placed on innovation, patient engagement, and compliance with global regulatory standards.

Pfizer £214,900 – £358,100 pa

On-site Permanent

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

This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, serving as the primary clinical accountability point for global regulatory submissions. The individual will direct cross-functional teams in designing and executing Phase 1-3 trials, develop clinical development plans, and contribute to regulatory filings, safety reports, and product labeling. The position emphasizes leadership in obesity-related therapeutics, digital innovation in clinical development, and engagement with external scientific and regulatory stakeholders.

Pfizer

On-site Permanent

Senior Director, Alliance and Integration Management

Leads integration and alliance management for high-priority pharmaceutical acquisitions, divestitures, and strategic partnerships. Drives cross-functional alignment across legal, finance, clinical, and commercial functions to ensure successful post-deal execution and value delivery. Develops industry-leading processes and represents the company as a thought leader in alliance management.

AstraZeneca Cambridge, United Kingdom

Senior Quality Associate – Accredited Diagnostic Development Laboratory

This role involves leading quality management within AstraZeneca’s accredited internal diagnostic laboratory, ensuring compliance with CAP/CLIA, IVDR, and ISO standards during the development and validation of precision diagnostic assays. The Senior Quality Associate will drive change control, investigation of non-conformances, CAPA management, and audit readiness, while collaborating closely with lab scientists and regulatory teams. The position plays a key role in enabling biomarker-driven clinical trials through robust, patient-ready diagnostic solutions.

AstraZeneca Cambridge, United Kingdom

Senior Software Engineer (Inference Platform), London

This role involves leading the reliability and scalability of AI/ML infrastructure for biotech applications, focusing on GPU/TPU systems, workload orchestration, and inference services. The engineer will overhaul monitoring, improve CI/CD stability, and ensure robust platform performance to support cutting-edge drug discovery research. Close collaboration with research and applied ML teams is central to the role.

Isomorphic Labs London, United Kingdom

On-site Permanent

Director, Clinical Science

Lead clinical strategy and execution for early-phase trials, authoring key clinical documents and overseeing medical monitoring. Serve as primary liaison with investigative sites and internal teams, ensuring data integrity across multiple oncology and hematology studies. Operate in a fast-paced, AI-driven drug discovery environment with cross-functional collaboration.

Recursion United Kingdom US$212,900 – US$287,980 pa

Remote Permanent

Software Engineer (TechOps), London

This role involves building and managing cloud infrastructure and DevOps tooling to support AI-driven drug discovery. You'll work across research, development, and production environments using GCP, Kubernetes, and Infrastructure as Code, collaborating closely with scientists, ML researchers, and engineers. The focus is on creating scalable, secure, and automated systems that accelerate scientific innovation in a fast-moving, interdisciplinary environment.

Isomorphic Labs United Kingdom

Hybrid Permanent

Bio-ML Scientist (Metabolic Modelling) - Generative Biology Institute

Develop and deploy machine learning systems to advance synthetic biology, genome design, and metabolic modelling in close collaboration with wet lab scientists and computational teams. Focus on building scalable, biology-centric AI solutions using diverse data modalities and integrating with genome-scale metabolic models. Work within a multidisciplinary research environment to co-create projects and drive innovation from concept to publication.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

Media and Glass Technician - Generative Biology Institute

This role involves preparing laboratory media, buffers, and agar plates while maintaining sterile glassware and consumables to support high-quality research at the Generative Biology Institute. The technician ensures consistent, contamination-free supplies using aseptic techniques and standard operating procedures, enabling scientists to focus on engineering biology breakthroughs. The position emphasizes precision, routine quality control, equipment operation, and collaboration within a dedicated support team in a state-of-the-art research environment.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Validation/ Quality Assurance Specialist, Pharmaceutical

The Validation/Quality Assurance Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.

NMS Recruit Ltd t/a Russell Taylor Group Swadlincote, Derbyshire, DE11 0AG, United Kingdom £30,000 – £34,000 pa

On-site Permanent

Head of Quality / Senior Quality Manager - Pharmaceutical

This role involves leading the entire Quality function (QA and QC) within a pharmaceutical manufacturing site, overseeing a team of 15 and ensuring strict adherence to GMP and regulatory standards. The individual will drive the site's Quality strategy, manage audits and inspections (including MHRA and customer audits), and lead continuous improvement initiatives across quality systems, validation, and compliance. With a strong emphasis on leadership and team development, the role sits at the heart of the site’s leadership team and requires strategic oversight alongside hands-on operational involvement.

Radar Recruitment Manchester, United Kingdom £60,000 pa