Latest Operations Analyst - Internship Jobs

Director, Clinical Science – Oncology Clinical Development

Lead scientific strategy for oncology clinical studies, contributing to protocol design, data interpretation, and regulatory documentation within a global matrix team. Focus on advancing cancer therapies with high unmet need through rigorous clinical development and cross-functional collaboration. Emphasis on scientific excellence, real-world impact, and innovation in patient-focused drug development.

GSK PLN 472,500 – PLN 787,500 pa

Hybrid Permanent

Director, Clinical Science – Oncology Clinical Development

Leads scientific components of oncology clinical studies, contributing to protocol design, data interpretation, and regulatory documentation within a defined clinical programme. Works closely with cross-functional teams to ensure scientific rigor and alignment with development goals. Focuses on generating robust clinical insights to advance cancer therapies in high unmet need areas.

GSK US$189,750 – US$316,250 pa

Hybrid Permanent

Sr. Manager, Site Budgets and Contracts

This role involves leading the creation and management of investigator site budgets and contracts for global clinical trials, using Grants Manager and FMV benchmarking tools. The Senior Manager collaborates with CROs, Legal, and Clinical Operations to ensure site budgets align with study forecasts and are executed on time. Responsibilities include strategic planning, contract negotiation oversight, risk identification, and process improvement within an outsourced trial model.

Moderna

Hybrid Permanent

Senior Project Specialist, Clinical Supplies

This role involves coordinating clinical supply operations for Moderna’s mRNA-based therapeutics, ensuring investigational products are labeled, packaged, and distributed efficiently to clinical sites. The specialist will work cross-functionally with vendors and internal teams to maintain supply chain compliance, support IRT systems, manage temperature excursions, and drive digital innovation in supply operations.

Moderna Oxford, United Kingdom

Hybrid 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

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

This role involves leading clinical development for internal medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapeutics. 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 expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £214,900 – £358,100 pa

On-site Permanent

Warehouse Shift Leader

Warehouse Shift LeaderOur client, a successful and dynamic Pharmaceutical Manufacturing company, is currently seeking a Warehouse Shift Leader.This is a permanent position working full time at the Great Yarmouth site.Hours:Week one* Monday to Thursday 6am to 2pm* Friday 6am to...

Todd Hayes Great Yarmouth, Norfolk, United Kingdom

Senior Clinical Trial Case Manager

Manages clinical trial case management activities, ensuring compliance with international and national regulations including GxP and pharmacovigilance standards. Oversees safety reporting, vendor performance, and case processing for serious adverse events, while acting as a key liaison for inspections and audits. Provides training, supports database enhancements, and ensures accurate coding and consistency in safety data analysis.

CSL

GLP/GCLP Vendor Oversight and QA Lead (EU)

This role focuses on end-to-end quality oversight of external vendors and suppliers involved in regulated R&D activities, ensuring compliance with GLP, GCP, GMP, and GVP standards. The individual will lead vendor qualification, audit management, quality agreement negotiation, and continuous performance monitoring, while collaborating with cross-functional teams including Clinical, CMC, Safety, and Legal. A key aspect is driving compliance, data integrity (ALCOA+), and continuous improvement across third-party partners through risk-based assessments, CAPA follow-up, and QMS integration.

CSL United Kingdom

On-site Permanent

Senior Alliance Manager, London

This role involves managing strategic partnerships in a cutting-edge AI-driven drug discovery environment, ensuring scientific and commercial success. The Senior Alliance Manager will oversee alliance governance, drive collaboration frameworks, and support high-impact partnerships from research to development. A key focus is fostering strong relationships between internal teams and external partners while advancing best practices in alliance management.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Senior Scientist Biomarker Lead

This role involves designing and delivering biomarker strategies and assays to support clinical development in respiratory and immunologic diseases. The scientist will lead biomarker studies using human biospecimens, interpret complex datasets, and provide evidence-based recommendations to guide trial design and patient selection. Working at the interface of lab science and clinical development, the role emphasizes assay development, cross-functional collaboration, and the application of advanced translational technologies.

AstraZeneca Cambridge, United Kingdom

Senior Scientist – Diagnostic Deployment

This role involves hands-on development, optimisation, and validation of tissue-based diagnostic assays, primarily using histology and immunohistochemistry (IHC), to support AstraZeneca's clinical trials. The scientist will integrate digital and computational pathology tools, ensure compliance with regulatory standards like CAP/CLIA and ISO, and enhance laboratory workflows through LIMS integration. The position emphasizes scientific rigour, cross-functional collaboration, and innovation in oncology diagnostics.

AstraZeneca Cambridge, United Kingdom

Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom

Engineering Manager

The Engineering Manager (Shift) leads a multiskilled team responsible for maintaining pharmaceutical equipment and utility systems in a GMP-regulated manufacturing environment. This role involves overseeing reactive and planned maintenance, managing contractors, conducting risk assessments, and ensuring compliance with GDP, ALCOA, and GMP standards. The position operates on rotating shifts and requires strong leadership, problem-solving, and technical expertise in cleanroom operations and controlled systems.

Autolus Stevenage, United Kingdom

Director, Regulatory Affairs

Lead global regulatory strategy and execution for drug development programs, ensuring compliance across jurisdictions including the US, EU, and UK. Collaborate with cross-functional teams to prepare and manage regulatory submissions such as INDs, NDAs, and orphan drug designations. Provide strategic guidance on regulatory risks and lifecycle management, while engaging with health authorities and shaping regulatory science in the context of AI-driven drug discovery.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent