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 deliverables within a global pharmaceutical environment. Collaborate across functions to ensure scientific rigor and alignment with clinical development goals, while engaging with external experts and supporting regulatory submissions. The role emphasizes innovation, data-driven decision-making, and continuous improvement in clinical development processes.

GSK £189,750 – £316,250 pa

Hybrid Permanent

Director, Clinical Science – Oncology Clinical Development

Lead scientific contributions to oncology clinical studies, focusing on protocol design, data interpretation, and regulatory documentation within a global matrix team. Provide expert input to clinical development plans and collaborate with cross-functional teams to advance cancer therapies. Engage with external experts and support regulatory submissions to drive patient impact.

GSK PLN 472,500 – PLN 787,500 pa

Hybrid Permanent

VP, Clinical Operations and Data Management

Leads the end-to-end delivery of global clinical trials from start-up to close-out, ensuring compliance, data integrity, and on-time execution. Oversees clinical operations and data management functions, including vendor and site management, database design, and regulatory coordination. Focuses on strategic planning, cross-functional collaboration, and team development within a regulatory-compliant environment.

Orchard Therapeutics London, United Kingdom

Hybrid

Specialist, R&D Contracts & Business Operations

This role supports R&D contract management and business operations within a global biopharmaceutical organization. The specialist will handle end-to-end contract processes including drafting agreements, managing purchase orders, ensuring compliance, and maintaining accurate records. Collaboration with cross-functional teams is essential to track obligations, ensure timely approvals, and promote operational efficiency in a hybrid working environment.

CSL

Hybrid Permanent

Director, Resilience Lifecycle & Supply Chain Operations

Leads end-to-end product lifecycle management, launch planning, and supply chain operations across the UK, Canada, and Australia, ensuring alignment between global strategy and local execution. Establishes governance, performance standards, and escalation frameworks while driving operational resilience, compliance, and cross-market collaboration. Focuses on S&OP, business continuity, crisis preparedness, and digital transformation through analytics and automation.

Moderna

Sr. Manager, Site Budgets and Contracts

This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.

Moderna Oxford, United Kingdom

PV Systems and Processes Lead x2

This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.

CSL United Kingdom

On-site Permanent

Senior Finance Business Partner - Alexion

This role involves leading financial strategy and business partnering for a designated disease area across the UK and Ireland, with full P&L responsibility. The Senior Finance Business Partner will drive forecasting, performance management, and financial governance, using AI and advanced analytics to inform decisions on pricing, reimbursement, and market access. Close collaboration with cross-functional teams ensures strategic alignment and effective delivery of patient-focused therapies.

AstraZeneca London, United Kingdom

On-site Permanent

Product Manager

Product ManagerCambridgeUp to £70,000 + benefitsRole Overview: Product Manager:The company is looking for a technically competent Product Manager to lead global commercial and strategic activities for their range of scientific products used in the food & beverage markets. The role...

Marcus Webb Associates Limited Cambridge, Cambridgeshire, United Kingdom £60,000 – £70,000 pa

Head of Quality - Pharmaceuticals

Leads quality assurance and control functions within a pharmaceutical manufacturing and import environment, ensuring compliance with EU GMP standards. Responsible for maintaining inspection-readiness, managing regulatory audits, and serving as the primary liaison with the MHRA. Develops and drives the site's Quality Management System as a member of the Site Leadership Team.

Smart4Sciences Manchester, United Kingdom £60,000 – £65,000 pa

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 therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

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

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

Senior Director, Facilities Engineering

Leads the end-to-end design, build, and commissioning of a clinical-stage GMP gene therapy manufacturing suite, ensuring compliance with EU GMP Annex 1 and other regulatory standards. Provides strategic oversight of facilities engineering, maintenance, and contamination control, while managing cross-functional teams and vendor relationships. Ensures operational readiness, regulatory compliance, and continuous improvement across both manufacturing and corporate facilities.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

Scientist 2 - Analytical

Perform analytical testing on medical devices, skincare products, and raw materials using techniques like HPLC, FTIR, and ICP-MS. Support method development, validation, and compliance with ISO 13485 and GMP standards. Contribute to R&D projects, maintain laboratory equipment, and ensure accurate data reporting and documentation in a regulated environment.

Carbon 60 Deeside, Clwyd, United Kingdom £132 – £142 pd

On-site Contract

Head of Engineering

This role involves leading and scaling the Engineering team, establishing strong engineering processes, and providing architectural oversight for a sophisticated AI-driven platform used by leading pharmaceutical companies. The position offers significant impact and ownership in a high-growth Series A business.

Harnham - Data and Analytics Recruitment London, United Kingdom £120,000 – £130,000 pa

Remote Permanent