Latest Project Services Jobs

Associate Medical Director, Safety Evaluation and Risk Management (SERM)

This role involves providing medical and scientific leadership in the safety evaluation and risk management of GSK’s clinical and post-marketing pharmaceutical assets. The Associate Medical Director will lead signal detection, benefit-risk assessment, and pharmacovigilance strategy, ensuring robust safety oversight across global development programs. Working within a cross-functional matrix, the individual will influence safety governance, contribute to regulatory submissions, and drive evidence-based decisions to protect patient safety.

GSK €87,000 – €145,000 pa

Hybrid Permanent

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and submission dossiers for global regulatory agencies. The Principal Medical Writer will lead complex writing projects, collaborate with cross-functional teams, and translate clinical and statistical data into clear, compliant narratives. The position emphasizes leadership in document strategy, regulatory interpretation, and the use of automation tools within a hybrid work environment.

GSK Stevenage, United Kingdom CA$118,000 – CA$168,000 pa

Hybrid 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

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

Director of Clinical Pharmacology, Cambridge, MA

Lead clinical pharmacology strategy for small molecule programs in oncology and non-oncology areas, designing and executing studies from Phase 1 through late development. Utilize AI-driven models for PK/PD prediction, dose optimization, and regulatory submissions, while managing CROs and translating preclinical data into human dosing strategies.

Isomorphic Labs Cambridge, United Kingdom

Director of Nonclinical Safety, Cambridge, MA

Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.

Isomorphic Labs Cambridge, United Kingdom

Associate Director, Global Regulatory Science, CMC

This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.

Moderna

Hybrid Permanent

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

This role involves hands-on execution of immunoassay development, qualification, and clinical sample testing to support Moderna's clinical trials. The technician will prepare reagents, conduct analyses, ensure data quality, and maintain compliance with regulatory standards in a laboratory setting. The position requires full-time on-site work with occasional overtime and is embedded in a collaborative, regulated environment focused on high-quality bioanalytical output.

Moderna

On-site Contract

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12 Month University Industrial Placement Student (UIPS): Discovery Sciences

This 12-month industrial placement offers hands-on experience in drug discovery within AstraZeneca’s Discovery Sciences team in Cambridge. You’ll work on laboratory-based projects involving assay development, automation, advanced cell models, and data analysis using tools like GraphPad Prism and AI-enabled platforms. The role emphasizes collaboration, scientific communication, and contributing to innovative research in a global, inclusive environment.

AstraZeneca Cambridge, United Kingdom £28,000 pa

Security Operations Engineer

This role involves monitoring and enhancing security across endpoints, cloud platforms, and networks, with a focus on detection engineering, incident response, and threat intelligence. The engineer will develop detection rules, respond to security incidents, and collaborate with IT and research teams to integrate security into scientific workflows. Work includes tuning SIEM and EDR tools, managing vulnerabilities, and improving security posture in a high-stakes research environment.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

A

12 Month University Industrial Placement Student: Clinical Pharmacology & Safety Sciences

This 12-month industrial placement offers hands-on experience in clinical pharmacology and safety sciences within a global biopharmaceutical R&D environment. You'll work alongside experienced scientists on drug discovery projects, contributing to safety evaluation using advanced modalities like antibody-drug conjugates and PROTACs. The role involves lab-based work such as bioanalytical assay development, biomarker analysis, cell culture, and applying AI and bioinformatics tools to support real-world drug development decisions.

AstraZeneca Cambridge, United Kingdom £28,000 pa

Quality Officer (GDP)

This role involves ensuring compliance with Good Distribution Practise (GDP), ISO 9001, and ISO 13485 standards through quality assurance activities such as managing deviations, change controls, audits, and supplier verifications. The Quality Officer will support the Quality Management System, conduct investigations, review documentation, and prepare for regulatory inspections. They will work closely with internal teams and external stakeholders to maintain product quality and process safety in a regulated environment.

Adecco United Kingdom

Hybrid Permanent

Head of Quality, Pharmaceutical

Lead the quality function in a GMP-regulated pharmaceutical manufacturing environment, overseeing QA, QC, and compliance systems. Drive quality strategy, regulatory readiness, and continuous improvement across operations. Manage audits, inspections, and a high-performing team within a growing organisation.

NMS Recruit Ltd t/a Russell Taylor Group Boothstown, Manchester, M28 1LT, United Kingdom £60,000 – £65,000 pa

On-site Permanent

Associate Director, Regulatory Diagnostics

This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.

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

Hybrid Permanent

Senior Scientist – Synthetic Chemist

A Senior Scientist in Synthetic Chemistry will lead the optimisation of synthetic routes for small molecules used in novel sensor technologies, focusing on scalability and yield improvement. The role involves hands-on laboratory work, data analysis, and contribution to blue-sky research within a fast-growing startup environment. Work is conducted under QMS/GLP standards with a strong emphasis on innovation in healthcare applications.

Carbometrics Bristol, Bristol (county), United Kingdom £34,000 – £39,000 pa