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Pharmacometrics Lead, AI and Machine Learning We are looking for an innovative and agile Pharmacometrics Lead (AI and Machine Learning) to join a Quantitative Clinical Pharmacology group. About the role You will lead the Pharmacometrics AI and ML strategy to support the development of a growing portfolio. This includes dose selection, trial design, extrapolation where appropriate, PIP development, and the ongoing evaluation of emerging clinical data across programs. What you’ll be responsible for • Developing, implementing, and leading AI and ML strategy within Pharmacometrics and Quantitative Clinical Pharmacology, • Evaluating and adopting emerging technologies across pharmacometrics and quantitative clinical pharmacology, • Performing hands-on AI and ML, population PK/PD, exposure response modeling, and clinical trial simulations on project teams, • Delivering submission‑ready, fit‑for‑purpose pharmacometrics analysis plans and reports, • Initiating and overseeing outsourced pharmacometrics and AI and ML work, with responsibility for internalizing activities where appropriate, • Supporting and mentoring the development of the pharmacometrics team from both a scientific and technical perspective, • Applying state‑of‑the‑art methodologies to optimize drug discovery and development, • Working across global regulatory pathways, including engagement with health authorities and external working parties, particularly in Paediatrics, Neurology, and Immunology, • Partnering closely with QCP Leads to ensure full integration of pharmacometrics into development programs, • Promoting MID3 principles internally and externally What we’re looking for • PhD or MD in pharmaceutical sciences, statistics, engineering, or a related discipline, • 8+ years of industry experience in pharmacometrics, with at least 2 years applying AI and ML in drug development, • Strong hands‑on expertise in population PK/PD, disease progression modeling, and clinical trial simulation, • Deep understanding of Bayesian methodologies and model‑based meta‑analysis, • Practical experience with R, Python, Matlab, NONMEM, or related pharmacometrics tools, • An agile mindset with the ability to prioritize and adapt across multiple projects, • Excellent communication, collaboration, and presentation skills Interested in shaping the future of Pharmacometrics through AI and ML? This role offers the opportunity to lead scientifically, influence strategy, and work across global development programs.

This is an excellent opportunity to join a successful pharmaceutical company within the Global HTA and Payers organisation. Reporting to the Global Access Strategy Lead, you’ll collaborate closely with cross-functional teams to deliver key global materials, with a particular focus on the Market Access Strategy Summary. This role offers strong exposure to asset-level strategy, global–local collaboration and is well-positioned as a stepping stone for future leadership within Market Access. Key Responsibilities • Lead development of core payer deliverables (GVDs, DARs, value narratives), • Support and enable the Market Access Strategy Summary (MASS), • Align cross-functional evidence generation (HEOR, RWE), identifying evidence gaps and access risks, • Partner with global, regional and local teams to drive access strategy, • Contribute to scientific communication and external engagement Candidate profile: • Relevant degree in Health Economics or equivalent, • Strong background (7+ years) in market access within the biopharmaceutical industry or consulting space (e.g. HTA, HEOR, outcomes research, payer evidence, or access strategy), • Experience supporting global or asset-level payer evidence or access projects, • Affiliate or country-level experience, particularly supporting HTA submissions or payer interactions, • Understanding of payer and HTA decision-making processes in at least one major market This role is offered on an initial 12 month contract with realistic potential for extension. Keywords: Pharmaceutical, clinical trial, market access strategy, payer evidence, GVDs, global value dossier, DARs, detailed assessment reports, value narratives, evidence synthesis, London, Oxford, Reading, Slough

A leading global clinical research organization is seeking a CQA Auditor to ensure compliance and accuracy of clinical trial data.You will conduct external audits, develop comprehensive reports, and identify risks impacting trial integrity.The ideal candidate has substantial quality assurance experi

A leading biotechnology company is looking for a Principal Statistical Programmer in Maidenhead, UK.The role involves expert-level programming support in SAS, along with the potential for R programming for clinical trial data analysis.Responsibilities include writing and validating datasets, adherin

The Principal Statistical Programmer will provide expert-level hands‑on principal programming support and technical leadership to develop, maintain, validate and run SAS computer programs that access, visualize, analyze, and report clinical trial data, in accordance with statistical analysis plans

Key Words: Associate Clinical Project Manager / Clinical Research / Clinical Studies / Trial Coordination / Clinical Project Support / Life Sciences / Clinical Operations / Study Documentation / Clinical Systems / Regulatory Requirements / Pharma / Pharmaceutical / Biopharma / CRO / clinical / proje

Planet Pharma is seeking an Associate Clinical Project Manager based in Slough for a hybrid role.The position involves supporting the planning, execution, and close-out of clinical trials while managing cross-functional teams.Candidates should have a Bachelor’s degree in life sciences or healthcar

A leading global biopharmaceutical company seeks a Country Clinical Operations Manager to oversee clinical trial management in Maidenhead.

For many, taking part in clinical research offers hope, purpose, and a chance to shape the future of dementia care. But finding the right trial, understanding what it involves, and knowing how to take part can be confusing.

Our client is a global pharmaceutical organisation conducting novel drug discovery & development projects across a broad range of therapeutic areas including Neuroscience, Inflammation, Immunology and Oncology etc. In this role you will be supporting the delivery of clinical studies from protocol development through to final reporting and archiving. It’s a great opportunity for someone early in their clinical research career who enjoys organisation, collaboration, and continuous improvement. Working closely with the Clinical Project Manager, you will help ensure studies run smoothly by coordinating plans, documentation, systems, and partners. You’ll play a central role in keeping teams aligned, maintaining high-quality records, and ensuring timelines and regulatory requirements are met. Key responsibilities • Maintain an accurate and audit-ready Trial Master File (TMF) through ongoing review and follow-up, • Support the preparation, review, and finalisation of key study documents (e.g., protocols, amendments, consent forms, plans, submissions, and reports), • Coordinate meetings, communications, and decision tracking across cross-functional teams and external partners, • Assist with oversight of vendors and investigational sites, including training coordination and issue resolution, • Set up and maintain study data in clinical systems, perform quality checks, and respond to system queries Key requirements • Bachelor’s degree (or equivalent) in a relevant scientific, healthcare, or business discipline, • 1–2 years’ experience in clinical research (e.g., trial coordination, monitoring support, or project support), • Exposure to clinical trials across phases I–IV is advantageous, • Strong attention to detail with the ability to manage multiple priorities, • Confident using office tools and clinical systems, with a focus on data quality, • Clear, professional communication skills and ability to work across global teams, • Proactive, organised, and keen to learn, with a practical approach to problem-solvingAssociate Clinical Project Manager

A leading clinical research organization in London is seeking a Clinical Trial Manager to oversee clinical projects, primarily focusing on Nephrology. Candidates with a passion for clinical trials and at least 5 years of experience in managing such projects are encouraged to apply.

The role is responsible for providing advanced expertise in feasibility and site intelligence processes to inform clinical trial planning and execution across the Jazz clinical trial portfolio. Subject matter expert in oncology global clinical trial feasibility and site intelligence to support opera

This position offers opportunities to support a variety of clinical trials while working collaboratively in a dynamic team environment.

Candidates should possess a Bachelor's degree in a related field and have 3-4 years of clinical trial experience, particularly in Early Phase studies.

The Senior Clinical Trial Manager, Clinical Operations, serves as the operational lead for assigned early-phase oncology studies, providing end-to-end trial leadership from start‑up through close‑out. Provide end‑to‑end operational leadership for complex, multi‑regional clinical trials fro

Be part of a high-growth organisation where your work directly supports clinical trials and patient outcomes. Sourcing Director OR Sourcing Manager - Clinical Trial Supplies. Director of Clinical Supplies / Supply Chain Director / Head of Purchasing / Comparator Sourcing / Sourcing Manager / Senior

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

The Clinical Trial Supply Chain Manager is responsible for overseeing the supply chain and logistics of clinical trial materials to ensure timely and efficient delivery to sites across the globe. Strong knowledge of GCP (Good Clinical Practice), GMP (Good Manufacturing Practice), and regulatory requ

This full-time role involves being an internal and external SME for clinical trial design and statistical consultancy for clients. You will work with innovative statisticians, engage with clients, and oversee the application of statistical methods, contributing to the development of cutting-edge tri

Harrington Recruitment is seeking a Senior Sales Representative/BDM in the clinical trial services sector. The ideal candidate will have over 6 years of experience in life sciences, with a focus on clinical development.

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Want to join a fast-paced, exciting department working with some of the biggest names in healthcare? At Lang

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

Job Description:**Job Title:Director, Clinical Trial Management SystemsDivision / Function:Clinical Trial Excellence, Clinical Development OperationsManager’s Job Title:Head of Clinical Trial ExcellenceLocation:London, UK - Paris, France - Cambridge, USWHAT - **Summary & Purpos

A leading clinical research organization in London is seeking a Director of Clinical Trial Management. The ideal candidate has minimum 5 years of experience in clinical trial management, preferably in a CRO, with strong leadership skills. You will manage day-to-day operations, ensuring compliance wi

In this role, you will create impactful campaigns for clinical trials, manage vital client relationships, and ensure the success of global health initiatives.

A clinical trial consultancy in the United Kingdom is looking for a skilled statistical lead to oversee clinical trial programs/projects. Master’s degree in statistical science or a related field, along with demonstrated experience in clinical trial projects. You will provide statistical methodolo

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Cardiovascular/Endocrine/Metabolic are welcome to continue to work in thei

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Work with the clinical trial management staff to support

The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study

A leading healthcare communications agency is seeking an experienced Account Manager to oversee client services in clinical trial campaigns.

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Communicate and collaborate on globa

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Langland, a Publicis Health company, is the only health communications agency that thinks further across Cli

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Clinical Trial Managers with expertise in Nephrology are welcome to continue to work in their area of expertise or t

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. All materials we create are translated and rolled‑out in each country supporting the clinical trial. Langl

Assist in the clinical trial insurance process; track approvals, revisions and renewals of certificates. Minimum of 3‑4 years of progressive clinical trial experience. Lead the preparation of country specific agreements, confidentiality agreements, clinical trial applications and other applicable

The role involves creating impactful materials for clinical trials aimed at improving lives.

A leading health communications agency in Greater London seeks an experienced Account Manager to oversee campaigns for clinical trial recruitment.

To date, we've supported over 800 clinical trials in more than 290 conditions over 75 countries, helping to convert over 500,000 patients to a clinical trial at a time when they need it most. Want to join a fast‑paced, exciting department working with some of the biggest names in healthcare? At La

A leading life sciences company in London is seeking a Clinical Trial Manager to oversee the development and execution of Phase III clinical studies across Europe. The role requires strong project management and organizational skills, as well as familiarity with clinical trial management software.

Support the Principal Pharmacist for Clinical Trials in the provision and development of the clinical trials service, ensuring that all regulatory requirements for Investigational Medicinal Products (IMPs) are met. The successful applicant should have experience working in clinical trials, including

Provide cross‑cover for other research nurses, trial practitioners, data managers and assistants working in the clinical trials unit as directed by the Clinical Trials Manager. The post holder will take responsibility for the co‑ordination and management of a clinical research portfolio comprisi

A prominent health communications agency in Greater London seeks an experienced Account Manager to oversee day-to-day client management and ensure effective delivery of projects.The ideal candidate will have a strong background in healthcare accounts, exceptional communication skills, and the abilit

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Clinical Trial Management team. Communicate and collaborate on global study activities; working closely with the project

Clinical Trial Associate ManagerLocation: LondonAbout the Role**The Clinical Trial Associate Manager plays a key leadership role in ensuring the successful execution of clinical trials by overseeing a team of Clinical Trial Associates (CTAs). Clinical Trial Associate Manager page is loaded##

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Clinical Trial Management team. Compile and maintain project-specific status reports within the clinical trial managemen

Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role. Exposure to multiple complex therapeutic areas and global clinical trial operations. Strong understanding of clinical trial documentation, TMF management and regulatory processes.