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Overview Our client is a fast-growing, global brand in the health, fitness, and sports nutrition sector, expanding rapidly across the UK. Reporting to the UK Head of Sales, the Key Account Manager will lead growth within the Gym & Independent channel, owning commercial performance across independent gyms, specialist sports nutrition retailers, and regional distribution partners. This is a highly entrepreneurial, field-focused role with full ownership of sales results, distribution expansion, and promotional execution. Working closely with cross-functional partners, including Marketing, Supply Chain, and Finance. You will play a key role in scaling the brand’s presence within one of the UK’s fastest-growing channels. Responsibilities • Deliver and exceed revenue, profit, and distribution targets in line with UK growth plans., • Manage, strengthen, and grow relationships with distribution partners, acting as the primary commercial contact., • Expand distribution across specialist retailers and independent gym networks, driving sell-through via distributor partners., • Build and execute a channel promotional calendar aligned with national strategy., • Develop a structured contact plan, capturing customer interactions, competitor activity, and new business progress., • Be field-based at least three days per week, visiting key accounts and prospective customers across the UK., • Collaborate with Marketing to implement in-store activation, sampling programmes, and brand-building initiatives., • Host sampling events in gyms and specialist stores to boost trial and awareness., • Manage internal order processing and ensure smooth operational execution., • Provide accurate forecasting inputs and support monthly S&OP processes with a focus on demand-planning accuracy., • Track and report on sales performance, distribution growth, promotional ROI, and market opportunities., • Represent our client at industry events, expos, competitions, and trade shows domestically and internationally. Qualifications • Experience in account management, field sales, or distribution within FMCG, sports nutrition, or related categories., • Strong commercial mindset, motivated by achieving targets and owning channel performance end-to-end., • Proven ability to build long-term customer relationships and grow accounts strategically., • Highly organised with strong planning, reporting, and communication skills., • Comfortable working independently while collaborating effectively with cross-functional teams., • Proficient in Microsoft Excel, PowerPoint, and Word., • Solution-oriented approach with the ability to resolve customer challenges professionally., • Industry knowledge in sports nutrition or fitness is beneficial but not essential., • Passion for health, fitness, or sports is a must.

QA Regulatory Manager Site‑based with flexibility for some remote working in the long‑term Locations: Flexible - can be based out of Sheffield, Preston, Stoke‑on‑Trent or Manchester Are you an experienced QA and Regulatory professional ready to take on a pivotal leadership role within an exciting growing business? Our client is looking for a QA Regulatory Manager to oversee regulatory affairs for the UK business and assist with QA projects. Reporting directly to the Head of Quality, this is a key strategic position interfacing with Quality Assurance, Regulatory Affairs, Operations and external regulators. You’ll play a critical role in shaping quality systems, ensuring inspection readiness, and supporting the development and supply of Investigational Medicinal Products (IMPs). What you’ll do: • Provide QA and regulatory leadership across all UK 6 facilities, ensuring consistent application of GMP, GDP and MHRA requirements., • Act as the regulatory lead for IMP development activities, including review and approval of IMPDs, clinical trial quality documentation and supply processes., • Lead interactions with MHRA and other regulatory bodies, supporting inspections, audits, responses and ongoing compliance commitments., • Ensure site licences, variations and regulatory submissions remain current and aligned with operational activities., • Harmonise and strengthen quality systems across multiple sites, covering deviations, CAPAs, change control, documentation and risk management., • Provide QA project support for product development, technology transfer and validation activities within sterile production environments., • Review and approve quality documentation, including SOPs, validation protocols, batch records and development reports., • Serve as subject matter expert for aseptic GMP, IMP manufacture and regulatory expectations. What you’ll bring: • Proven Regulatory Affairs experience within sterile manufacturing or aseptic environments (5 years+), • Proven QA management experience, • Hands‑on experience supporting IMP development, clinical trial supply and IMPD preparation/review., • Strong working knowledge of UK/EU GMP, MHRA regulatory requirements and GxP compliance., • Background in regulatory inspections, audits and authority interactions., • Ability to work effectively with manufacturing, QC, development and clinical teams., • Degree in a scientific discipline (or equivalent experience); further QA/regulatory qualifications are an advantage., • Excellent communication skills, able to influence and collaborate at all levels. Why Apply? This is a rare opportunity to take on a high‑impact role within a specialised and mission‑driven aseptic pharmaceutical operation. You’ll shape the regulatory framework supporting both commercial products and innovative clinical development programmes—while working with a collaborative, highly skilled team committed to improving patient outcomes. Key Words: Regulatory Affairs, RA, QA, quality assurance, manager, senior, supervision, supervisor, leader, lead, IMP, clinical, commercial, GMP, sterile, aseptic, injectables, injection, terminal sterilization, radiopharmaceutical, radiopharma, nuclear medicine.

Regulatory Quality Assurance Manager – UK Location: Manchester Permanent | On-site (5 days/week) We’re supporting a growing pharmaceutical manufacturing organisation operating across several UK sites. With expanding development programmes, evolving regulatory expectations and increased operational complexity, this is an exciting opportunity to step into a pivotal role that blends Regulatory Affairs and Quality Assurance. This role can be based in Manchester or Preston. As Regulatory QA Manager, you’ll provide regulatory leadership across multiple licensed facilities, ensuring inspection readiness, GMP/GDP compliance and robust quality systems. This is a hands‑on, influential role where you will act as the main liaison with regulatory authorities, support both commercial and IMP activities, and drive harmonisation of standards across the network. This position is ideal for a strong Regulatory professional with QA exposure who is ready to shape regulatory frameworks, strengthen quality culture and support cutting‑edge sterile product operations. Key Responsibilities: • Provide regulatory and QA oversight across multiple licensed sterile manufacturing sites, ensuring consistent GMP, GDP and MHRA compliance., • Act as the primary contact for regulatory authorities, supporting inspections, audits, submissions and ongoing compliance commitments., • Lead regulatory activities for commercial and IMP products, including review of IMPDs, pre‑submission work, post‑approval activities and clinical trial supply documentation., • Support and advise site teams on quality and regulatory improvements, inspection readiness and continual improvement initiatives., • Provide QA input into product development, validation, technology transfer and sterile processes., • Contribute to implementation of a new electronic Document/Quality Management System. Requirements: • Degree or higher in a scientific, quality or regulatory discipline (or equivalent experience)., • Extensive Regulatory Affairs experience, including IMP and clinical trial supply exposure., • Strong knowledge of UK/EU GMP, MHRA expectations and GxP compliance., • Experience in sterile manufacturing or aseptic processing., • Some Quality Assurance experience, capable of supporting QA initiatives and projects., • Experience working across multi‑site operations and regulatory inspections. We're moving quickly on this role - if you're interested, apply early as the advert may close ahead of schedule.

Business Development Manager\n\nRevolutionary SaaS | Electronic Health Records | Clinical Trials & Drug Development\n\nSalary: £50,000–£60,000 (negotiable) + uncapped commission + excellent benefits\nLocation: Home-based with access to Manchester offices (1–2 days per month)\n\nThe Opportunity\n\nThis is not just another sales role.\n\nYou’ll be joining a fast-growing UK business at the forefront of transforming how life-saving drugs are developed. With a proven track record of securing multi-million-pound transatlantic deals with leading global pharmaceutical companies, the business is scaling rapidly—and you could be a key part of that journey.\n\nIf you’re looking to sell a genuinely innovative solution, work with an exceptional leadership team, and accelerate your career in a high-growth environment, this is your chance.\n\nAbout the Company & Solution\n\nThis organisation is redefining how Electronic Health Record (EHR) data is used in clinical research.\n\nTheir cutting-edge SaaS platform analyses and interprets real-world healthcare data, turning it into powerful insights that drive smarter, faster drug development.\n\nClients—including major global pharmaceutical companies—use this platform to:\n\n * Access real-time, searchable patient data\n\n * Optimise clinical trial design and execution\n\n * Reduce development timelines and costs\n\n * Bring life-saving treatments to market faster\n\nThe impact? Tangible improvements in global health outcomes, powered by data.\n\nThe Role\n\nAs a Business Development Manager, you will play a pivotal role in driving new business growth across the pharmaceutical and CRO landscape.\n\nThis is a strategic, consultative sales position where you’ll engage senior stakeholders and build demand for a complex, high-value solution.\n\nYou’ll thrive here if you enjoy creating opportunities from scratch, navigating long sales cycles, and influencing decision-makers in a highly specialised market.\n\nKey Responsibilities\n\n * Build, manage, and convert a high-quality pipeline of new business opportunities\n\n * Identify and engage key stakeholders across pharmaceutical companies and CROs\n\n * Develop relationships with teams in clinical development, medical affairs, and real-world evidence\n\n * Lead consultative sales processes from initial engagement through to close\n\n * Articulate the value of a complex, data-driven SaaS solution\n\n * Maintain accurate pipeline visibility and forecasting via CRM\n\nAbout You\n\nWe’re looking for a driven, commercially minded sales professional who is ready to step up and make an impact.\n\nYou will have:\n\n * 1–3 years’ experience in a relevant sales or business development role\n\n * Exposure to the life sciences, pharmaceutical, or CRO market\n\n * A track record of generating new business and hitting targets\n\n * Experience selling solutions (ideally SaaS or data-driven offerings)\n\n * The ability to engage multiple stakeholders and manage complex sales cycles\n\n * A proactive, self-starting mindset with the hunger to succeed\n\nMost importantly, you’re ambitious, resilient, and excited by the opportunity to sell something that genuinely makes a difference.\n\nWhy Join?\n\n * Sell a truly innovative, market-leading solution\n\n * Be part of a company closing multi-million-pound global deals\n\n * Work directly with an experienced and supportive leadership team\n\n * Enjoy significant earning potential with uncapped commission\n\n * Accelerate your career in a high-growth, high-impact sector\n\n * Contribute to advancements in life-saving drug development

A leading clinical research organization in Greater London is seeking experienced Clinical Trial Managers to oversee projects and ensure compliance with all regulations. Candidates should have at least 5 years of experience in clinical trial management, preferably within a CRO.

A healthcare organization in Greater London is seeking a Trial Manager for the RM-CTU Breast team. The successful candidate will coordinate clinical trials, manage documentation, and support junior staff. Responsibilities include ensuring compliance with regulatory requirements and engaging with sta

The aCTM will work with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Communicate and collaborate on global study activities; working closely with the Project Coordinator and Clinical Trial Manager. Candidates should expect to have an intens

Impact and Contribution Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbr

A global biopharma company is looking for a Senior Manager, Clinical Trial Study Start-Up, to lead study start-up activities from site identification to activation.

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. This position combines people leadership with operational excellence, driving consisten

The Senior Manager, Clinical Trial Study Start‑Up is a subject matter expert in clinical study start‑up and is responsible for leading the process that enables planning, coordination, and execution of study, country and site‑level start‑up activities from site identification through to site

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

We are currently looking for a Trial Vendor Senior Manager to join our team. As a Core member of the Clinical Trial Team (CTT) you will independently manage all vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance st

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

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. You’ll have experience as an Account Manager within an agency working on healthcare accounts. Langland, a

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

Support set‑up, maintenance, closeout and archiving of the Trial Master File (TMF), ensuring continual inspection readiness. Minimum of 3‑4 years of progressive clinical trial experience. The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and

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.

A leading health communications agency in Greater London is seeking an ambitious Account Manager to manage client accounts effectively.

A pharmaceutical company in the United Kingdom is seeking a Clinical Trial Manager to oversee all aspects of clinical trial management for global studies, ensuring compliance with regulatory standards. The ideal candidate will have a bachelor’s degree in a related field and over 5 years of experie

A prominent health communications agency in Greater London is seeking an Account Manager to oversee client accounts.

Together, Inclusive and TrialEngine form the only end‑to‑end platform to automate the back office of clinical trials, from pretrial to trial close. Partnerships Manager (Clinical Trial, SaaS, Health tech). Our mission is to enable faster, more successful clinical trials by engineering smart soft

R&D Partners is seeking a Clinical Trial Manager to lead the design, planning, execution, and oversight of global clinical studies for the Renal Denervation portfolio. Lead global innovation in renal care by steering high‑impact clinical trials from concept to completion. The ideal candidate will

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.

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. You’ll have experience as an Account Manager within an agency working on healthcare accounts. Langland, a

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. Develop and manage clinical trial supply plans to meet project timelines and requirements. Collaborate w

A leading biopharmaceutical company is seeking a Global Study Manager for an interim remote position. 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. Experience with clinical trial submissions via CTIS and coordination with Ethics Committees and

Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbridge. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxbridge. Assist in training for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs).

A leading dermatology company based in London is seeking a Clinical Trial Associate Manager to ensure successful execution of clinical trials. The role involves overseeing a team of Clinical Trial Associates, ensuring compliance with ICH-GCP and regulatory requirements.

We are currently looking for a Trial Vendor Senior Manager to join our team. As a Core member of the Clinical Trial Team (CTT) you will independently managing all vendor-related aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance

A leading clinical research organization based in London is seeking an Associate Clinical Trial Manager to join their team.

A leading healthcare communications agency in Greater London is seeking an Account Manager to oversee the management of key client accounts.

Single Sponsor European Clinical Trial Manager. As a P22 level Clinical Trial Manager, you will oversee the development, coordination, and implementation of Phase I‑IV studies, ensuring milestones, budgets, and regulatory compliance while collaborating with principal investigators and cross‑func

A leading biopharmaceutical solutions organization is looking for a Single Sponsor European Clinical Trial Manager to coordinate Phase III clinical research studies across Europe.

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##

An educational institution in London is looking for a Trial Manager to coordinate the ‘GP‑TEST‑PRO’ cancer screening trial. The successful candidate will manage participant recruitment, oversee trial timelines, budget adherence, and ensure compliance to regulations.

A leading biopharmaceutical solutions organization is seeking a Clinical Trial Manager to oversee Phase III studies across Europe.

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

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. You'll partner with Project Managers and lead client meetings to drive success, all while enjoying fantastic benefits tha

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. Communicate and collaborate on global study activities; working clo

Impact and Contribution: Roles within the Clinical Trial Management job family at the P22 level significantly impact the success of clinical trials by ensuring that all aspects of the study are meticulously planned and executed. Single Sponsor European Clinical Trial Manager - 2-3 days a week in Uxb

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. Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Ensures compliance of clinical trials with national and international regulatory requirements and co‑monitors the assigned

You will work closely with project managers (central and/or specialty labs) and lend expertise to clinical trial management (CTM) and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries. Parexel are currently recruiting for an experienced C

Finance Manager - £45k - £50k per annum - Full time - Permanent - Greater Exeter.

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. Webelievethat people are the most valuable asset of any clinical trial. We partner with our clients across t

Parexel International is seeking an experienced Clinical Trial Manager (CTM) to join their team in the UK, dedicated to managing individual clinical trials. Preferably, candidates will have experience in oncology or CNS trials.