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Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis) Are you an experienced Vendor Management professional looking to make an impact in global clinical trials? We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor Department, dedicated exclusively to Novartis. In this role, you 'll become an expert in Vendor Management for global clinical trials across all phases (Phase I–IV), ensuring seamless execution from study start-up through close-out. What We’re Looking For To excel in this role, you should bring: • Global Clinical Project Management experience, • Strong Vendor Management expertise: Central lab, eCOA, IRT, ECG, Imaging, Ancillaries and/or Patient Recruitment & Retention with experience in global clinical trials. (must have experience managing at least 2 of these vendors), • Deep understanding of clinical operations processes and vendor service categories., • Excellent project management skills to drive efficiency and collaboration, • Strong communication and influencing abilities to partner effectively across functions., • Proven ability to manage risk and performance issues in a fast-paced environment What You’ll Do As a Global Clinical Project Manager - Vendor Management Expert, you will be responsible for ensuring vendor deliverables are met with quality and efficiency at the trial level. Your key responsibilities include: • Vendor Oversight & Coordination – Manage vendor activities across the study lifecycle, ensuring timely and high-quality deliverables., • Study Start-Up Support – Oversee vendor deliverables during study initiation, ensuring smooth onboarding and activation., • Risk & Performance Management – Track vendor performance, identify risks, and escalate issues as needed., • Site Readiness & Activation – Drive vendor activities to support site activations and ensure study milestones are met., • Study Close-Out – Coordinate vendor deliverables that support Database Lock and study closure. What You’ll Deliver • Vendor service excellence at the study level, • Vendor onboarding and performance tracking, • KPI (Key Performance Indicator) and KQI (Key Quality Indicator) dashboards to monitor vendor effectiveness, • Site readiness monitoring and documentation, • Risk mapping with contingency planning, • Vendor cost control and oversight Please note this role is not eligible for the UK visa sponsorship. This is an exciting opportunity to play a critical role in global clinical trials, ensuring vendor excellence and operational success. If you’re ready to take on a high-impact role with a leading sponsor, we’d love to hear from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ___ IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. Work as the primary Point of contact for the customer project manager. Support professional de

Global Trial Delivery Manager services provide for the global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure global clinical operations deliverables progress according to agreed upon timelines and milestones, including country & site feasibility and site selection, trial set-up, trial execution and trial closure and vendor set up activities as assigned by the Global Clinical Development Operations Trial Leader (GTL). This service supports the GTL in leading related CRO, country, and site activities, including global vendors involved in site facing activities such as IVRS, Central Lab, ePRO, Imaging, Translation, Printing, Ancillary supplies and Meeting Planners. Interface with stakeholders; internal and external to Global Clinical Development Operations (GCDO) functions, such as Study Responsible Physician, Global Data Manager, Trial Supply Manager, CRO staff, vendor staff and trial sites (if applicable). Work closely with the GCDO Trial Leader (GTL) and is member of the Trial Team, led by the GTL. Ensure inspection readiness through compliance with the clinical research protocol, company Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through close-out. Takes ownership for assigned responsibilities. Demonstrated competency to act as a backup or first point of contact in absence of the GCDO Trial Leader. Advanced is given assignments that are more complex and/or have a greater potential impact on business results. May act as the lead over a team of CTMs across a project/program, on insourced and outsourced studies. Able to lead taskforces and provide innovative input. May contribute to process improvement and/or non-project work. Task: • Services rendered will adhere to applicable to sponsor´s SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc., • Complies with relevant training requirements., • Lead the Study Management Team including providing updates to all trial team members on deliverable status., • Ensure availability of required reports to support real time tracking of trial status according to trial plan., • Manage timely and accurate documentation and communication of trial progress., • Ensure that the Study Management Team (SMT) operates in a constant state of inspection-readiness., • Act as primary contact for Country and Regional staff., • Act as the primary contact person for the local teams within GCDO., • Partner with the Global Trial Lead to execute and oversee central activities from planning, trial start up, through the life of trial to close-out., • Ensure issue escalation and drive issue resolution., • Work closely with Trial Team to ensure CAPAs are resolved timely. Act as CAPA owner or contributor, as appropriate., • Contribute to data collection to support the site selection process., • Participate in feasibility, providing recommendations as needed., • Establish enrollment commitments and ensure actual enrollment meets projected commitments across the regions at the clinical trial level., • Ensure the availability of robust recruitment/contingency plans are in place for each region., • Ensure timely tracking and filing in appropriate systems, as required at central trial oversight level., • Perform Annual Quality Review of files, as appropriate., • Ensure archiving and retention of documents per set requirements., • Establish country budgets and monitor actuals vs. forecast for Out-of-Pocket Expenses., • Oversight of selected vendors and status of related deliverables., • Review and approve assigned vendor invoices/spend., • Monitor budgets and expenditures as expected per planned trial budget., • Create and update trial-specific documents as required, including Monitoring Guidelines, Informed Consent Form, Investigational Medicinal product (IMP) related documentation, Blinding Plan, country and site feasibility related documents., • Provide input into cross functional documents such as safety related documents, protocol deviations and issue escalation processes, External Service Provider Oversight Plan and the Filing and Archiving Plan., • Provide central documents required for HA/EC/IRB submission., • Ensures creation of appropriate trial-specific training materials and requirements, making them available to the regional/site/CRO staff and delivering training as needed., • Responsible for the set-up, coordination, attendance participation of Investigator Meetings., • Establish and maintain excellent working relationships with internal stakeholders, such as country representatives, data management leader and clinical supplies unit., • Demonstrate deep knowledge of protocol and procedures and adequate therapeutic area knowledge., • Ensure compliance with Health Authority regulations and guidelines and internal standard operating procedures and processes., • Participate in preparation for, and conduct of, Health Authority inspections and internal audits., • Work with Bioresearch Quality & Compliance (BRQC) liaisons to ensure quality oversight of assigned trial utilizing the available tools., • Coordinate data cleaning with some supervision towards a timely and successful database lock., • Act as central expert for assigned protocol(s)., • Sufficient therapeutic knowledge to support defined CTM roles and responsibilities., • Contribute to process improvement and training, as applicable. Requirements: • BS degree or equivalent, in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy)., • 6-8 years clinical trial management experience in the pharmaceutical industry or CRO. Specific therapeutic area experience., • Strong working knowledge of ICH-GCP, local laws and regulations., • Superior clinical research operational knowledge. Proven track record in successfully managing various aspects of trials from start-up to database lock and trial closure., • Demonstrated effective leadership to proactively drive the Study Management Team through key stages of trials, as well as delegation skills., • Effective leadership skills and ability to manage multiple stakeholders., • Proven ability to lead a team through formation stages, up to operating as a high performing team., • Experience and ability in coordinating global or regional teams in a virtual environment. Proven ability to foster team productivity and cohesiveness., • Experience and ability in coordinating global teams in a virtual environment for a minimum of 2, preferably 3 years., • Proven experience in proactive planning, risk mitigating and gaining team consensus on updated plans during the project lifecycle., • Strong project planning/management., • Independent complex decision making., • Solution oriented and proactive risk identification and mitigation., • Strong IT skills, including knowledge of standard Microsoft applications, Trial Master File, Clinical Trial Management System, and willingness to learn new systems., • Monitoring experience is recommended, or other relevant experience should be considered, such as data management or central monitoring., • Travel., • Proficient in speaking and writing local country language and English., • Effective verbal and written communication skills leading to successful team collaboration, • Strong decision making. Solution oriented., • Strong analytical skills, and simultaneously demonstrates the ability to manage ambiguity when limited information is available., • Experience in developing presentations and presenting key information to stakeholders., • Ability to understand and competently plan and have oversight of country and select vendor budgeting processes, i.e. Understand and be aware of country Out of Pockets (OOPs) and FTE cost drivers. *Please note This role is not eligible for UK visa sponsorship IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ___. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

Clinical Operations Program Manager – Single Sponsor (Novartis) Are you a clinical operations professional with a passion for feasibility and strategic planning in global trials? We are seeking a Clinical Operations Program Manager (Global Feasibility Lead) to join our Single Sponsor Department, dedicated exclusively to Novartis. In this role, you will lead early viability, feasibility, allocation, and site selection activities to support global clinical development programs. What We’re Looking For To thrive in this role, you should bring: ✅ 4–5 years of global feasibility experience in clinical trials ✅ Strong analytical and strategic planning skills, including scenario planning and risk management ✅ Excellent communication and stakeholder engagement abilities ✅ Proficiency in feasibility dashboards and data-driven decision-making ✅ Fluency in English and a Bachelor’s degree in Life Sciences ✅ Excel expertise, ability to analyse data in large databases What You’ll Do As a Clinical Operations Program Manager, you will drive end-to-end feasibility and strategic allocation planning across global trials. Your key responsibilities include: Feasibility Leadership – Conduct early viability, pre-IMB, and trial-level feasibility assessments. Lead survey analysis and consolidate insights to inform site selection. Strategic Allocation & Scenario Planning – Validate allocation strategies using internal/external data and tools like Footprint Optimizer (FPO). Develop evidence-based timelines and risk mitigation plans. Stakeholder Engagement – Prepare briefing materials, training resources, and coordinate cross-functional meetings. Track actions and deliverables. Portfolio & Risk Management – Support portfolio tracking, tollgate reviews, and risk presentations. Draft SPF overviews and ensure compliance with internal systems (e.g., IMPACT, CREDI/Subway). Operational Excellence – Manage feasibility documentation, pricing assumptions, and logistics for team meetings. Ensure quality handover to study teams. What You’ll Deliver Feasibility excellence across global trials Data-driven allocation and site selection strategies Scenario planning and risk mitigation outputs Stakeholder-ready dashboards and briefings Compliance with internal systems and documentation standards This is an exciting opportunity to play a critical role in shaping global clinical trial strategy. If you're ready to bring your feasibility expertise to a high-impact role with a leading sponsor, we’d love to hear from you! Please note this role is not eligible for the UK visa sponsorship. Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered . IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ___ IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Interface with stakeholders; internal and external to Global Clinical Development Operations (GCDO) functions, such as Study Responsible Physician, Global Data Manager, Trial Supply Manager, CRO staff, vendor staff and trial sites (if applicable). Collaboration - Ability to establish and maintain ef

Senior Global Trial Manager – Single Sponsor (Novartis) Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global Trial Manager to join our Single Sponsor Department, dedicated exclusively to Novartis. Join our global team and take ownership of delivering late-phase clinical trials that meet timelines, budgets, and quality standards. As a core Clinical Trial Team (CTT) member, you'll lead critical aspects of global studies and collaborate across functions to drive success. As part of your role, you’ll have the opportunity to specialise in one for the following areas: · Scientific Review Committee (SRC) · Non-Interventional Studies (NIS) · Managed Access Programs (MAP) · Investigator-Initiated Trials (IITs) · Research Collaborations (RCs) · Program Level Documents (PLD) Key Responsibilities: Clinical Documentation & Study Tools · Draft sections of protocols, CRFs, training materials, and data review plans · Contribute to the development of safety updates, IBs, and regulatory submissions Project Leadership · Oversee data review and TMF audit readiness · Forecast/manage investigational product supply · Support study closeout, issue resolution, and lifecycle budget tracking · Contribute to Managed Access Program coordination and compliance Vendor & Stakeholder Management · Coordinate CRO/vendor selection and performance · Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison · Lead cross-functional collaboration with data management, drug supply, and more What You'll Bring · Advanced degree in life sciences or healthcare · 2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials · Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports) · Excellent communication, organizational, and collaboration skills · Deep understanding of GCP and clinical trial design · Passion for advancing real-world evidence and patient outcomes This role is not eligible for UK VISA sponsorhip. IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ___. At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes.

Job overview As a Vendor Lead you will be a Single Point of Contact (SPOC) for supplier services at a trial level and be the first point for issue escalation during study start up, acting as a conduit for clear communication and robust daily oversight Main responsibilities * Maintain close interaction and collaboration with study team lead and study team members during study lifetime * Review of the vendor and category related specific sections of the protocol, ensure vendor expertise is leveraged when refining specifications towards Final Protocol * Ensure changes to protocol or study designs are consistently shared with vendors and incorporated into supplier budgets, timelines, and specifications. * Contribute to development of Study Specification Worksheet (SSW) to facilitate bid process and selection of Vendors. * Quote/Proposal review in collaboration with procurement (and vendor). If required, support contract negotiations. * Vendor budget review of final quotes * Co-ordinate vendor kick-off meeting and other vendor specific meetings * Collect HA submission documents from vendor, as requested by countries participating in a study * Support amendment of vendor contracts with Procurement team * Optimise a frontloaded and timely study start-up process in support of a timely vendor DB-go-live * Pro-actively create and maintains vendor related risk maps with contingency plan for documentation For eCOA vendor manager: * Responsible for directing the vendor on the specific study requirements for system set up and leading the design, build, testing and validation of the system (UAT) * Collaborate with the Study Lead, External Relationship Lead, Procurement, and the Quality Assurance teams (QA) to assure the set up and delivery of ECOA supplier providers Qualifications * Bachelor's Degree Bachelor's Degree in health care or other scientific discipline required * Excellent communication skills. * Communication - Strong written and verbal communication skills including good command of English language. * Previous experience in: vendor management, system design, demand & contracting process. * Expertise with one of these vendors are required: eCOA, IRT, Central lab, Patient Recruitment and Retention This position is not eligible for UK VISA Sponsorship IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at ___ IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Job Title – Receptionist Location – Reading Hours – 40 hours per week and flexible to work weekends Salary- £25,400 Optical Express is the UK’s only complete eye care provider, and Europe’s leading private provider of laser eye surgery and premium intraocular lens and cataract surgery. Each week Optical Express Surgeons undertake more laser eye surgery and private intraocular lens procedures collectively than any other providers. For over 35 years, millions of patients have trusted Optical Express with their eye care. Operating clinics across the UK, Ireland, and mainland Europe, Optical Express, supported by an esteemed International Medical Advisory Board, is a thought leader in the global optometry and refractive surgery industry. Optical Express gives patients their very best results through investing in state of the art technology, employing experienced, highly skilled surgeons and optometrists, continuously analysing clinical outcomes and working with pioneers and innovators from within the industry, to include Johnson & Johnson Vision and Zeiss. You will work as part of a team providing a high level of service to the patients and employees and will require the ability to multi-task in a busy retail environment. This role is a key part of the patient journey and requires very high personal standards to deliver a quality of care and world class customer experience. Every day will bring something new but your day to day role will involve • Covering the reception area, maintaining a priority for incoming calls at all times, • Take clear and concise messages, • Communicating all messages promptly and accurately, • Provide administrative support to the Manager, • Maintain stationery stocks and oversee the ordering of new supplies, • General reception duties as and when required This is a dual role covering both the Reception desk and Surgery. Following appropriate training, supervised practice and competency achievement assessments, you will be able to undertake all designated roles within the surgery team working across two surgical specialities: laser vision correction department (LVC) and ophthalmic (IOL) theatres. We are looking for applicants who are confident and professional, who have a passion for providing a world class customer service along with strong organisational and communication skills. You will have the ability to work closely with others around you, be articulate and presentable, motivated to achieve and have a willingness to learn and progress within Optical Express, whilst demonstrating confidentiality, integrity and discretion at all times. What’s in it for you? • Free or discounted optical products/procedures, • Career progression, • Modern working environment with superb technology support Please apply now by uploading your CV. This is a fantastic opportunity to join a global organisation where you will have the opportunity to grow and develop within a professional working environment. Optical Express is an equal opportunities employer

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis) Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor De

Project Manager – Clinical Supply Services – Pharmaceutical sector.Are you organised, detail-oriented, and passionate about delivering critical healthcare solutions? Do you enjoy coordinating complex processes and working with international teams? Do you have experience in the pharmaceutical sec

Efficiently managing multiple teams on EPR delivery. Senior Technical EPR Delivery Manager. EPR, Technical Delivery, Documentation, Testing, Clinical Applications, People Management, Agile.

Senior Global Trial Manager – Single Sponsor (Novartis) Are you experienced in managing late phase clinical trials at a global level? We are looking for a Senior Global Trial Manager to join our Single Sponsor Department, dedicated exclusively to Novartis.

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis).Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?.Global Clinical Project Manager - Vendor Management Expert.In this role, you 'll become an expert in

Senior Project Manager- Clinical Software Fully remote with some travel to NHS Trusts in the UK As a Senior Project Manager- Clinical Software you will manage a portfolio of projects with a selection of key clients. Role responsibilities for the Senior Project Manager- Clinical Software: * Project

The Company Nurse Manager will have responsibility for providing clinical and commercial leadership to a team of Stoma Care Nurses in the UK Ostomy Business, consistent with the Companies’ mission and vision. Other projects and duties as assigned by Clinical Nurse Director. The position holder wil

The Patient Support Operations Manager (Digital Clinic) plays a pivotal role in managing the daily operations of Montu's clinical services and the Patient Support Coordinator team. Supervising, mentoring, and supporting the Patient Support Coordinator team to ensure the smooth day-to-day running of

Global Clinical Project Manager - Vendor Management Expert. Strong Vendor Management expertise:. Vendor Oversight & Coordination.

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As Care Home Deputy Manager & Clinical Lead of Oulton Park care home in Lowestoft, you'll support the delivery of the quality care we're known for. To join us as a Care Home Deputy Manager & Clinical Lead, you'll need be a Registered Nurse (RN/RMN) with current NMC registration and a teaching/mentor

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An exciting opportunity to join Veramed's Data Management Business Unit! As we continue to grow and build on our success, we're looking to recruit a passionate and driven Senior Clinical Data Manager. The role of the Senior Clinical Data Manager is to provide data management support to the data mana

Minimum of 5 years post-qualification in your clinical profession. Current clinical registration (e. Castlefield is proud to be partnering with a well-established Case Management company operating within the Medico-Legal sector to recruit an experienced Case Manager.

This field-based role reports to the Clinical Business Manager and requires a proven track record of successfully managing clinical teams and delivering results in complex healthcare settings. Clinical Nurse Manager - South East. We are looking for an experienced Nurse Manager to lead the Homecare

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis) Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor De

Clinical Operations Program Manager – Single Sponsor (Novartis)Are you a clinical operations professional with a passion for feasibility and strategic planning in global trials?We are seeking a Clinical Operations Program Manager (Global Feasibility Lead) to join our Single Sponsor Department, ded

Clinical Operations Program Manager – Single Sponsor (Novartis)Are you a clinical operations professional with a passion for feasibility and strategic planning in global trials?We are seeking a Clinical Operations Program Manager (Global Feasibility Lead) to join our Single Sponsor Department, ded

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis) Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?We are seeking a Global Clini

Clinical Practice ManagerHome-based (with regular regional and occasional national travel)About UsAt Family Action, we transform lives by providing practical, emotional and financial support to those experiencing poverty, disadvantage and social isolation.

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

Clinical Nurse Manager Deputy ManagerWhen registering to this job board you will be redirected to the online application form. Position:Clinical Nurse Manager - Deputy ManagerCare home: Tees Grange Location: Norton, Stockton-on-Tees, TS20 2PHContract type: Monday - Friday (40 hours per week)Rate: £

Freelance Clinical Project Manager. Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements. Proven ability to work independently and manage global clinical operations.

Deputy General Manager (RN)- Care HomeLocation: Trowbridge, Wiltshire,BA14 9ENHours: 40 hours per week (Including some shift work)Pay: £55,000 per annumThe Role:Support the General Manager and lead the home in their absenceOversee care standards through audits, clinical supervision, and compliance

Freelance Clinical Project Manager. Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements. Proven ability to work independently and manage global clinical operations.

Are you a skilled Clinical Deputy Manager looking for your next challenge? Our client, a boutique provider of UK care homes, is seeking a Clinical Deputy Manager to join their team at a care home in Exeter. This role offers an exciting opportunity to lead and develop clinical care teams and comes wi

This position is responsible for creating and maintaining supply strategies for investigational products across global clinical studies. The role requires proactive collaboration, strategic planning, and operational excellence to ensure timely delivery of quality clinical supplies while navigating c

The team at Salisbury Manor Care Home have a great opportunity for a passionate and hands on nurse to join the home as clinical deputy manager. What youll doSupporting and deputizing for the Home Manager, you w.

The Global Study Manager is responsible for supporting the delivery of clinical studies ensuring quality and compliance. Minimum of 3-4 years of progressive clinical trial experience. The exact accountabilities will differ depending on the exact nature of the clinical program, so a high degree of fl

We are currently looking for an experienced and motivatedClinical Registered Managerto lead Our Hazlemere Lodge Care Home in High Wycombe, a 64-bed residential service. As the Clinical Registered manager at Hazlemere Lodge Care Home, youll be at the heart of delivering exceptional, perso.

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Job Title:PHB Specialist clinical ManagerReports To:Chief Operating OfficerLocation:TelfordSalary:£50,000 - £60,000 Per AnnumHours:Full-time (37. Job Purpose:To lead the development and delivery of a specialist Personal Health Budget (PHB) service that supports Integrated Care Boards (ICBs) in sel

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Location: TelfordSalary: Competitive Job Type: Full-time, PermanentReports to: Senior Leadership TeamAbout the RoleKomplex Community is seeking two passionate and experienced Clinical Nurse Managers (RMN and RNLD) to lead a caseload of clients with mental health needs, learning disabilities, and aut

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This is a great opportunity for a passionate and hands on nurse to join the home as a clinical deputy manager.

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Are you ready to step into a leadership role as a Deputy Manager? Our client is looking for a dynamic individual to support the Registered Manager in overseeing various functions such as care, administration, and maintenance. With an annual salary of £60,000, this Deputy Manager role offers you the

Global Clinical Project Manager - Vendor Management Expert – Single Sponsor (Novartis) Are you an experienced Vendor Management professional looking to make an impact in global clinical trials?We are seeking a Global Clinical Project Manager - Vendor Management Expert to join our Single Sponsor De

Ensure compliance of clinical trials with national and international regulatory requirements and co-monitoring the assigned clinical trial following company SOPsEnsures the study is “inspection ready” alwaysResponsible for oversight and coaching of the f