• Upfront support of Medical Device clinical trials and research, supporting statistical aspects of study design by assisting with sample size calculation via power analysis and study design, and ensuring the protocol and variables collected support the endpoint analysis. • Execute statistical analyses including, but not limited to, established methods such as confidence interval testing, regression models, Bayesian methods, missing data handling, mixed models. • Create reproducible code, summary tables, visualizations, and written statistical outputs that support study reports, technical documents, and defend results to regulatory agencies. • Prepare analysis datasets by performing data cleaning, validation, formatting, and code reviews. • Document statistical approaches and analytical workflows to promote transparency and reproducibility to be documented in the Clinical History File. • Collaborate with cross‑functional partners including Clinical Operations, Quality and Regulatory, engineering, and data management teams to support project execution.

Role Description We’re supporting a leading UK healthcare provider in recruiting an NMC-registered Clinical Homecare Nurse to deliver high-quality patient care across South Wales. This role suits a confident, compassionate nurse who thrives working independently in community settings, providing safe and effective treatment for patients outside of hospital environments. As demand for home-based care continues to grow, Clinical Homecare Nurses are central to ensuring patients receive professional, consistent, and compassionate support where they live or work. You’ll visit patients in their homes, schools, or community settings to administer prescribed treatments, monitor progress, and promote independence in managing their care. You’ll combine clinical excellence with strong communication skills, ensuring every patient receives a safe, positive, and reassuring experience. Key Responsibilities - Conduct clinical assessments and ensure patients are fit to proceed with treatment - Administer medications and therapies (S/C, IM, IV) as prescribed - Monitor vital signs and escalate clinical concerns appropriately - Educate and support patients and their families to improve understanding and confidence in their treatment - Maintain accurate clinical documentation in line with governance standards - Work collaboratively with multidisciplinary teams to ensure patient safety and continuity of care Qualifications - Current NMC registration (Adult) - Proven experience administering S/C, IM or IV medications - SACT experience desirable - Full UK driving licence - Comfortable working autonomously and managing a regional caseload - Excellent clinical standards, attention to detail, and patient focus Benefits - Competitive salary: £35,000–£38,000 (DOE) - Company car and mileage reimbursement - 33 days annual leave (including bank holidays) - Annual company bonus scheme (subject to eligibility) - Pension scheme (auto-enrolment with employer contribution) - Private medical insurance and life assurance - Access to Employee Assistance Programme, counselling, and virtual GP services - NMC fee reimbursement - Uniform provided - Ongoing professional training and revalidation support - Opportunity for SACT training and assessment Apply Now If you’re an experienced clinical homecare nurse looking for autonomy, patient connection, and professional growth, we’d like to hear from you.

• Handles all aspects of contract administration, specifically related to third-party awards in support of NMDP's research efforts. • Presents business strategies, agreements, subcontracts, grants and third-party awards to internal stakeholders to determine accurate contracting arrangements for research projects. • Prepares and reviews contractual documentation for third-party award submissions, both government and non-government; creates appropriate flow down terms and conditions for each award to be applied to future agreements. • Provides oversight to ensure that the EEO, FAR, OMB and related Federal requirements are incorporated, as required, into individual subcontracts/sub-agreements/purchase orders. • Assists with the preparation, negotiation, and maintenance of third-party awards by collaborating with internal partners to ensure deadlines are met, documents are updated, and projects are being conducted in accordance with any applicable agreement/award terms and conditions. • Supports NMDP's study networks (CIBMTR, BMT CTN, PTCTC) by negotiating and overseeing contracts throughout the life of a clinical trial; attends regular meetings to receive and provide updates on clinical trials. This role will be expected to provide contractual support to many aspects of a clinical trial, including funding agreements, laboratory agreements, clinical trial agreements, study riders, along with other contracts as required by the protocol or study team. • Advises key stakeholders about the legal and regulatory environment; identifies special arrangements, provisions, or legal/business requirements of the solicitation; defines and establishes agreements with third parties, including subcontractors. • Oversees or conducts negotiation of contracts and third-party awards; documenting discussions and using sound judgment and seeking the appropriate management approval for the acceptance of legal, financial and operational terms and conditions. • Safeguards NMDP’s intellectual property (IP) assets by using appropriate patent, trademarks, trade secret, and technical data/software agreements and provisions. • Develop, implement or modify Standard Operating Procedures (SOP) for contract management and administration in compliance with company policy. • As appropriate, contribute to or influence company policy. • Maintains contractual records and documentation and monitors compliance of established contract with internal stakeholders with established procedures. Responsible for the input and accuracy of procurement and contracting documents in an electronic database. • Conducts business with integrity, upholding high ethical standards in full accordance with contract requirements. • As needed, provides guidance on contract matters to internal stakeholders including training in contracting practices and procedures. • This role may focus on one or more of the following areas: procurement, contract support and prime contract/grant management.

• The Study Operations Manager I (SOM I) has responsibilities for study and regional or specific country level activities from study startup through conduct and study close on one or more studies, providing leadership, strategic planning, and organization skills to ensure the operational delivery of tasks. • Supports Global Study Managers (GSMs), other SOMs, and the larger study management delivery of the study by leading specific parts of the project, driving specific countries, executing tasks of moderate complexity, and developing solutions to problems as needed to support deliverables • Serves as leader of the local study team (core members, ad hoc members, and other key stakeholders as required) on one or more studies • Oversees the preferred Contract Research Organization (pCRO) and/or Country Trial Manager (CTM)/Site Care Partner (SCP) for assigned studies at country level in accordance with the overall project plan, and manages and maintains accurate country level plans (e.g., timelines, budget, risk, and quality plans) • May manage the study start-up process in countries assigned [where the Start Up Project Manager (SUPM) is not assigned] and/or oversee the pCRO responsible for these activities as applicable • Liaises with SCP, Lead SCP, Site Activation Partners (SAPs), and regulatory colleagues in country to agree on submission strategy to Health Authorities (HAs) and Ethic Committees (ECs) • Provides country level input on startup and recruitment milestones as provided by pCRO and/or CTM/SCP to GSM during planning • Collaborates with accountable roles to identify and manage deviations and risks in study startup and execution and implements mitigation strategies as required. • Accountable for resolution of site activation escalations to study teams including offering options for mitigation • May be responsible and accountable for, as designated by the GSM: Regional, country and study level recruitment strategy • Communication with the local team and internal stakeholders and pCRO as applicable to ensure efficient and timely study delivery of the agreed plans • Study and/or country vendor management and oversight including follow up and coordination of vendor deliverables • Assurance of the follow up and coordination of regional and site quality events, protocol deviations, data issues, metrics review, site issues and risks, audit responses, etc. • Acts as the point of contact for all study level questions for the local study team, ensuring resolution at lowest possible level, and when needed liaising with and escalating to appropriate global roles and teams • May lead operational effectiveness initiatives at country or regional level • Utilizes roles in country such as Lead SCP, and expert roles such as Contracts Leads and SAPs, to provide the global teams with local intelligence and operational nuances to be considered • Provides input on country level per subject costs, local vendor costs, and other fees where applicable • Utilizes country intelligence to provide input on country specific risks into preparation of Investigational Quality Management Plan and Study Monitoring Plan, and ensures Trial Master File (TMF) completeness and oversight of all relevant compliance activities for allocated studies • Supports implementation of client’s site technology experience systems • Supports implementation of new tools and technologies (e.g., eConsent, eISF, remote source access, remote source data verification/review (SDV/SDR), iConnect, implementation of protocol required decentralized trial options)