• Collaborate with cross-functional teams, including Clinical Operations, Medical Affairs, Biostatistics, and Regulatory Affairs, to design scientifically rigorous late stage clinical trials. • Contribute to the development of study protocols, investigator brochures, informed consent forms, and other essential study documents. • Provide scientific input for trial endpoints, patient populations, and statistical analyses. • Act as the scientific lead for assigned late stage studies, ensuring adherence to clinical trial protocols and regulatory requirements. • Provide ongoing scientific and clinical input during trial execution, including participation in investigator meetings, site initiation visits, study monitoring activities, and medical data review. • Review and interpret clinical trial data, ensuring consistency and alignment with study objectives. • Address protocol-related questions from investigators and site staff. • Contribute to the preparation of regulatory submissions, including clinical study reports (CSRs) and documentation for Investigational New Drug (IND) and New Drug Application (NDA) filings. • Ensure clinical trial activities are conducted in compliance with Good Clinical Practice (GCP) guidelines and applicable regulatory standards. • Collaborate with the Biostatistics and Data Management teams to review and interpret study data, ensuring accuracy and completeness. • Participate in the preparation of abstracts, presentations, clinical study reports, and manuscripts for scientific meetings and publications. • Partner with cross functional team members to develop and execute clinical development strategies. • Serve as a subject matter expert within the clinical team, providing scientific insights to support decision-making.

• 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.