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ABOUT THE ROLE This is a casual, part-time role offering flexible working. As a Bank Registered Nurse at a Barchester care home, you'll look after the physical, psychological and social needs of our residents to help us deliver the quality care they deserve. We'll look to you to create a safe and supportive environment for residents with range of physical and mental needs, whilst also relying on your professional judgement to make critical clinical decisions. You can expect a wide range of responsibilities, from developing tailored care plans to providing medicine safely and delivering excellence across everything you do. As a Registered Nurse (RGN), you'll have the freedom and autonomy to do things the right way and be truly valued and respected for what you do. ABOUT YOU You'll need to have current NMC registration and a good knowledge of the most up-to-date clinical practices to join us as a Registered Nurse (RGN). Experience of producing well-developed care plans and detailed risk assessments is important too, as is an understanding of regulatory frameworks, including DoLs/MCA and Royal Pharmaceutical guidelines. Dedicated and compassionate, you'll pride yourself on your person-centred, thoughtful approach to nursing. REWARDS PACKAGE As well as competitive pay, you can look forward to a role that offers true flexibility and plenty of free learning and development opportunities. As one of the UK's leading healthcare providers, we take the growth of everyone who works for us seriously. As this is a Bank position to provide cover as and when we need it, such as for annual leave or sick leave, the hours and days you work will vary. If you'd like to use your clinical and people skills in an organisation that provides the quality care you'd expect for your loved ones, this is a rewarding and empowering place to be. #2003

Apply Now!! through MYN!! Take the next step in your specialist career and come and experience the best of Belfast and Northern Ireland. MYN is looking for you! • Nuclear Medicine Radiographers, • MRI/CT Radiographers, • Mammographers, • Sonographers Employer: Leading Hospital in Belfast (represented by MYN) Directorate: Surgical & Clinical Services Division Location: Belfast (Trust wide across multiple hospital sites) Hours: Full Time (37.5 hours per week) Contract: Permanent Salary: £36K – £53K per annum The Opportunity We are looking for a passionate and skilled Nuclear Medicine Radiographer to join a forward thinking and patient centred team. You will play a pivotal role in delivering high quality diagnostic imaging services. This role offers a fantastic opportunity to develop your skills across a wide range of nuclear medicine procedures in a well equipped and supportive department. You will participate in extended working days and out of hours sessions, including general X ray rotation and on call responsibilities, contributing to a responsive and comprehensive service. Main Responsibilities • Clinical Excellence, • Perform a wide range of nuclear medicine duties, including radionuclide imaging, organ uptake measurements, and quantitative analysis of imaging data., • Prepare and dispense radiopharmaceuticals, ensuring the highest standards of safety and accuracy., • Prepare imaging data for clinical reporting and ensure all clinical data is securely archived according to departmental protocols., • Champion patient care by maintaining the highest standards of compassion, communication, and safety, with a special focus on radiation protection and dosage., • Strictly adhere to all Radiation Protection rules, including IR(ME)R 2018 NI, Ionising Radiation Regulations 2017, and Local Rules., • Take responsibility for the safe and effective use of equipment, promptly reporting any defects or safety concerns., • Leadership, Mentorship & Development, • Lead by example, setting a high standard of personal and professional conduct within the team., • Provide guidance, support, and clinical supervision to junior staff, assistant practitioners, and student radiographers, contributing to a positive learning environment., • Actively participate in research, clinical audit programmes, and the evaluation of new procedures and equipment to drive continuous improvement., • Commit to your own continuing professional development (CPD) through post registration courses and in service education., • Service Contribution & Flexibility, • Participate fully in the departmental rota, including extended working days, evenings, weekends, public holidays, and the emergency out of hours service (including at short notice)., • Contribute to the general X ray rotation and on call services as required, demonstrating flexibility to meet the evolving needs of the service. Essential Qualifications: HCPC/CORU Registration as a Diagnostic Radiographer. A recognised qualification in Nuclear Medicine (Desirable). Knowledge: Related Diagnostic Radiography principles and best practices. A thorough understanding of IR(ME)R 2018 NI, Ionising Radiation Regulations 2017, and their practical application. of radiation protection principles and local rules Minimum 1 Year relevant experience Skills: Excellent communication and interpersonal skills, with the ability to work both autonomously and as part of a multidisciplinary team. A commitment to delivering compassionate patient care and evidence based practice. Values: A demonstrable commitment to the HSC values: Working Together, Excellence, Openness & Honesty, and Compassion. Additional Information This appointment is subject to a successful pre employment checks and health assessment. Candidates must have the right to work in the ROI or UK. A 6 month probationary period applies.

ARC's purpose is to expedite access to precision medicine clinical trials for patients globally. We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and the important relationships we have developed with our global clients. We are a Belfast-based Clinical Research Organisation that specialises in delivering compliance excellence for companies in the precision medicine sector. We support many of the world's leading pharmaceutical R&D companies in implementing unapproved diagnostics in their clinical development programmes for patient selection or stratification, working as a strategic and integrated expert partner, taking full sponsor ownership of the IVD study being conducted in parallel with our clients' IND/IMP trial. ARC's team of experts cover IVD regulatory compliance, study design and approvals, quality assurance including vendor due diligence and management along with a team of clinical research experts who manage the IVD study, ensuring it is conducted in compliance with local and global GCP, and that the biomarker data is robust and reliable. To further support our growing client base and to expedite patient access to life-saving experimental medicines, ARC has developed and launched our SaaS platform, ARC360. ARC360 is transforming how organisations access regulatory intelligence and tailor study-specific information for using in vitro diagnostics to select and manage patients in IND trials. Powered by cutting-edge technologies and supported by a team of regulatory, quality, and clinical operations experts, ARC360 is designed to accelerate the initiation of complex clinical trials. Job Description To be an integral member and significant contributor to project team(s) in the development and delivery of global compliance solutions to client companies, ensuring that client objectives are met and exceeded at all times. This will require the utilisation of a platinum standard approach to regulatory research, internal and external stakeholder satisfaction as well as an innate work ethic and attention to detail that is aligned with the company’s core values. • Support the work of the company and project teams in the provision of specialised regulatory and quality assurance expertise to client companies, ensuring client expectations and interests are met., • Research and prepare elements of regulatory submission documents on behalf of client companies, including but not limited to study risk determination requests, IDE submissions, 510(k), PMA, CE Technical Files and Design Dossiers, PMDA Briefing Documents and Submissions etc., • Assist wider team in understanding the regulatory requirements for an investigational device in the set-up, management & conduct of IVD performance studies worldwide., • Manage and keep up to date information relating to regulatory requirements for IVD performance studies and maintain the company’s web-based clinical trial planning tool., • Conduct gap analyses on behalf of client companies and prepare associated reports, • Contribute to the preparation of global guidance documents and white papers., • Contribute to the preparation of other regulatory documents on behalf of client companies (e.g., Performance Evaluation Plans/Reports, Investigator Brochures, etc)., • As required, take advantage of professional networking opportunities to promote the company and its services to appropriate parties., • Undertake continuing professional development activity to ensure awareness of current quality and regulatory standards., • Contribute to ARC company culture initiatives to maintain a positive and engaging workforce., • Any other duties, within reason and capability, as determined by company management. Essential Criteria • Engineering or Scientific honours degree or equivalent (10+ years) relevant industry experience, • 5+ years’ experience of working in a medical device/IVD manufacturing or regulatory environment, • Experience with IVD/CDx design and development, from feasibility to approval, • Knowledge of regulations in key global markets as they pertain to IVD and/or CDx devices (e.g. EU/US), • Experience of leading global regulatory submissions (e.g. EU/FDA), • Experience developing and maintaining technical documentation (IVDD/IVDR) or design history file documentation (FDA), • Experience developing global regulatory strategies for IVD devices “We are an equal opportunity employer; applications are welcome from all and appointment will be made on the basis of merit.”

ARC's purpose is to expedite access to precision medicine clinical trials for patients globally. We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and the important relationships we have developed with our global clients. We are a Belfast-based Clinical Research Organisation that specialises in delivering compliance excellence for companies in the precision medicine sector. We support many of the world's leading pharmaceutical R&D companies in implementing unapproved diagnostics in their clinical development programmes for patient selection or stratification, working as a strategic and integrated expert partner, taking full sponsor ownership of the IVD study being conducted in parallel with our clients' IND/IMP trial. ARC's team of experts cover IVD regulatory compliance, study design and approvals, quality assurance including vendor due diligence and management along with a team of clinical research experts who manage the IVD study, ensuring it is conducted in compliance with local and global GCP, and that the biomarker data is robust and reliable. Job Purpose: To be an integral member and Clinical Lead to project team(s) in the development and delivery of ARC’s Sponsor Delegation offering to client companies, ensuring that client objectives are met and always exceeded. This will require the utilisation of a platinum standard approach to clinical research project management, internal and external stakeholder satisfaction as well as an innate work ethic that is aligned with the company’s core values. Key Responsibilities: • Study design, strategy, planning (timeline, resources and budget management)., • Coordinating clinical operational activities with internal stakeholders and clients, including pharma company and central testing laboratories conducting the studies., • Development and /or review of associated documentation including documents such as CPSP, CSP, investigator brochure, informed consent for devices, risk-based monitoring plan and reports, in compliance with relevant regulations, guidelines and SOPs., • Client management, issue resolution, troubleshooting and ongoing coordination between all relevant groups to maintain compliance to protocol, patient safety and robust data collection and provision of regular updates to project progression., • Set up, manage and track studies, supporting study completion within agreed timelines and budget. Identify and enlist suitable study sites, and coordinate site management activities, with site audit, Site Qualification Visit, and study set up across USA, EU and Asia/Pac regions., • Understanding and application of relevant regulatory requirements and ethical approvals for conducting studies (e.g. IVDR requirements for EU, FDA requirements for USA, GCP, ISO20915)., • Managing the study close out activities including, essential documentation filing and completion between study testing site(s) and sponsor TMF, ethical and regulatory bodies notification of study close, study close out report., • Generation of clinical study reports and related documentation to submit to regulatory authorities, ethical review boards and local agencies such as national competent authority. Essential Criteria: • Undergraduate degree in biological sciences or other related scientific subject., • Minimum 3+ years clinical experience in an IVD device manufacturer; other devices or pharmaceutical experience in the capacity of device sponsor will be considered., • Demonstrable knowledge of regulatory requirements and industry practices (e.g. IVDR, FDA, GCP, ISO14155, ISO20916, ISO13485, and QMS design control)., • Experience of using TMF and/or eTMF and Smartsheet (or equivalent) software., • Experience of authoring clinical study documents (e.g. Clinical Strategy, Data Management Plan, CPSP, CSP, Investigator Brochure, Risk-based Monitoring Plan, Informed Consent Documents)., • Proof of Right-to-Work in the UK. “We are an equal opportunity employer; applications are welcome from all and appointment will be made on the basis of merit.”

ARC's purpose is to expedite access to precision medicine clinical trials for patients globally. We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and the important relationships we have developed with our global clients. We are a Belfast-based Clinical Research Organisation that specialises in delivering compliance excellence for companies in the precision medicine sector. We support many of the world's leading pharmaceutical R&D companies in implementing unapproved diagnostics in their clinical development programmes for patient selection or stratification, working as a strategic and integrated expert partner, taking full sponsor ownership of the IVD study being conducted in parallel with our clients' IND/IMP trial. ARC's team of experts cover IVD regulatory compliance, study design and approvals, quality assurance including vendor due diligence and management along with a team of clinical research experts who manage the IVD study, ensuring it is conducted in compliance with local and global GCP, and that the biomarker data is robust and reliable. To further support our growing client base and to expedite patient access to life-saving experimental medicines, ARC has developed and launched our SaaS platform, ARC360. ARC360 is transforming how organisations access regulatory intelligence and tailor study-specific information for using in vitro diagnostics to select and manage patients in IND trials. Powered by cutting-edge technologies and supported by a team of regulatory, quality, and clinical operations experts, ARC360 is designed to accelerate the initiation of complex clinical trials. Job Purpose To be an integral member and significant contributor to project team(s) in the development and delivery of global clinical compliance solutions to client companies, ensuring that client objectives are met and exceeded at all times. This will require the utilisation of a platinum standard approach to clinical research, internal and external stakeholder satisfaction as well as an innate work ethic that is aligned with the company’s core values. Key Responsibilities: • Research and prepare clinical elements of regulatory submission documents on behalf of client companies, including but not limited to CPSP’s, IB’s & Annex XIV submissions, Study risk determination requests, IDE submissions, IRB/REC Submissions., • Assist wider team in understanding the clinical operations requirements for an investigational IVD in the set-up, management & conduct of IVD clinical investigations worldwide., • Prepare clinical affairs/operations quality management system audit reports and gap analyses on behalf of client companies., • Contribute to the preparation and/or delivery of global clinical research guidance documents, conference presentations, webinars, white papers and other company-developed materials as required., • Ongoing project budget management and tracking. Essential Criteria: • Undergraduate degree in biological sciences or other related scientific subject., • Minimum 3+ years IVD medical device clinical affairs/R&D experience in a similar role or 3-year post-doc experience in a relevant research subject., • Demonstrable awareness of the requirements of clinical performance studies in accordance with the EU IVDR, as well as relevant regulations (eg: ISO 20916, 21 CFR)., • Demonstrable awareness of IRB/IEC (ethics) submission requirements., • Experience of generating and reviewing documents relevant to clinical studies (eg: Strategy, Clinical Protocol, Monitoring Plans, Monitoring Reports)., • Proof of Right-to-Work in the UK., • Must be able to commute daily to Belfast as job is on-site. Desirable Criteria: • Postgraduate degree in biological sciences or other related scientific subject, • Prior experience working in a rapid growth, SME environment., • Experience of clinical research regulatory requirements for companion diagnostics in the US., • Strategic planning for IVD clinical studies, including identification and qualification of suitable clinical investigation sites., • Experience of risk management and CAPA systems., • Experience of eDC and eTMF platforms., • Experience of working with NHS R&D. “We are an equal opportunity employer; applications are welcome from all and appointment will be made on the basis of merit.”

BHSCT Assistant Services Manager (ASM) /Lead Nurse, Medicine and Medical Specialties Band 8A. The post holder will assist the Service Manager in the development, co-ordination and delivery of high-quality service within RBHSC. The post holder will be the conduit between Service Manager and the front

A healthcare recruitment agency in the UK is seeking an Assistant Services Manager to assist in the development and delivery of high-quality healthcare services.This role involves leading clinical teams, ensuring efficient resource use, and maintaining strong communication among multidisciplinary te

A leading healthcare recruitment agency in the United Kingdom seeks Registrar / Speciality doctors for Emergency Medicine.

The Royal Victoria Hospital require a Registrar (Middle Grade) to work in their Neurology Department.

Hospital: Royal Victoria Hospital.

ARC Regulatory is a Belfast-based Clinical Research Organisation specialising in compliance excellence for precision medicine. ARC360 is our SaaS platform transforming how organisations access regulatory intelligence and tailor study‑specific information for in‑vitro diagnostics to select and ma

Specialist Hospitals and Women's Health. To view the full job description and apply for this position please click the Job Details and apply button below. Our help section provides guides and support information to candidates completing the application form.

Research Impact and Engagement Officer (Medical, Health and Life Sciences). You will work in close partnership with academic and professional colleagues across the Faculty of Medicine, Health and Life Sciences (MHLS) to support and enhance research engagement and impact.

ARC’s purpose is to expedite access to precision medicine clinical trials for patients globally.We fulfil our purpose through our dedicated team of experts with unparalleled domain knowledge, and the important relationships we have developed with our global clients.We are a Belfast-based Clinical

A healthcare provider in Belfast is looking for a part-time Registered Nurse (RN) to lead care teams and deliver high standards of care. Responsibilities include overseeing medicine management, developing care plans, and ensuring compliance with regulations.

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Precision for Medicine is hiring an experienced Change Orders Manager based in the UK to join our global

Experience in occupational health, medical assessments, or fitness-for-work determinations. Preferred: Membership of the Faculty of Occupational Medicine (MFOM). Alternative: MRCGP with a Diploma in Occupational Medicine.

Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Precision Medicine Group is an Equal Opportunity Employer. Precision for Medicine is hiring an experienc

Clinical Lead/ Charge Nurse £21.90p/h Great Pension Excellent holidays Exceptional career development Newtownabbey area RightFit are excited to be recruiting for a dedicated Charge Nurse/ Clinical Lead to come join one of Newtownabbeys well respected care homes. This is an excellent opportunity with a great salary and benefits package. What’s on offer? · £21.90p/h · Exceptional career progression · Ongoing training and development · Excellent pension · Great holiday entitlement · Supportive team · Free parking What you will do as a Charge Nurse/ Clinical Lead · Leading a team of care staff to deliver exceptional care · Producing well-developed care plans and detailed risk assessments, with an understanding of regulatory frameworks · Maintain accurate documentation and resident records whilst incorporating the use of modern technology · Overseeing all aspects of medicine management on your shift in accordance with company policies and current legislation What you will need as a Charge nurse/ Clinical Lead: · Qualified RGN, RMN or RNLD · Experience in a similar role · Active NMC Pin If this sounds like the role for you apply today

Specialist Advisor – General Internal Medicine Consultant Doctor - Homebased - Region specific, United KingdomJob title: SpecialistAdvisor – General Internal Medicine Consultant Doctor Location: National Daily rate: £300 (£268 day rate + £32 day holiday pay) Ad-Hoc: As and when requir

Permanent | Full-Time or Part-Time.Compass Associates are partnering with a leading UK-based, digital-first healthcare provider operating within a rapidly expanding specialist prescribing space.Manage chronic musculoskeletal, neuropathic and complex pain presentations.Operate within a structured pre

At least five years in Emergency medicine posts.

Precision Medicine Group is an Equal Opportunity Employer.

Precision Medicine Group is an Equal Opportunity Employer.

Lead and manage the Sport Science & Medicine department within the Academy. Be responsible for the management and delivery of the Sport Science and Medicine/Performance Support Programme for all Academy Players registered with the club. Ensure the Academy Sport Science & Medicine department are comp

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Small Animal Internal Medicine. Applications are invited from veterinary graduates for the above residency specialties as part of the Professional Doctorate in Veterinary Medicine full-time, postgraduate programme of studies. The successful candidates will be enrolled with the University of Edinburg

A leading digital health provider in the United Kingdom seeks a GMC-registered Consultant in Pain Management for a remote role.You'll assess and manage patients considering cannabis-based treatments for psychiatric conditions, with emphasis on clinical decision-making.The position offers flexible wo

A leading medical recruitment agency in the UK seeks individuals aiming to become A&E doctors.The role involves diagnosing and treating emergency patients, working in various settings, and participating in ongoing training.Candidates must have a medical degree and complete specific training programs

Here at Triple West Medical, we are currently recruiting on behalf of an NHS Trust in Northern Ireland and they have requested our assistance to help recruit a Locum FY1 in Surgery/Medicine for a 3 month contract at the trust.

A leading pharmaceutical firm is seeking a Product Analyst to expand their portfolio across the UK, Ireland, and Malta.The ideal candidate will have a Master's Degree and up to two years of experience in product analysis.Responsibilities include market research, product performance evaluations, and

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This role is for one of our clients.In this non-clinical role, you will apply your clinical expertise to evaluate AI-generated medical content, ensuring accuracy, patient safety, and adherence to current standards of care.Instead, you will play a key role in shaping the future of AI applications in

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This year, we’re proud to celebrate our 25th anniversary, marking a quarter-century of placing healthcare professionals in locum roles across both the public and private sectors in the UK and Ireland.Our long-standing reputation speaks to the trust and reliability we’ve built within the healthca

A leading veterinary service provider in the United Kingdom is seeking passionate Internal Medicine clinicians to join their developing service. This role involves overseeing referral-level medicine cases and maintaining client communications.

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A health regulatory body in the UK is seeking a Specialist Advisor to contribute to the regulation of healthcare services.This role focuses on assessing the quality of medical services and providing expert advice that influences regulatory processes.Applicants must be GMC registered specialists with