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Fertility Doctor – New Private Clinic | Belfast Contract: Part-time or Full-time | Competitive Salary + Benefits An established private healthcare group is launching a state-of-the-art fertility clinic in Belfast, and we’re seeking an experienced Fertility Doctor to join the founding clinical team. The Opportunity This is a rare opportunity to play a key role in building a new fertility service from the ground up. You’ll be part of a supportive, nurse-led model that allows doctors to focus on what matters most — delivering outstanding patient care through consultations and procedures. With exceptional facilities, a collaborative clinical environment, and activity levels above the national average, this role offers both professional fulfilment and genuine career progression. About You • GMC registration, • Experience in reproductive medicine and/or IVF, • Compassionate, patient-focused approach and strong communication skills, • Commitment to a structured working pattern (part-time options available) What’s on Offer • Competitive base salary, generous relocation package plus performance-related bonus, • Supportive clinical leadership and governance within a trusted private healthcare group, • The chance to influence the development and success of a new fertility service in Northern Ireland, • Modern working environment and dedicated administrative support If you’re passionate about helping people achieve their dream of parenthood and want to make your mark in a new, forward-thinking clinic, we’d love to hear from you. 📝 Ready to take the next step in your medical career? Hit Apply now or Email Camila at 📞 Call 02392 384 900 for a confidential chat.

Medical Director – New Fertility Clinic Contract: Full-time Competitive Salary + Relocation Package + Bonus + Benefits An established private healthcare group is opening a brand-new, state-of-the-art fertility clinic in Belfast, and we’re seeking an experienced Medical Director to lead the service from its inception. The Opportunity This is a career-defining leadership role for a forward-thinking fertility specialist who wants to shape the direction of a brand-new clinic from day one. As Medical Director, you’ll have full clinical oversight — helping to design protocols, lead recruitment, develop service pathways, and build a high-performing, patient-centred team. You’ll work within a collaborative, nurse-led model that allows doctors to focus on clinical excellence while maintaining robust governance and operational efficiency. With cutting-edge facilities and the backing of a respected healthcare group, this is a chance to make a lasting impact on fertility care in Northern Ireland. About You • GMC registration with a background in Reproductive Medicine / IVF, • Proven experience in clinical leadership or service development, • Passionate about innovation, patient safety, and evidence-based practice, • Strong communication and mentorship skills, • Commitment to continuous improvement and multidisciplinary collaboration What’s on Offer • Highly competitive base salary with performance-related bonus and relocation package, • Opportunity to build and lead a new fertility service with full autonomy and senior clinical influence, • Supportive executive team and established governance framework, • State-of-the-art working environment and administrative support, • Long-term potential for growth within a well-funded private healthcare group If you’re ready to lead a pioneering fertility clinic and shape the future of reproductive medicine in Belfast, we’d love to hear from you. 🩺 Interested in finding out more? 📧 Email Camila at 📞 Call 02392 384 900 for a confidential discussion.

Are you passionate about psychological services that support the rehabilitation of service users? We're recruiting on behalf of Belfast Health and Social Care Trust to add an Assistant Psychologist within their Adult Psychological Therapies Service. As a member of the team, you assist in clinically related administration, conduct of audits, collection of statistics, and development of audit and/or research projects, teaching and project work as relevant to the post. The post holder will be exposed to aggressive/highly distressed behaviour from patients and family members. Training in the management of aggression is mandatory and staff will be provided with access to panic alarms. The role: • Conduct psychological assessments using tests, interviews, and observations to inform care plans., • Support the delivery of psychological treatments and therapeutic group sessions under supervision., • Maintain detailed, accurate clinical records and manage data entry across Trust systems., • Contribute to research, audits, and service evaluations, analysing data and preparing reports., • Uphold Health & Safety standards during clinical work, including safe manual handling and professional conduct in challenging situations., • Participate in supervision, training, and ongoing professional development to enhance service delivery., • Collaborate effectively within multidisciplinary teams, supporting consistent, high-quality patient care. The Person As the successful candidate you will have the following background and experience: Essential: • Psychology graduate- minimum of 2nd class hons or higher., • Previous experience as a assistant psychologist. Entitlement to graduate membership of the British Psychological Society. * Experience of conducting neuropsychological/ psychometric assessments (e.g. WAIS-IV) under supervision. What's in it for you?: • Salary: £29,970 per annum., • Generous annual leave allowance., • Excellent progression opportunity. To speak in absolute confidence about this opportunity please send an up to date CV via the link provided or contact Zachery Downes Specialist Consultant at MCS Group 02896935501. Even if this position is not right for you, we may have others that are. Please visit MCS Group to view a wide selection of our current jobs MCS Group is committed to Equality, Diversity, and Inclusion for all, being the first recruitment agency in NI to achieve Bronze Diversity Mark accreditation, if you have a disability which means you require a reasonable adjustment to be considered at any stage of the recruitment process, please contact us and we will endeavour to facilitate the request. "This position is subject to an Enhanced (Basic/Standard) criminal record check through AccessNI. A criminal record will not necessarily be a bar to obtaining the position". Not all agencies are the same…MCS Group are passionate about providing a first-class service to all our customers and have an independent review rating of 4.9 stars on Google.

Are you a recent science graduate looking to start a rewarding career in healthcare? MCS Group is proud to partner with the Health and Social Care Trusts across Northern Ireland (HSCNI) to recruit Laboratory Technicians for a range of opportunities within hospital laboratories. This is an excellent opportunity to gain hands-on experience in a professional laboratory setting, supporting essential diagnostic and clinical services that make a real difference to patient care. The Role As a Laboratory Technician, you will: * Prepare, process, and analyse patient samples in line with standard operating procedures. * Perform routine laboratory tests and assist with specialist investigations under supervision. * Maintain equipment and ensure quality control standards are met. * Support Biomedical Scientists and senior staff with service improvement and audits. Essential Criteria * Degree in a science-related subject (Biomedical Science, Biology, Chemistry, or similar). * Strong attention to detail and accuracy. * Good teamwork and communication skills. * Enthusiasm to learn and develop within a healthcare laboratory environment. What's in it for you * Salary: £23,000-£26,000 per annum (Band 3-4, depending on experience). * Generous annual leave allowance. * Comprehensive training and mentoring from experienced professionals. * Clear career progression opportunities within HSCNI laboratories. This is an exciting chance for science graduates to gain valuable laboratory experience and begin a meaningful career with one of Northern Ireland's largest public sector employers. To discuss Laboratory Technician opportunities across the HSCNI in confidence, please send your CV via the link provided or contact Zachery Downes, Specialist Consultant at MCS Group, on 028 9693 5501. Even if this opportunity isn't right for you, MCS Group may have others that match your skills and career goals. Visit to view all current roles. MCS Group is committed to Equality, Diversity, and Inclusion, and is proud to be the first recruitment agency in Northern Ireland to achieve Bronze Diversity Mark accreditation. If you require a reasonable adjustment at any stage of the recruitment process, please contact us. This position is subject to an Enhanced (or Basic/Standard) AccessNI check. A criminal record will not necessarily be a bar to obtaining employment.

Approved WCA Functional Assessors – Remote Role Salary: • £42,000 per annum (newly approved) What We Offer: • Competitive salary with experience-based uplift, • Fully remote working – achieve true work-life balance, • Ongoing professional development and support As a WCA Functional Assessor, you’ll use your clinical expertise to assess individuals and provide detailed, evidence-based reports that help inform important decisions. You’ll work autonomously, supported by a dedicated team, and play a vital role in improving lives. Requirements: • NMC/HCPC/GMC registration (or equivalent), • Excellent communication and report-writing skills, • Strong clinical judgement and attention to detail Apply now and join a team that values your skills and supports your growth.

Insurance Solicitor Belfast I'm currently partnering with one of Northern Irelands most respected commercial law firms, which is seeking to expand its Defence Litigation team.This is a fantastic opportunity for a qualified solicitor with strong experience in defendant personal injury or clinical neg

We are seeking to appoint a registrant member for our governing Council. Our Council comprises 12 members from across the UK (six lay and six registrant). We are currently seeking a new registrant member who will be able to bring their strong frontline clinical experience and demonstrable board leve

We are working with a top-tier national law firm based in Belfast who are seeking solicitors at all levels to join their Clinical Negligence team. The Role: The successful candidate will join a highly regarded Clinical Negligence team, providing legal services to a broad spectrum of healthcare professionals, with a focus on defence litigation. The candidate’s duties will include defending high-value clinical negligence claims and supporting clients through managing risk, complaint handling, serious incident investigations throughout the litigation process. Throughout the role, the candidate will gain an in-depth understanding of the complexities and challenges of all areas of clinical practice frequently faced by practitioners and organisations. The candidate will also demonstrate a willingness to contribute to business development while managing client relationships. Essential Criteria • NQ+;, • Strong background in medical negligence and/or dispute resolution;, • Outstanding academics;, • Technically excellent;, • Negotiation skills;, • Willingness to become involved in business development;, • Ability to work independently and as a team. Benefits • Excellent salary package (commensurate with experience);, • Generous benefits package;, • Extensive opportunities for career development;, • Excellent client base;, • Hybrid working;, • Inclusive and friendly culture. Please contact Andrew Currie on +44 7519 489 330 or email if you would like to have a confidential discussion about this opportunity.

Role: Patient Care Advisor Hours: Full time, 40 hours per week Location: Belfast, fully on-site Salary: £26,000 plus bonus Optical Express is focused on delivering exceptional patient care, outstanding clinical outcomes and continued investment in our people and technology. For over 34 years, millions of patients have trusted Optical Express with their eye care. As Europe’s leading private provider of laser eye, premium intraocular lens and cataract surgery, our Surgeons undertake more laser procedures collectively than any other provider. We look after thousands of patients in our clinics every week and it’s a privilege to transform the lives of so many. The Optical Express team work together, collectively and consistently striving for excellence. We support each other, respect each other and are committed to a culture of care, trust and integrity. The culture extends to our local communities, through our range of charitable and environmental projects. We focus on doing what is right for our patients, our colleagues, our local communities and our planet. Do you want to be part of a team that literally changes lives? In return you’ll have the opportunity to develop your career through ongoing training and development. Each day will vary however the core components of your role will include: • Engaging with existing customers/patients, • Handling customer enquiries quickly and efficiently, • Understand customers/patient demand and needs, • Overcome objectives and resolve them, • Maintain and develop product knowledge and customer service skills, • Accurate maintenance of patient records Essential skills • Excellent verbal and written communication skills, • The ability to deal with customers over the telephone in a confident and professional manner, • A willingness to learn, • Sales experience, • Excellent rapport building and communication skills with the ability to overcome objections What’s in it for you? • Rewarding salary, • Bonus incentives, • Free or discounted optical products/procedures, • Discounted prescription and non-prescription eye care (including family), • Career progression, • Cycle to work scheme This is a fantastic opportunity to join an established organisation where you will have the support to grow and develop within a professional working environment. If you are interested in being considered for the role please apply now. Optical Express is an equal opportunities employer

About Us Sonrai is a Belfast-based AI precision medicine company that helps Biotech and Pharma companies get maximum value from their data, with a mission to power the most important precision medicine breakthroughs through connected data and collaborative science. We enable our customers to reduce the cost, time, and risk from early discovery to clinical trials, accelerate drug, biomarker, and diagnostics development, maintain a secure and compliant Trusted Research Environment, and effectively and safely manage data. Our bioinformatic cloud product, Sonrai Discovery, is sold on a license fee basis, along with accompanying data science and software engineering professional services. Our clients and partners already include some of the biggest names around, and we’re now looking to appoint a Senior Quality and Regulatory Engineer to help deliver our strategy. It’s a great time to be joining Sonrai; over the past two years, we have: • Successfully grown our customer base across a range of biotech and pharma organizations globally, • Grown our team to 35+ and won multiple awards Opportunity & Responsibilities The Senior Quality and Regulatory Engineer role is a permanent role, with onsite office work in Belfast at least 2 days a week and home-working. The role will report into the Quality and Regulatory Manager (and Head of Operations during maternity leave period, with ongoing direction from an external Quality and Regulatory consultant). Sonrai are looking to fill this role as soon as possible. The Senior Quality and Regulatory Engineer will be responsible for ● leading on quality projects to implement applicable requirements of ISO 27001, with a nominated set of subject matter experts across the business, ● managing and maintaining processes for EU and UK GDPR, and UK Data Protection Act, identifying and implementing new data protection requirements for new markets, and supporting the Data Protection Officer in customer requests, ● managing and maintaining Sonrai’s Quality Management System and certification, with support from the consultant, including performing internal audits, ● maintaining quality system and product compliance by identifying new and changes regulatory obligations that affect Sonrai’s business and customers, this includes performing gap assessments and building compliance and implementation plans with the support of subject matter experts across the business, ● supervision of 1 Officer level staff member. Essential Criteria The person: ● A detail-orientated, proven multi-tasker who can adapt to the needs of a small dynamic business ● Team player with strong collaborative abilities and communication skills ● Self-motivated with a growth mindset ● Right to work in the UK or Ireland for a minimum of 2 years from the date of any job offer from Sonrai ● Proficient to a relevant level of Business English The experience: ● Software development quality experience, can be with medical devices, drug development or another regulated environment ● Proven, direct ISO 27001 working experience and knowledge ● Data Protection legislation experience, minimum EU and UK GDPR ● Proven internal auditing experience Desirable Criteria (what you will learn at Sonrai!) ● Experience working in a certified ISO Quality Management System, such as ISO 9001, ISO 13485 certified QMS with EN 62304, ISO 14971 product development standards ● US data protection legislation experience ● Knowledge/awareness of the AI Act and vulnerability management processes ● Awareness of AWS as cloud infrastructure ● EU IVDR 2017/746 or EU MDR 2017/745 and UK Medical Device Regulation experience ● Lead Auditor certification Sonrai Employee Benefits ● Competitive salary ● Employer pension contribution ● Hybrid working ● Flexible working available including Flexi Fridays and No Meeting Fridays ● 25 days leave plus 10 public/bank holidays ● Membership of Westfield Health Plan ● Enhanced Maternity Leave (including 16 weeks at full pay) and Paternity Leave (2 weeks at full pay), once probationary period is successful ● Training budget / strong focus on staff development ● Equipment / working from home budget (up to £300 for home office furniture) ● Membership of Women in Business Northern Ireland More than a Job We’re working with global research leaders and industry powerhouses to enable and support truly life-changing advancements within healthcare analytics, bioinformatics, and precision medicine. We’re driven by the potential impact our products might have on supporting ground-breaking predictions and we’re seeking passionate individuals to help us accelerate those plans. To apply, please send a CV and covering letter outlining how you meet the above criteria, together with a completed Equal Opportunities Monitoring Form, to Alice Geaney at For data protection reasons Sonrai retains CVs and other pertinent information of applicants for 12 months after application, following this, records are deleted. Sonrai does not retain CVs on file for future roles. By submitting your application, you consent to the processing of your personal data for the purposes of recruitment and in accordance with applicable data protection laws and regulations. Please refer to our Privacy Policy on our website for further details. Don’t meet every single requirement? Research indicates that women and underrepresented individuals often hesitate to apply for roles unless they meet all qualifications. At Sonrai, we're committed to fostering a diverse, inclusive, and authentic work environment where employees know they are valued, respected and heard. If you're enthusiastic about the position but don't match every qualification, we urge you to apply. You could be an ideal fit for this or other roles. If you have a disability and require adjustments through the recruitment process, please let the contact on the Job Description know, Sonrai will endeavour to make reasonable adjustments.

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 ARCs laboratory team in the design, implementation and execution of internal and client laboratory IVD or CDX studies, ensuring that client objectives are met and exceeded at all times. This will require the utilization of regulated experimental approaches to clinical studies, internal and external stakeholder satisfaction as well as an innate work ethic that aligns with the company’s core values. Key Responsibilities: The R&D Scientist is expected to: • Develop, optimise and validate assay protocols for molecular assays including PCR and Next generation Sequencing, • Conduct experiments to troubleshoot and refine processes to improve assay sensitivity, specificity, and reproducibility., • Conduct analysis of biomarker levels in biological samples., • Analyse and interpret experimental data, preparing comprehensive reports and presentations for stakeholders., • Stay updated with the latest advancements in relevant scientific techniques to inform laboratory activities., • Maintain accurate laboratory records and ensure compliance with safety and quality standards Essential Skills & Experience • Bachelors degree in biological sciences or other related scientific subjects, • Minimum 3+ years’ experience in designing and implementing, PCR/NGS and or ELISA experiments, • Strong understanding of assay verification and validation in line with regulatory standards such as IVDR and CLSI, • Experience working within a regulated laboratory environment (ISO17025/ ISO15189 / CAPCLIA), • Excellent interpersonal skills and presentation skills, • Excellent problem-solving skills and the ability to work independently as well as part of a team, • Able to work flexibly as required to ensure business needs are met., • Proof of Right-to-Work in the UK., • Must be able to commute daily to Belfast as job is 100% on-site. Desirable Skills & Experience • MSC/PhD in biological sciences or other related scientific subjects, • Previous experience in a commercial laboratory, • Experience in IHC/histology, • Prior experience working in a rapid growth, SME environment, • Experience with IVDR/IDE regulation, • HEP B Vaccinated (willingness to be vaccinated at start of role) “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 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 companys 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 companys 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. Skills: Regulatory Affairs IVDR CDx

Description At System C, we create software that helps drive 21st century health and social care in the UK. Using leading-edge technology and data, our systems are trusted by hundreds of health and social care organisations, our work impacts millions of lives every day. What we do matters. We are looking for a clinically experienced Pre-sales specialist who delivers high-impact demonstrations and proposal support to NHS customers. This role blends clinical insight with software fluency to help shape compelling solution stories that align with NHS strategy, workflows, and policy drivers. Key Responsibilities: Lead and deliver tailored product demonstrations to clinicians and NHS stakeholders Translate complex NHS requirements into impactful software narratives Co-create bids, tender responses, and value propositions with the Sales team Support ROI cases and client-specific solution design Prepare demo data, test environments, and customer-specific workflows Build internal capability by sharing NHS workflow knowledge with technical and product teams Contributes to solution shaping across acute, community or cross ICS bids Manages multiple bid opportunities in parallel Write and support high-quality bid responses, including ROI narratives Represent System C at events, exhibitions and client workshops Required Skills: Strong clinical background (Pharmacy) Confident presenter with ability to engage both clinical and executive audiences Knowledge of NHS policy landscape and EPR convergence objectives Skilled in demonstration delivery, objection handling, and bid support Skilled in stakeholder management and proposal development Organised, detail-focused, and able to manage pre-sales cycles and deadlines at pace Experience: Experience delivering software demonstrations in clinical environments Supporting formal bids (PMEs, ITTs, Outline Business Cases) Liaising with Sales, Product, and R&D to close clinical and functional gaps Responding to technical questions with credible, patient-centred use cases

Litigation Solicitor, East Belfast, NQ-5 YRS PQE. Overview A well-established and growing law firm based in East Belfast, specialising in personal injury, credithire, accidents at work, clinical negligence, and other litigation matters, is seeking a Solicitor (NQ 5 years PQE) to join their busy and dynamic team. This is an excellent opportunity for a solicitor looking to develop their litigation career across a broad range of contentious work while receiving strong support and mentoring. Key Responsibilities Manage a caseload of Motor Claims. Draft legal documents, correspondence, and court bundles, ensuring compliance with deadlines and procedural requirements. Attend client meetings, medical appointments, and court hearings as required. Liaise with clients, insurers, counsel, and other stakeholders to progress cases efficiently. Assist senior solicitors with case strategy and file management. Maintain accurate case records and ensure all administrative and compliance requirements are met. Essential Skills and Experience Qualified solicitor with NQ to 5 years PQE Strong advocacy, negotiation, and drafting skills. Ability to manage multiple files and deadlines independently. Excellent communication skills, both written and verbal. Proactive, organised, and able to work collaboratively in a team environment. Experience attending court hearings is advantageous. Whats on Offer Opportunity to work in a well-respected and supportive litigation team. Exposure to a diverse caseload across PI, credit hire, accidents at work, clinical negligence, and other litigation matters. Competitive salary and benefits package. Flexible working excellent holidays Structured mentoring and career development opportunities for solicitors looking to progress their litigation experience. If you would like a confidential discussion about the role, please contact Orla Milligan at Pathway. At Pathway, we treat all applications with the highest level of confidentiality and professionalism. In line with GDPR regulations, your personal information will only be used for recruitment purposes, stored securely and never shared without your consent. You can request to have your data removed at any time. Skills: personal injury litigation clinical negligence credit hire Benefits: excellent holidays flexible working career development

Clinical Negligence (Defence) Solicitor, Belfast The Opportunity: A law firm in Belfast is keen to attract applications from enthusiastic solicitors wishing to join their growing healthcare team. You will join a competitive team and handle a varied caseload of defendant clinical negligence claims, including matters involving doctors, nurses, private hospitals, and other healthcare providers. Youll advise clients on complex medical, legal, and procedural issues, working closely with both insurers and insured professionals to achieve successful outcomes. Your work will include: Managing a diverse caseload of clinical negligence and healthcare-related claims from instruction through to resolution. Advising insurers and their insureds (including hospitals, consultants, and medical practitioners) on liability, quantum, and strategy. Drafting pleadings, witness statements, and instructions to experts and counsel. Liaising with clients, experts, and barristers, ensuring cases progress efficiently and proactively. Assisting senior partners on high-value and complex group actions. Staying up to date with developments in healthcare law, case law, and industry practice. The Person: Ideally, you will offer some experience of handling a range of clinical negligence claims, perhaps working for a large law firm or a boutique legal firm operating. The PQE range is flexible as is the title e.g. Associate, Snr Associate. Alternatively, if you are operating in a different area of law and can offer transferable skills and a strong positive learning attitude, then the team will commit to supporting your development. Indicatively this may reflect solicitors currently providing defence expertise in EL/PL or car insurance. Also, if you are operating in healthcare / litigation and wish to shift from plaintiff to defence, then lets explore. Rewards: You will gain a highly attractive base salary, bonus scheme and excellent benefits. In addition to the financial reward, this client offers ongoing training and support as well as a career progression plan. You will also gain an opportunity to work with top-tier insurance and healthcare clients, operate in a supportive, collaborative team environment with real career progression. And benefit from hybrid working options and flexible arrangements. Ifthis role sounds right for you, then send an updated CV through the link or contact Alan Braithwaite for an honest and confidential discussion. VisitAbacusCareers for other opportunities and view the 2025 Salary Guide.Abacus has been hiring the best legal talent for 20 years, from Partner to Paralegal across Practice & In-House. We have helped shape the careers of 1000s of legal and finance professionals since 2003 and helped 100s relocate back to Northern Ireland. Skills: solicitor healthcare clinical

Assist wider team in understanding the regulatory requirements for an investigational device in the set-up, management & conduct of IVD performance studies/clinical investigations worldwide (e. IVD manufacturing or regulatory environment. Experience of leading global regulatory submissions (e.

Physiotherapist / Physio / Clinical Support / Surgical Sales / Clinical Sales / Scrub Nurse / Female Healthcare Specialist / Gynaecology / Urology / Belfast / Ireland North. Years’ experience as a hospital-based Physiotherapist (NHS or Private). Physiotherapist / Physio / Clinical Support / Surgic

Our client requires an experienced Pharmacist with Oncology experience to start as soon as possible. NHS Hospital experience essential. Experienced and dedicated compliance consultants.

Position: Senior Clinical Research Associate (12+ months’ monitoring experience required). Up to 2 years of pharmaceutical industry experience or other relevant experience (NHS or Academic). Senior Clinical Research Associate (CRA) with a focus on monitoring clinical trials for a global pharmaceut

Checks the site and external facilities, equipment, and supplies (clinical and non-clinical) continue to be adequate to conduct the trial and with their expiry dates (as applicable). Recent oncology experience will be essential. Per the Clinical Monitoring Plan (CMP) or SMP: Ability to conduct monit

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

Belfast Customer Service Centre .OTE of £33000 with quarterly bonus and potential overtime.Shift Pattern: 5 over 7 (Tuesday - Saturday).At Currys we’re united by one passion: to help everyone enjoy amazing technology.As the UK’s best-known retailer of tech, we’re proud of the service our cus

No experience needed – just bring your motivation.

We are seeking an experienced, motivated, and inclusive professional who can lead by example and deliver high-quality arboriculture services. Proven experience in arboriculture, including pruning, felling, planting, and maintaining tree health and safety. Experience delivering customer-focused servi

No experience needed – just bring your motivation.

Thats why we prioritize integrating diversity, equity, inclusion and belonging principles into the core of how we work every dayfocusing not only on our employee experience, but also our customer experience and operations. In this role, you will provide an exceptional GoDaddy customer experience (WO

No experience needed – just bring your motivation.

In this role, you will provide an exceptional GoDaddy customer experience (WOW Experience) to every customer by giving our customers the tools and insights to help transform their ideas into successful online ventures! This will be completed through analysis of a customers account and in-the-moment

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.

No previous experience as a transportation driver, truck driver, taxi driver, courier driver or delivery driver is necessary.

No experience needed – just bring your motivation.