16 jobs found

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK's cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England. Why IQVIA? Career development opportunities to grow as we grow AI-powered career advancement through our internal talent marketplace, Career Connections Mentorship opportunities across the organisation via Employee Resource Groups Flexible working to assist work-life balance and professional success Well-being support covering your physical, mental, and financial health Awards 2026 "Glassdoor Best Place to Work in the UK" in category - 2026 Fortune World's Most Admired Companies list (for the FIFTH consecutive year!) Brandon Hall Excellence Award for Learning & Development Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team members for project execution support as appropriate Requirements Requires at least 12 months independent on-site monitoring experience of interventional studies Experience across start-up, enrolment, maintenance, close-out Digital literacy, including confidence using AI tools in a professional setting Degree in scientific discipline / health care or equivalent industry experience Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Ability to establish and maintain effective working relationships with coworkers and clients Full UK right to work required, this position is not eligible for visa sponsorship Apply today and forge a career with greater purpose, make an impact, and never stop learning! 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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK's cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South West England. Why IQVIA? Career development opportunities to grow as we grow AI-powered career advancement through our internal talent marketplace, Career Connections Mentorship opportunities across the organisation via Employee Resource Groups Flexible working to assist work-life balance and professional success Well-being support covering your physical, mental, and financial health Awards 2026 "Glassdoor Best Place to Work in the UK" in category - 2026 Fortune World's Most Admired Companies list (for the FIFTH consecutive year!) Brandon Hall Excellence Award for Learning & Development Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team members for project execution support as appropriate Requirements Requires at least 12 months independent on-site monitoring experience of interventional studies Experience across start-up, enrolment, maintenance, close-out Digital literacy, including confidence using AI tools in a professional setting Degree in scientific discipline / health care or equivalent industry experience Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Ability to establish and maintain effective working relationships with coworkers and clients Full UK right to work required, this position is not eligible for visa sponsorship Apply today and forge a career with greater purpose, make an impact, and never stop learning! 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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK's cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South West England. Why IQVIA? Career development opportunities to grow as we grow AI-powered career advancement through our internal talent marketplace, Career Connections Mentorship opportunities across the organisation via Employee Resource Groups Flexible working to assist work-life balance and professional success Well-being support covering your physical, mental, and financial health Awards 2026 "Glassdoor Best Place to Work in the UK" in category - 2026 Fortune World's Most Admired Companies list (for the FIFTH consecutive year!) Brandon Hall Excellence Award for Learning & Development Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team members for project execution support as appropriate Requirements Requires at least 12 months independent on-site monitoring experience of interventional studies Experience across start-up, enrolment, maintenance, close-out Digital literacy, including confidence using AI tools in a professional setting Degree in scientific discipline / health care or equivalent industry experience Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Ability to establish and maintain effective working relationships with coworkers and clients Full UK right to work required, this position is not eligible for visa sponsorship Apply today and forge a career with greater purpose, make an impact, and never stop learning! 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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK's cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates in South East England. Why IQVIA? Career development opportunities to grow as we grow AI-powered career advancement through our internal talent marketplace, Career Connections Mentorship opportunities across the organisation via Employee Resource Groups Flexible working to assist work-life balance and professional success Well-being support covering your physical, mental, and financial health Awards 2026 "Glassdoor Best Place to Work in the UK" in category - 2026 Fortune World's Most Admired Companies list (for the FIFTH consecutive year!) Brandon Hall Excellence Award for Learning & Development Responsibilities Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation Collaborate and liaise with study team members for project execution support as appropriate Requirements Requires at least 12 months independent on-site monitoring experience of interventional studies Experience across start-up, enrolment, maintenance, close-out Digital literacy, including confidence using AI tools in a professional setting Degree in scientific discipline / health care or equivalent industry experience Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Ability to establish and maintain effective working relationships with coworkers and clients Full UK right to work required, this position is not eligible for visa sponsorship Apply today and forge a career with greater purpose, make an impact, and never stop learning! 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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Senior Insolvency Administrator / Investigator (Progression to Assistant Manager) An established and highly regarded professional services firm is seeking an experienced Senior Insolvency Administrator or Investigator to join its growing London team. This is an excellent opportunity for a motivated individual looking to take the next step in their career, with clear and achievable progression to Assistant Manager for the right candidate. The Opportunity You will join either the Investigations or Administrations team, working on a varied and engaging caseload. The firm offers strong exposure to complex cases, allowing you to build high-quality technical experience and develop quickly within a supportive environment. Key Responsibilities Manage a portfolio of insolvency or investigation cases from start to closure Support senior staff on complex and high-profile assignments Prepare reports, statutory documentation, and case strategy analysis Liaise with creditors, directors, and other stakeholders Mentor and support junior team members where appropriate About You Strong experience within insolvency administrations or investigations Confident managing cases with minimal supervision Strong technical knowledge and attention to detail Ambitious and keen to progress into a managerial role Excellent communication and organisational skills What's On Offer Clear progression pathway to Assistant Manager Hybrid working - 3 days in the office, 2 from home A friendly, supportive, and flexible team culture Exposure to high-quality and complex casework Ongoing professional development and career support If you are looking to join a firm where your development is genuinely supported and recognised, this could be the ideal next step in your career. If this job isn't quite right for you, but you know someone who would be great at this role, why not take advantage of our referral scheme? We offer £200 in shopping vouchers for every referred candidate who we place in a role. Terms & Conditions Apply.

A well-established and highly regarded accountancy and business advisory firm in the Manchester area is looking to appoint an Insolvency Case Administrator to join its close-knit insolvency team. This is a great opportunity for someone with solid corporate insolvency experience to join a dynamic, people-focused firm where culture, collaboration, and career development genuinely matter. The firm has a long-standing presence in the North West and is known for its modern approach, strong values, and supportive working environment. You'll be joining a busy "live" team and will be expected to hit the ground running on a varied and engaging caseload. The Opportunity This role sits within the firm's core insolvency team and will involve managing cases from initial handover and appointment stage through to investigations and completion . The position offers exposure across CVLs, Administrations, and MVLs , with a particular focus on pre-appointment, appointment, and investigatory/CDDA work. You'll work alongside experienced insolvency professionals in a collaborative team that values accountability, initiative, and shared success. What's on Offer Exposure to end-to-end corporate insolvency cases , including investigations and CDDA work Opportunity to work within a busy, high-performing insolvency team Supportive and inclusive culture with strong values Hybrid working Competitive salary and benefits package Ongoing professional development and support towards insolvency qualifications Opportunity to assist with training and mentoring junior team members A firm that genuinely values its people and celebrates success What They're Looking For Proven experience in corporate insolvency Strong background in pre-appointment, appointment, and investigatory work across CVLs and administrations Ability to manage cases independently and identify billing opportunities Confidence assisting with the training and development of junior staff Strong organisational skills and meticulous attention to detail Positive, proactive attitude with strong interpersonal skills CPI qualified or working towards qualification preferred Why Apply? This is an excellent opportunity to join a forward-thinking firm that combines technical excellence with a genuinely positive culture. You'll be trusted with responsibility, supported in your development, and given the opportunity to grow within a team that values collaboration, integrity, and doing the right thing. If this job isn't quite right for you, but you know someone who would be great at this role, why not take advantage of our referral scheme? We offer £200 in shopping vouchers for every referred candidate who we place in a role. Terms & Conditions Apply.

Butler Rose are working with a well-established accountancy and business advisory firm in the North West who are looking to appoint an experienced Insolvency Case Administrator to join their busy corporate insolvency team. This is a great opportunity for someone who has solid experience across corporate insolvency case work and is confident managing cases from initial handover through to appointment stage, investigations and closure. The successful candidate will be joining a friendly, hard-working and supportive team where attention to detail, a proactive attitude and strong people skills are highly valued. THE ROLE As Insolvency Case Administrator, you will be responsible for managing a varied caseload, supporting cases across CVLs, Administrations and MVLs. You will work closely with senior team members and play an important part in ensuring cases are progressed accurately, efficiently and professionally. DUTIES WILL INCLUDE: Managing insolvency cases from initial handover through to appointment and investigation stages Working on pre-appointment, appointment and post-appointment case administration Handling investigatory work, including CDDA-related matters Supporting cases across CVLs, Administrations and MVLs Preparing case documentation and maintaining accurate records Liaising with directors, creditors and other relevant parties Supporting and assisting with the training of junior team members Working independently to progress cases and identify potential billing opportunities ARE YOU SUITABLE FOR THIS ROLE We're looking for someone with proven experience in corporate insolvency who is confident working across a varied caseload and able to hit the ground running. You will ideally have: Proven experience in corporate insolvency Strong experience across CVLs and Administrations Experience with pre-appointment, appointment and investigatory work MVL experience would be beneficial Strong attention to detail and excellent organisational skills The ability to work independently and manage your own workload A positive, team-focused attitude Confidence supporting junior members of staff CPI qualification, or working towards this, would be advantageous THE OPPORTUNITY This is an excellent opportunity to join a respected and long-standing firm with a strong presence in the North West. The team is collaborative, down-to-earth and genuinely values its people. The business offers a supportive working environment, a strong team culture and the opportunity to continue developing your career within corporate insolvency. Interested? - then please APPLY TODAY Butler Rose is committed to equality in the workplace and is an equal opportunity employer.Butler Rose Ltd is acting as an Employment Business in relation to this vacancy.

We are currently looking for an experienced and proactive individual to oversee the smooth and efficient running of large-scale clinical trials that contribute to high-quality research and impact public health and clinical practice. As Trial Manager, you will play a key role in the planning, coordination, and delivery of clinical study(s) within the CPTU. You will be responsible for coordinating participant recruitment, enrolment, and retention strategies, as well as managing site engagement and trial governance. Working closely with the wider project teams, investigators, and external partners, you will oversee trial timelines, budget adherence and regulatory compliance to ensure the study meets its objectives. To apply for this role, you will have demonstrable experience of managing clinical trials previously, and will have extensive experience of liaising with multiple stakeholders and handling protocol deviations or trial-related challenges. Strong organisational and problem-solving skills are essential. Excellent communication skills are required to provide clear updates to internal and external teams, prepare reports for funders and regulators and contribute to publications or presentations. If you are interested in applying for this exciting position, please submit your CV in the first instance (cover letters are not required). At Prospectus we invest in your journey as a candidate and are committed to supporting you with your application. We welcome all candidates to apply, regardless of age, sex/gender, disability, race, religion, sexual orientation, marital status or pregnancy/maternity. Please note this is initially a 6 month contract and will be hybrid working (East London) although some flexibility can be considered. Please only apply if you have no more than a 1 month notice period. Both part-time or full-time are considered for this role.

Line Up Aviation is recruiting for an experienced Part 145 Safety Investigator to support a busy aviation maintenance organisation on a temporary contract basis. This role will support the team with a backlog of safety reports, so applicants must have proven experience in safety reporting within an aviation environment . Previous B1 Licensed Engineer or aircraft engineering experience would be preferred. The role is ideally full-time, with a strong commitment to working through the task. The successful contractor would ideally be based in Stansted , alongside the majority of the Compliance & Safety team. Role: Part 145 Safety Investigator Location: Ideally Stansted Contract: Minimum 6 months, with review for possible extension Rate: 350 per day Hours: Ideally full-time Start: ASAP Requirements: Essential: Must have experience with safety reports / safety reporting within an aviation environment Previous B1 Licensed Engineer or aircraft engineering experience preferred Part 145 / aircraft maintenance background preferred Must be able to commit to the task, ideally on a full-time basis Ideally based in Stansted with the majority of the Compliance & Safety team Must have the right to work in the UK due to this being a contractor position Preferred: Previous B1 Licensed Engineer experience Previous aircraft engineering experience Ideally based in Stansted with the Compliance & Safety team For more information, please contact Susanne Howe-Smith at Line Up Aviation .

We are looking for an experienced Complaint Handler who is passionate about finding fair outcomes for customers. You will be loading motor finance complaints onto the system, discussing the complaint with the customer over the phone, collecting and reviewing evidence from systems to understand the situation in detail, and concluding the outcome in a final response letter. You will be joining a welcoming team within a motor finance company in Bracknell where you will have a balance of working two days in office and three days from home each week once you have passed their training program. What you'll be doing as a Complaint Handler: Taking ownership of a pipeline of complaint cases from start to resolution. Speaking to customers on the phone to discuss the complaint case and provide updates. Logging new complaints, loading customer cases onto the client system ensuring all details are entered correctly. Collecting and reviewing information from customers regarding their motor finance agreement. Taking responsibility for queries/issues through to resolution. Deciding fair outcomes for both customers and the business. Writing templated outcome letters to the customers. Managing expectations of all internal and external customers. We're looking for a Complaint Handler with: Previous experience complaint handling and complaint resolution. Previous financial services experience. Telephone experience. Confidence handling multiple workstreams. Strong attention to detail. Commutable distance to Bracknell. Hours: 37.5 hours a week Monday to Friday between the hours of 9am-5:30pm. Location: Bracknell. This can reduce to 2 days a week in office and three days from home after training and sign off. Parking: Yes Contract: 3 months initially with opportunity to extend. Training: On site full time for the first 4 - 6 weeks. This role does not offer remote working so we will not be able to consider applicants that are not within a commutable distance to Bracknell. If you're excited to join a rewarding company as a Complaints Investigator, then please click apply online and upload an updated copy of your CV. Please note any offer is subject to satisfactory pre-employment screening checks. These consist of employment, activity & GAP verification, DBS or Access NI, Credit, Sanctions & CIFAS checks. We are committed to equality of opportunity for all hires and applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships. To help you stay safe in your job search we will never ask for your bank details at the application stage . Candidate Source Ltd is an advertising agency. Once you have submitted your application it will be passed to the third party Recruiter who is responsible for processing your application. This will include holding and sharing your personal data, our legal basis for this is legitimate interest subject to your declared interest in a job. Our privacy policy can be found on our website and we can be contacted to confirm who your application has been forwarded to.

Location: On Site Pay Rate: 25.00 per hour PAYE Hours: Full Time Contract: Temporary Vehicle: Council van provided (can be kept at home overnight) Requirements: NRSWA Accreditation, Full UK Driving Licence, Business Insurance Required Desirable: Lantra Qualification Lynx Employment Services are recruiting for an experienced Street Works Inspector to support a busy Highways team. This is a fully site-based role responsible for inspecting street works and road works activities, ensuring compliance with legislation, permit conditions and safety requirements. The successful candidate will work closely with utility companies, contractors, highways teams and stakeholders to minimise disruption and maintain network safety. Key Responsibilities Conduct inspections of street works and road works, including Sample A, B and C inspections, defect inspections, investigatory inspections and Safety, Operational and Monitoring (SOM) inspections. Monitor works on site to ensure compliance with NRSWA 1991, TMA regulations and permit conditions. Issue Fixed Penalty Notices (FPNs) and Section 74 notifications where breaches or prolonged occupation of the highway are identified. Produce detailed inspection reports with supporting evidence and recommendations. Hold Joint Site Meetings with promoters and contractors to discuss defects, compliance issues and remedial actions. Investigate and respond to inspection challenges and disputes raised by utility companies and contractors. Investigate complaints from members of the public, councillors, MPs and other stakeholders relating to street works activities. Review and challenge requests for permit extensions, changes to traffic management arrangements and works durations. Support forward planning and coordination of works to minimise disruption across the highway network. Review traffic management plans, diversion routes and permit applications where required. Provide technical guidance to contractors and utility companies on street works legislation and best practice. Support licensing activities relating to skips, scaffolding, hoardings, materials and road space bookings when required. Requirements NRSWA Accreditation (essential). Experience inspecting street works and road works activities. Strong knowledge of NRSWA 1991, Traffic Management legislation and permit schemes. Experience issuing notices, managing compliance and undertaking enforcement activities. Ability to investigate defects, disputes and public complaints. Strong report writing and communication skills. Full UK Driving Licence. Business insurance for work purposes. What's on Offer? 25.00 per hour PAYE. Council van provided. Long-term opportunity within a busy highways team. Varied and autonomous field-based role. Opportunity to work on major highway and utility infrastructure projects.

Are you an experienced Financial Crime professional ready to lead and inspire a high performing team? We are supporting our client, a rapidly growing financial services organisation, in finding a talented Italian speaking Financial Crime Team Manager to strengthen their European operations. This fully remote role offers many benefits and is due to start in September 2026. If you are passionate about tackling Financial Crime, EDD, AML, Fraud, fluent in Italian, leading a team and keen to develop others, then this role offers you a fantastic opportunity to make a meaningful impact. Your responsibilities will include: Lead, support and develop a team of Financial Crime Investigators, ensuring excellence across all Financial Crime activities. Conduct quality checks and provide technical coaching to improve performance and elevate Financial Crime capability. Act as the escalation point for complex Financial Crime cases and make informed operational decisions. Foster a positive, engaged and high performing environment while acting as an effective Manager and mentor. Play a key role in recruitment activities and help shape the future of the Financial Crime team. About you: As the Financial Crime Team Manager, you will oversee a team of FinCrime investigators working across screening, transaction monitoring, escalations and related Financial Crime activities. This is an ideal role for someone with a strong background in Financial Crime screening for Fraud Detention, Regulatory Compliance, AML, Enhanced Due Dilligence EDD, KYC, Risk Assessment, Money Laundering, Embezzlement, Bribery, Corruption, Tax Evasion, Forgery and Suspicious Transactions. You will use your expertise in preventing Financial Crime, combined with your leadership experience and fluency in Italian, to coach, guide and develop your team while maintaining exceptional quality standards. Please note that the position will not offer visa sponsorship and you need to be UK based. What you get: You will be able to work remotely from the UK and the salary quoted includes an Italian language premium. Other benefits include share options, private healthcare, mental health support, EAP, wellbeing support, generous leave allowances, remote set-up contribution, monthly lunches, generous share options and gifts to celebrate events. Profile: Fluent in English and Italian, with strong written and verbal communication skills. Proven experience as a Manager within a Financial Crime function in financial services. Strong technical knowledge of AML investigations, screening processes or wider Financial Crime operations. Excellent understanding of UK and EU Financial Crime risks and the current regulatory landscape. Ability to inspire, motivate and drive performance as an established Manager of people. To apply, please send your CV in English and in Word format to Frank. languagematters is acting as an employment agency in relation to this vacancy.

Clinical Research Associate (CRA) - UK Remote Immediate start Exciting opportunity to join an innovative biotech developing next-generation therapies in the gut health space. We're looking for an experienced Clinical Research Associate to support the delivery of Phase I-III clinical studies, working closely with investigators, sites and cross-functional teams to ensure studies are delivered to the highest quality standards. You'll be responsible for: Managing clinical trial sites from start-up through to close-out Conducting SIVs, monitoring and close-out visits Ensuring ICH-GCP and protocol compliance Maintaining strong relationships with investigators and site staff Supporting patient safety, data integrity and inspection readiness Working collaboratively with Clinical Operations and external partners We're looking for: Previous CRA experience with independent site monitoring Experience conducting SIVs, IMVs and COVs Strong knowledge of ICH-GCP and clinical trial regulations Excellent communication and organisational skills CRO or biotech experience preferred This is a fantastic opportunity to join a growing organisation where you'll have genuine ownership of studies and the chance to make a real impact within an innovative clinical development programme. For more information about this opportunity, please contact Lynsey today on (phone number removed)

Technical Claims Handler Are you an experienced Technical Claims Handler with an indemnity background looking for a new position within a legal firm? Our client is an international law firm with offices in the UK, Hong Kong and Singapore who are committed to having trusted relationships, having an inclusive culture and being natural advocates for their clients. They are looking for motivated, hard-working and experienced individuals to join them as a Technical Claims Handler in Bristol City Centre. Benefits and Package for a Technical Claims Handler: Salary: Competitive Hours: 35 hours per week, 9.30am - 5.30pm Contract Type: Permanent Location: Bristol City Centre Supportive and encouraging team Working for a large and highly respected firm Workplace pension Generous annual leave allowance Key Responsibilities of a Technical Claims Handler: Handling complex technical claims cases Acting as a subject matter expert across the business Providing technical and legislative claims expertise and knowledge Instructing and collaborating with claims partners, such as brokers, lawyers, investigators and assessors Developing and managing relationships with claims partners, updating existing processes, and creating new ones Key Skills and Experience of a Technical Claims Handler: You ideally will have a strong grounding in claims including technical knowledge and experience You should be able to build internal relationships and understand the expertise across the firm Having a commercial, committed and proactive approach is required You will need to be able to interact with clients, intermediaries and suppliers to build effective, collaborative working relationships based on trust Being committed to being a part of a supportive, inclusive and collaborative firm is required If you are interested in this position and have the relevant skills and experience required, please apply now! Red Recruitment (Agency)

Daytime Healthcare are assisting a luxury private hospital in the heart of central London, who are seeking an experienced Clinical Research Nurse to join their team. They are currently seeking a proactive and enthusiastic Senior Clinical Research Nurse or Clinical Research Nurse to join our team and support participant recruitment for clinical trials in respiratory and other medical research areas. The Senior Clinical Research Nurse or Clinical Research Nurse will support in delivering clinical research by helping to set up research studies, carrying out clinical assessments, maintaining high clinical standards and adhering to protocols. Key Responsibilities: Support the delivery of clinical trials in compliance with GCP (Good Clinical Practice) and regulatory requirements. Conduct screening, enrolment, and monitoring of study participants, ensuring patient safety and protocol adherence. Perform clinical procedures such as venepuncture, ECGs, and drug administration, as required by study protocols. Assist in the collection, documentation, and accurate recording of study data in electronic case report forms (eCRFs). Collaborate with Principal Investigators (PIs), study coordinators, and multidisciplinary teams to ensure smooth study operations to ensure that the study protocol is correctly implemented and research governance standards are met and maintained Educate and support patients throughout their participation in clinical trials, addressing any concerns or queries. Maintain compliance with ethics, governance, and regulatory guidelines, including MHRA and HRA requirements. Requirements: NMC-registered nurse with experience in clinical research or a strong interest in research. Knowledge of GCP and clinical trial regulations (prior experience in a research setting preferred). Strong clinical skills, with experience in performing patient assessments and clinical procedures. Excellent communication and organisational skills, with the ability to work in a fast-paced environment. Ability to work both independently and collaboratively within a multidisciplinary team. Demonstrates ability to work under own initiative Experience in mentoring or leadership (for Senior Clinical Research Nurse applicants). Experience of working in a clinical research environment with CTIMPs is essential (for Senior Clinical Research Nurse applicants). Provide specialist knowledge, skills and experience within clinical research, and act as a resource to advise and support those involved in clinical trials at all levels (for Senior Clinical Research Nurse applicants).