Trabajos investigator en Reino Unido

Large Housing Association requires a Complaints Investigator to analyse and resolve complaints in a fair and impartial manner. With a sound understanding of the regulatory timescales and deadlines associated with complaint resolution, you will be required to take case ownership and conduct a comprehensive investigation using all available information and documentation. You will be expected to provide excellent customer service when interacting with complainants either in the form of correspondence, phone or at the office, adhering to our service standards and meeting the diverse needs of the customer. Experience of responding to Stage 1 complaints is vital and experience of handling Stage 2 would be beneficial. Based in Hammersmith - hybrid working with Wednesday and Thursday in the office. • You will demonstrate a personal commitment and responsibility for providing a highly resolution-based service, aiming to resolve complaints at the first stage., • You will acknowledge and resolve complaints by project managing high quality responses., • You will take ownership of a complaint from start to closure, ensuring that the customer is regularly kept informed of progress., • Ensure complaints are responded to in a timely and customer friendly way considering the needs of the individual residents., • Solve complex open and ongoing complaints., • Prepare comprehensive papers for stage 2 reviews using a pro-active approach, providing expert guidance around the complaint details to aid swift resolution., • Provide high level written responses in line with the understanding of a regulatory approach to complaint handling., • Ensure that all compensation payments are processed and issued to complainants in adherence with our service standards.

Temporary Complaints Officer (Housing Needs) – Wembley Hybrid | 36 hours per week | £23.81 PAYE / £31.35 Umbrella | Immediate Start | Until October (possible extension) Are you a customer-centric superstar with a passion for resolving housing-related issues? We’re looking for an experienced Complaints Officer to help clear a backlog of Stage 1 complaints covering housing needs, homelessness, and temporary accommodation. What You’ll Be Doing Investigating Stage 1 complaints Working closely with the Housing Needs team to produce high-quality written responses Delivering fair, evidence-based outcomes Ensuring a compassionate, resident-focused approach Who We’re Looking For We’d love to hear from applicants with: Local Authority experience Homelessness & housing complaints expertise Housing Ombudsman experience (advantageous!) Awareness of key legislation: • Housing Act 1996 Part VII, • Homelessness Reduction Act 2018 Location: Wembley Hybrid: 3 days a week in the office (Monday = mandatory) 36 hours per week Contract: Until October, with potential to extend Start Date IMMEDIATE – temp booking

Fleet Contract Manager | Kent/London (Hybrid) | up to £60,000 | Permanent The Opportunity Are you a technical engineer with a sharp eye for detail, looking to transition from the "shop floor" to the boardroom? We are partnering with a major rail operator to find two Fleet Contract Managers who possess a unique blend of engineering "DNA" and commercial curiosity. This isn't your standard legal-heavy procurement role. Instead, we are looking for technical authorities who can bridge the gap between complex engineering investigations and the contractual frameworks that govern them. You will act as a trusted advisor, translating fleet performance data and technical modifications into robust commercial agreements (ROSCO leases and side letters). If you are looking for a role where you can put your "stamp" on a function and lead the evolution of a fleet, this is it. Responsibilities * Engineering-Led Contract Management: Negotiate and review Rolling Stock leases and maintenance amendments through a "technical lens" to ensure fleet performance objectives are met. * Commercial Relationship Management: Act as the primary commercial link between the business, ROSCOs, and engineering suppliers. * Technical Investigations: Collaborate with Engineering Managers to identify risks and opportunities, translating technical issues into contractual outputs. * Asset Management Support: Advise on contractual frameworks, warranties, and performance regimes to protect the business's assets. * Financial Control: Manage Oracle purchase requisitions and sales orders, ensuring rigorous financial oversight of engineering contracts. * Project Leadership: Provide commercial expertise to wider company modification projects, justifying business cases for new requirements. The Candidate We are seeking individuals with an "Engineering First" mindset. You don't need to be a lawyer, our client can teach you the complex legalities, but you must have the technical authority to challenge what "looks off" from an engineering perspective. * Technical Foundation: A strong mechanical engineering background is essential. You should be IMechE accredited or actively working towards it. * The "Technical Investigator": Experience in writing technical reports, managing fleet modification documentation, and conducting investigations is vital. * The "Contractual Lens": You possess the confidence to interrogate a contract to ensure it reflects the technical reality of the fleet. * Interpersonal Agility: You are as comfortable discussing engineering schematics with technicians as you are presenting a commercial business case to the Board. Location Ford & Stanley TalentWise - Business specialising in blue collar trade & technical services - permanent and temporary. * Ford & Stanley Recruitment - Business specialising in white collar spanning all company functions with specialist verticals within Digital, Rail Engineering, Civils & Infrastructure, General Manufacturing, Supply Chain & Logistics both permanent and contract.

Company description Stats Perform is the market leader in sports tech. We provide the most trusted sports data to some of the world's biggest organizations, across sports, media, and broadcasting. Through the latest AI technologies and machine learning, we combine decades' worth of data with the latest in-game happenings. We then offer coaches, teams, professional bodies, and media channels around ... ZIPC1_UKTJ

Senior Clinical Research Associate | London, UK | 6-Month Contract (Full-time) HYBRID Key responsibilities • Support the day-to-day operational delivery of Phase I–III clinical trials across multiple complex indications, • Maintain and oversee Trial Master File (TMF) quality and completeness to ensure inspection readiness, • Assist with study start-up activities including site documentation collection, regulatory submissions and site activation support, • Coordinate trial documentation, vendor communications and study tracking to support global clinical operations teams, • Collaborate with Clinical Trial Managers, CRAs, regulatory teams and external partners to ensure timely study execution, • Track study milestones, manage essential documents and support reporting across clinical programs, • Assist with preparation and management of study materials including investigator meeting documentation and training materials, • Support audit and inspection readiness activities and ensure compliance with ICH-GCP and internal procedures Candidate requirements • Minimum 5 years’ experience as a Clinical Trial Associate or within a comparable clinical operations role, • Strong experience supporting Phase I–III clinical trials, • Experience working within biotechnology environments, ideally supporting innovative or complex therapeutic programs such as cell or gene therapy, • Exposure to multiple complex therapeutic areas and global clinical trial operations, • Strong understanding of clinical trial documentation, TMF management and regulatory processes, • Excellent organisational skills with the ability to manage multiple studies and priorities simultaneously, • Strong communication skills and ability to work effectively within cross-functional clinical teams What is offered • Opportunity to work within an innovative cell therapy biotech environment, • Exposure to cutting-edge clinical development programs, • Hybrid working model in London, • 6-month fixed term contract.

🚀 Head of Clinical Operations | Gene Therapy We’re partnering with an exciting gene therapy company that has recently secured £50,000,000 in funding to accelerate its next phase of growth. With a cutting-edge AAV-based platform targeting both CNS and systemic diseases, this company is advancing potentially curative therapies across multiple indications. This is a rare opportunity to join at a pivotal moment and lead the clinical strategy from early-stage through to late-phase development. You will: • Lead and scale the Clinical Operations function globally, • Drive execution of first-in-human and later-stage gene therapy trials, • Oversee CROs, vendors, and international investigator sites, • Build and implement clinical development operational strategy, • Partner closely with Clinical, Regulatory, CMC, and Translational teams 🎯 What We’re Looking For • Significant leadership experience in Clinical Operations (biotech/pharma), • Strong background in gene therapy, rare disease, or CNS trials, • Proven delivery of early-phase and/or registrational studies, • Deep understanding of global clinical trial execution, • A hands-on leader who thrives in a high-growth, fast-paced environment 🌍 Why Join? • Recently funded with £50M—strong runway and momentum, • Innovative platform with broad therapeutic potential (brain and beyond), • Opportunity to shape and build a world-class clinical function, • Work on therapies with the potential to transform patients’ lives

Complaints Investigator \n\nHourly Rate: £23.81 PAYE OR £31.35 Umbrella\nLocation: Wembley, HA9 - Hybrid working (3 days onside)\nJob Type: Temporary (until October 2026 with possible extension)We are seeking a skilled Complaints Investigator with extensive experience in handling complex complaints, particularly in the areas of housing, repairs, homelessness, and public realm issues. This role requires managing stage 1 complaints and drafting responses on behalf of senior stakeholders, necessitating a blend of tact, diplomacy, and tenacity to ensure thorough investigations and resolutions.\n\nDay-to-day of the role:\n\nHandle and investigate stage 1 complaints across various domains including housing, repairs, homelessness, and public realm.\nDraft and prepare response documents on behalf of Corporate Directors, ensuring accuracy and appropriateness of the content.\nInteract and communicate effectively with senior stakeholders to gather necessary information and feedback for complaint resolution.\nFollow through on investigations diligently, ensuring all aspects are thoroughly explored and resolved.\nMaintain high standards of documentation and record-keeping throughout the complaint handling process.Required Skills & Qualifications:\n\nProven experience within Local Authority & homelessness complaints handling\nExperience managing stage 1 complaints and preparing executive-level correspondence.\nStrong ability to interact with and influence senior stakeholders.\nExcellent written and verbal communication skills, with a focus on tact and diplomacy.\nDemonstrable tenacity in following through on investigations to ensure resolution.\nAbility to work independently and as part of a team in a dynamic environment.To apply for the Complaints Investigator position, please submit your CV your relevant experience

About the Citrin Foundation The Citrin Foundation is a dynamic, forward-thinking organisation focused on pioneering innovative research and supporting patients with citrin deficiency. We fund research projects to better understand the condition and develop new therapies. We also provide support to citrin deficiency patients and their families globally. By collaborating with leading institutions, clinicians, and researchers worldwide, we drive impactful change through our research efforts, clinical programmes, patient engagement, and advocacy efforts. Find out more about us: Role Summary We are seeking a highly skilled and motivated Research Programme Manager to drive our global research portfolio that spans basic and translational research through to clinical studies and therapy development. This role is both strategic and hands-on. The postholder will connect scientific discovery to therapeutic application in partnership with a global consortium of scientific and clinical leaders. This is a fantastic opportunity for an early-career translational science professional such as a recent post-doc to move beyond singular research projects and take ownership of research operations and patient-centred solutions in the rare disease space. The Foundation operates as the hub in the entire translation pathway. You will gain a unique perspective of the entire drug development journey and serve as a vital contributor every step of the way. Come join us and make a tangible difference in the rare disease community. Key Responsibilities 1. Research and project management • Manage Foundation-funded research projects, monitoring study progress, budgets, and milestones to ensure alignment with our core objectives., • Serve as primary liaison between academic investigators, clinical collaborators and industry partners. 2. Translational strategy and operations • Identify and evaluate new research opportunities with high translational potential., • Support both Foundation initiatives and projects led by our consortium of investigators in navigating logistical, operational, and regulatory hurdles to accelerate the translation from lab to clinic. 3. Clinical and regulatory support • Support the planning and operational management of natural history studies., • Collaborate with our patient engagement team to ensure that studies are patient-focused and data-driven, informing future clinical development and study designs. 4. Stakeholder Advocacy • Foster collaboration across a multi-disciplinary network of scientists, clinicians, and patient families., • Communicate complex scientific findings in a clear, impactful way to internal and external stakeholders, our patient community, and the public. About You Essential Skills and Experience • PhD or equivalent experience in biomedical sciences or a related field., • A good understanding of basic and translational research, research operations, or clinical study designs., • Critical thinker with strong problem-solving ability., • Strong organisational skills and ability to manage multiple complex projects and competing priorities while maintaining a high level of operational detail., • Exceptional written and verbal communication skills, engaging confidently with both leading experts and lay stakeholders., • An adaptable, entrepreneurial and “can-do” mindset, working both collaboratively and independently in a lean multi-disciplinary team., • Patient-centred, empathetic, and discreet, with a deep commitment to the mission of improving outcomes in the rare disease space. Desirable • Experience in early-phase studies or investigator-led clinical trials is strongly preferred., • Experience in rare diseases or metabolic conditions., • Established track record of peer-reviewed publications or conference presentations., • Keen interest in basic and translational science for medical conditions., • Experience working in a charity, foundation, or multi-stakeholder environment.

Housing Complaints / Resolutions Officer Role \n\nHousing Solutions \n\nResponsible for the handling of customer complaints, member and MP enquiries, statutory enquiries\n\nCity of London\n\nHybrid Working \n\nStage 2 Complaints£28ph Umbrella \n\n3 month contract to start ASAP - extension possible\n\nWe have a fantastic new job opportunity for a Stage 2 Complaints Investigator / Escalation Caseworker with previous experience of investigation and resolution of complex and multi-faceted complaints, exceptional customer service skills and excellent verbal and written communication skills.\n\nWorking as the Stage 2 Complaints Investigator / Escalation Caseworker you will be part of a dedicated Complaints division and will be tasked with investigating and resolving all Stage 2 complaints, in a fair & impartial manner.\n\nAs the Stage 2 Complaints Investigator / Escalation Caseworker you will have a sound understanding of the regulatory timescales, and deadlines, associated with complex complaint resolution, and will be required to take case ownership (until resolution) and conduct a comprehensive investigation, using all available information and documentation, including leading case reviews of the complaint process at Stage 1.\n\nDUTIES\n\nYour duties as a Stage 2 Complaints Investigator / Escalation Caseworker will include:\n\nProvide excellent customer service when interacting with complainants either in the form of correspondence, phone or at the office, adhering to the service standards and meeting the diverse needs of the customer\nDemonstrate a personal commitment and responsibility for providing a highly resolution-based service, understanding that Stage 2 is the final stage for resolution\nAcknowledge and resolve complaints by leading on high quality responses\nTake ownership of a complaint from start to closure, ensuring that the customer is regularly kept informed of progressKey skills:\n\nHandling large case loads \n\nLiaising with Solicitors/Contractor's \n\nAccountable for the accuracy and completeness of your work, remaining calm under pressure, making informed and reasonable decisions.\n\nExcellent complaint handling and communication skills and actively seek to improve working practices and customer service.\n\nTake responsibility for your own learning and development\n\nExcellent PC skills including Microsoft Word and Excel\n\nExcellent verbal and writing skills

Who We Are Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth largest specialty generic pharmaceutical company in the world with global revenues of US$6 billion. Supported by more than 40 manufacturing facilities and more than 40.000 employees around the globe, we provide high-quality, affordable medicines, trusted by healthcare professionals and patients, to more than 100 countries across the globe. Over the last two decades, Sun Pharma has established itself as a leading player in the generics market, and are rapidly ramping up their presence in the specialty branded market with a focus on dermatology, ophthalmology and onco-dermatology. Values At Sun Pharma our core values—Humility, Integrity, Passion, and Innovation—are part of our unique culture, known as Sunology. We are empowering our employees to create their “Own Sunshine”. We believe in being Better Everyday by investing on lifelong learning, Taking Charge by owning our impact, and Thriving Together in a workplace where collaboration is encouraged. We are committed to being an inclusive and equitable employer, valuing diverse perspectives and creating an environment where all individuals feel respected, heard, and inspired to bring their best selves to work. Overall Job Purpose The Medical Manager Ophthalmology (MM) is responsible for leading Medical Affairs activities in the UK for a branded Ophthalmology product in the post‑launch phase. In alignment with the Brand Strategy and medical Plan, the MM works closely with UK Key Opinion Leaders (KOLs) to drive scientific engagement and ensure high‑quality medical support. Key responsibilities include initiating and managing clinical research projects, organizing national advisory boards, and delivering scientific publications, congress posters, and presentations in collaboration with KOLs. As the medical expert for the product, the MM provides medical and scientific education to KOLs and field colleagues through presentations, training, and ongoing scientific support. The MM also develops medical content and provides strategic briefings for KOLs attending congresses. In addition, the MM partners closely with the Marketing Manager, offering medical insights and content to support marketing materials and projects, while ensuring strict adherence to pharmaceutical industry codes and compliance standards. Major tasks & responsibilities (70% field) Strategic plan development in close collaboration with Marketing and Head Medical Affairs Execution of the Medical Affairs launch strategy plan at country level. • Mapping and management of KOLs on the disease, • Develop links with and support national networks in the therapeutic area, • In collaboration with Market Access, ensure product Access and in local guidelines, • Organizing local Advisory Boards (content, objectives, speakers, attendees), • Local publications and congress posters within strategy of the product, • First medical HCP contact at Congresses and symposia,, • Content input, providing medical slide decks, briefing KOLs for congress and symposia presentations, within brand strategy, • Medical information on requests to HCPs and medical Presentations to HCPs within Brand strategy, • Handling Investigator-Initiated trials (IIT): Internal approval and contracting, • Approval of contracts for external (consultancy/speaker) activities with HCPs, • Develop medical training decks and give medical training for commercial colleagues in the field on disease and product, • Medical scientific and strategic input on Marketing projects and materials in collaboration with Marketing Manager, • Ensure all Medical and Marketing projects, materials and presentations are compliant to pharmaceutical codes. Education Qualifications • (Bio) medical (scientific) academic degree, • Training in the code of Pharmaceutical Compliance rules, • Presentation and training skills Work experience • Minimum of five years of Medical Affairs experience in the pharmaceutical industry, • Ophthalmology network and experience, • Strategic and operational experience in launch activities, • Experience in Marketing and or Commercial function in Pharmaceutical Industry Technical skills/job specific competencies • Mandatory - Fluent in English, • Setting up and run Medical projects, • Good developed influential skills use internally and internationally in the medical field, • Outgoing personality, likes to interact with people, being in the field, • Goal oriented and strategic thinking, • Good understanding of pharmaceutical industry codes, • Good collaboration with Marketing and Sales colleagues, • Good sense of the Brand strategy and follow up in all projects, • Good teaching and presentation skills, • Flexibility and patience, • Positive creative mindset to challenges Accountability • Takes responsibility and owns up to all activities and personal actions, • Executes with agility, without compromising on core values, • Follows through and implements agreed decisions within agreed timelines consistently, • Takes responsibility for personal and team actions, and learns from part mistakes, • Clearly defines accountability within the team and drives them to achieve high performance standards Collaboration • Builds strong internal networks and communicates across departments and functions to meet business objectives, • Proactively contributes to the success of other departments and shares credit., • Does not hesitate to seek help, • Focuses on overall business value to Sun over own department/function, • Is culturally sensitive and comfortable working in a global context Customer Centricity • Understands and responds to customer/ stakeholder needs, • Develops positive long-term relationships with customers/ stakeholders, • Displays an entrepreneurial mind-set and identifies opportunities and ways to stay ahead of competition

This is a hands-on contract inside a high-performing cyber engineering function, focused on delivering real, tangible improvements to Insider Risk capabilities through Microsoft Purview. Design and deliver integrations into Microsoft Purview to enhance Insider Risk capability.

Investigate serious concerns about Health and Care professionals, assess risk and make evidence-based decisions to protect the public whilst managing a varied caseload of Registrant fitness to practise complaints.

This is a hands-on contract inside a high-performing cyber engineering function, focused on delivering real, tangible improvements to Insider Risk capabilities through Microsoft Purview. Design and deliver integrations into Microsoft Purview to enhance Insider Risk capability.

Fraud Investigator Location: Lambeth Town Hall - Hybrid (4 days remote working, 1 day office work per week) Contract: 6 month contract Hours: 35 hours per week (Monday-Friday) Pay Rate: £26.Umbrella About the Role: Lambeth Council is seeking an expe

Large Housing Association requires a Complaints Investigator to analyse and resolve complaints in a fair and impartial manner.With a sound understanding of the regulatory timescales and deadlines associated with complaint resolution, you will be required to take case ownership and conduct a comprehe

If you are a current Jazz employee please apply via the Internal Career site. Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit for more information. Brief Description: The Global Study Leader (GSL) leads global Phase I–IV clinical trials, overseeing strategy, execution and cross-functional alignment. They manage vendors, budgets, timelines, and documentation and serve as a Subject Matter Expert (SME) in audits, process design, and team leadership, ensuring Good Clinical Practice (GCP) compliance and operational excellence across studies. Essential Functions/Responsibilities - In partnership with the study team and internal and external service providers, provides oversight to ensure study delivery and ensure operational excellence. - Delegate tasks to study team members as appropriate. - Lead implementation, execution and management of global Phase I–IV clinical trials. - Lead, facilitate and delegate trial-related meetings, ensuring alignment with cross-functional teams. - Act as a primary point of escalation for cross-functional stakeholders for timely issue resolution and alignment. - Participate in program-level discussions (FMT, GPT), providing clear and timely updates to senior management (as needed). - Develop and execute clinical trial strategies in collaboration with cross-functional teams during the trial lifecycle including tracking and reporting trial progress, risks and mitigation strategies to senior leadership. - Hold overall accountability for the Trial Master File (TMF). Acts as an SME for Clinical Operations related sections. - Lead the development and review of trial—specific plans and essential clinical trial documents. - Review and approve key trial documents including protocols, informed consent forms, monitoring plans, and Clinical Study Reports (CSRs) in line with Standard Operating Procedures (SOPs). - Actively contributes to the operational oversight and strategic direction of assigned studies, including feasibility assessments, planning, vendor selection, patient recruitment strategies, and financial forecasting. - Contribute to the planning and conduct of Investigator Meetings, including driving meeting preparation, presenting trial materials, and supporting effective delivery of key messages. - Identify, assess, and proactively manage risk and contingencies to safeguard timelines, quality and compliance. - Develop, manage and track trial timelines and budgets, in line with projected spend. Estimate, track and critically analyze vendor financial spend on trials. - Accountable for the oversight and management of external service providers and vendors to ensure quality, compliance, and performance. - Oversee trial tracking activities and ensure accurate, timely updates within trial management systems. - Accountable for final approval and oversight of trial documentation archiving in compliance with regulatory and company requirements. - Serves as trial lead and SME during audits and inspections. - Coordinate Investigational Medicinal Product (IMP) shipment authorization with regulatory and clinical supplies functions. - Assist and support data query process. - Perform monitoring visit report review (as required). - Lead and participate in Clinical Operations / Global Clinical Development Operations (GCDO) initiatives (as assigned). - Serves as a Clinical Operations SME in the design and review of processes. - Ensure trial activities are conducted according to GCP and relevant SOPs and in accordance with the agreed timelines and trial protocol. - Leadership / People Management Responsibilities: - Mentor and coach Global Study Managers (GSMs) Clinical Research Associates (CRAs), and Global Study Associates (GSAs) to support professional development. - Lead Clinical Trial Working Groups (CTWGs). - Provide leadership in resolving complex trial issues and escalating risks appropriately. - Manage and maintain high performing clinical teams. Required Knowledge, Skills, and Abilities - Clinical research experience, with proven global trial management and portfolio-level oversight with experience in clinical operations leadership roles. - Excellent organizational skills, time-management and attention to detail. - Excellent written and verbal communication skills and stakeholder management abilities. - Ability to work both independently and collaboratively in a fast-paced environment. - Proficiency in Microsoft Office (Word, Excel, Outlook, PowerPoint). - Experience with and strong knowledge of Clinical Trial electronic systems (e.g., TMF, Clinical Trial Management System (CTMS), etc.). - Strong knowledge of clinical trial processes, ICH-GCP, and regulatory requirements. - Strong knowledge of regulatory start up process and planning in support of Study Start-Up (SSU). - Proven track record of effectively managing in a cross-functional environment. - Excellent project management skills with a proven track record of managing global, multi-center clinical trials. - Strong leadership and governance experience; ability to influence at senior levels. Required/Preferred Education and Licenses - Bachelor’s degree, preferably in life sciences, healthcare, or a related field, or equivalent experience. - Advanced degree preferred. #LI-SM1 #LI-remote Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLY Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $145,600.00 - $218,400.00 Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidates expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis. At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Companys Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazzs Long Term Equity Incentive Plan. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: .

Major Crime Staff Investigator needed in Sleaford, £23.

Provide Medical Safety/PV inputs to the assigned products at Jazz Pharmaceuticals, which may include Clinical Development program of all phases, Investigator Sponsored, Compassionate Use, and Disease Monitoring Programs; liaise with Clinical Sciences, Clinical Operations, Medical Affairs, Biometrics

The Sub Investigator has responsibility for the clinical safety of the patients partaking in the clinical trial, collecting and recording accurate clinical data while ensuring that the well‑being and interests of the subjects enrolled in the studies are being met. The Sub‑I provides essential cl

Job title: Marine Investigator.

A leading insurance company is seeking a Claims Adjuster in London.The role involves investigating insurance claims, determining liability, and negotiating settlements.You will work closely with policyholders and ensure compliance with regulations.A Bachelor's degree in a relevant field and at least

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The role involves supporting investigator-initiated research activities, coordinating studies, and ensuring compliance with internal policies and regulations.

Investigation Case Manager - £21 per hr (£35 000).Investigation Case Managers urgently required for temp, fixed term and permanent contracts.The office is near Elephant & Castle.Working from home, the Case Manager is paid £21 per hr, for 35 hrs per week.The Case Manager will manage investigations

Senior Financial Crime Investigator, Retail Banking, EU (Spanish and English Speaking). Senior Financial Crime Investigator, Retail Banking, EU (Spanish and English Speaking). Senior Financial Crime Investigator, Retail Banking, EU (Spanish and English Speaking).

The Senior Clinical Study Manager (Sr. Coordinate production of key clinical study documentation including Clinical Investigation Plan (CIP), Investigator Brochure (IB), Informed Consent Form (ICF) and Clinical Study Report (CSR). Build professional relationships with key opinion leaders and clinica

An established industry player is seeking a Senior Insolvency Investigations Administrator to join their dynamic team in London.This exciting role involves managing complex investigations across various sectors, focusing on fraudulent trading both domestically and internationally.The ideal candidate

Loss Prevention Investigator (or equivalent) preferred. The Asset Protection Specialist (APS) is primarily responsible for preventing financial loss caused by theft and fraud, organized retail crime and supporting safety and environmental program compliance in their assigned store(s). The APS will d

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If you are an Italian speaking Financial Crime Investigator with expertise in regulations, fraud detection and investigative techniques, then we are looking for you.In this Italian speaking FinCrime role you will be passionate about protecting financial integrity, driving operational excellence and

Additionally, you will manage customer accounts, respond to their requests and queries, schedule regular calls and meetings, and provide consultancy to help them develop and implement successful brand protection strategies. As a global leader in Trademark and Brand Protection, we partner with busine

They are currently seeking a CRA / Clinical Research Associate in London. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedure

A clinical research organization in Romford seeks a Sub Investigator responsible for ensuring patient safety in clinical trials, managing study teams, and communicating with various stakeholders.

A recruitment agency is seeking a Senior Analyst for Investigations and Asset Tracing in London.The role involves asset recovery, research for activist investments, and strategic corporate development while managing complex, long-term projects across jurisdictions.Ideal candidates have strong organi

Job title: Marine Investigator.

A well-established Local Authority in the South Coast is seeking an experienced Trading Standards Officer for a 6-month contract with hybrid working.The ideal candidate will manage a varied Trading Standards caseload, dealing with enforcement legislation, consumer protection, and compliance issues.R

A local council in England seeks an Environmental Health Officer to investigate complaints and enforce health-related legislation.The ideal candidate will have a degree in Environmental Health and relevant experience.Responsibilities include managing public health duties, inspecting caravans, and en

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