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Remote position based in England. About Due to the rapid growth and expansion of business activities across multiple markets, my client is seeking an experienced, motivated, and technology-oriented individual for a full-time position as an Arabic Financial Translator (English ↔ Arabic). My client operates as a global financial services organisation supporting experienced traders across a wide range of international markets. Responsibilities The ideal candidate is a professional translator with strong expertise in economics and finance, able to work efficiently under tight deadlines in a fast-paced environment. Responsibilities include: • Translating a wide range of materials, including website content, account application and management systems, and trading platforms, • Translating client communication letters, bulletins, and announcements, • Planning and conducting research projects, including terminology extraction and use of a termbase, • Performing quality assurance on existing translations (proofreading and editing), • Document processing tasks Qualifications • Fluent Arabic speaker, • High proficiency in English, • MA or BA in Translation or a related field, • Excellent written and verbal communication skills, • Proficiency in MS Office; familiarity with CAT tools, • Minimum of three years’ relevant experience with a financial institution or in finance-related translation, • Knowledge of basic accounting concepts and a broad range of securities, • Strong time-management and organisational skills, • Self-confident, open, flexible, and able to work independently within a team-oriented environment Benefits • Career support and development, • Competitive salary based on experience, • Performance-based discretionary bonus, • Discretionary stock grant, • Group Life Assurance, • Group Income Protection, • Occupational pension scheme, • Hybrid working model, • Above-statutory annual leave, increasing with length of service, • Daily company-paid lunch and healthy snack options in the office, • Access to Private Medical Insurance, Dental Plan and/or Health Cash Plan (including dependants)*, • Corporate events, • Travel season ticket loans*

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM) Description: 18-month Contract, Inside IR35 Location: Remote, 1x a month travel to West London Rate: £430/day via umbrella engagement only The RA Training Manager - RIM will have a key role in the success of continued Veeva RIM roll-out and implementation. Supporting Organizational Change Management (OCM) training activities as a core SME and ensuring RA staff have access to fit-for-purpose training material. In alignment with the Functional Change Lead, the RA Training Manager - RIM will be responsible for the training plan creation and management, contribute to the design of training approach, prepare training materials, and organize training development; training coordination and delivery to Super Users and End Users. Major Accountabilities • Program Training Materials Development and Publishing, • Review and validate central Training material related to Veeva RIM platform deployment, • Create any local Function-specific materials as required, especially for Super Users, • Ensure training materials are regularly updated for program changes (incl. Job aids, e-learnings, etc), • Set up any mandatory e-Learning content training in Up4Growth for training push, • Training Communications, • Customize Training communications material from Central Training team to provide proactive information and regular updates, • Contribute to creating and delivering Function-specific Training communications and materials as necessary, in line with agreed central governance processes, • •Support coordination and promotion of Show & Tell/ demo sessions within Function Super User - Training Coordination, Delivery & Tracking • Attend central Train the Trainer sessions, • Align with Functional Change Lead to: Schedule Super User training sessions in Up4Growth, Deliver Training sessions, and generate Up4Growth Super User Tracking reports End User - Training Coordination & Delivery • Schedule End User Instructor-Led training sessions in Up4Growth, leveraging Function End User lists, • Deliver Training sessions, • Support Super Users during their own training sessions to End Users (tech and content support), • Provide support to End Users throughout the training period, • End User Training Records & Systems Permission Management, • Generate Up4Growth End User Tracking reports, • Track actual Attendance Report and compile End User Completion Reports, • Ensure all Function associates achieve training pass, and any other approvals required in order to secure Veeva access authorisation, • Ensure Functional business roles are correctly mapped to correct system roles and permissions Stakeholder Management & Engagement: • Help to raise Functional Training-related risks, issues, and change requests as required via appropriate channels, ensuring Central OCM team visibility, • Regularly connect with Functional stakeholders to understand and mitigate concerns Training Materials Maintenance Post Go-Live • Liaise with Veeva Product Owners to understand release impacts (x3 per year) on existing system, processes, and ways of working, • Identify key affected audiences, • Conduct impact assessment on existing training materials, • Revise, retire or create new materials and job support tools that reflect release changes, • Plan and execute training delivery strategies to key impacted audiences, • Schedule, communicate and deliver training as needed, • Evaluate training effectiveness, • Assess for effective adoption of release changes, preparing further supports, if needed Performance Indicators • Establishment of effective training strategies and delivery methods that meet end user expectations, • Documented & reported evidence of up-skilling of the RA organization on the new NRV system, • High training completion and user adoption rate at go-live, • Low number of support tickets raised related to lack of training clarity / material, • Training Satisfaction rating by Super Users and End Users Ideal Background Education: Life Science Degree or other University degree with equivalent experience Experience and skills: • Strong training, communications, project management skills, • Experience in Project management tools & systems, • Proven successful experience on the design and development of training concepts with cross-functional teams, • Strong training delivery capability, • Good understanding and direct experience with Veeva RIM deployments, • Good understanding of all RA roles, • Good Organizational awareness, • Technology-savvy – ability to leverage and use systems, technology and automation to (including digital assistants and AI tools) to derive impactful trainings and communications, • Strong communication skills For more information, please reach out to me at

Job Title: Senior Medical Writer, Clinical and Regulatory Department: Medical Writing Location: UK, Fully Remote Job Type: Initial 9 Month Contract /FTC Remuneration: Up to £80,000 This is a 9 month contract role, and you MUST be able to start this role within 4 weeks. The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documents that may include CSRs, protocols, ICFs, narratives, and IBs in a variety of therapeutic areas. Opportunities to contribute to other regulatory documents may be provided. The SMW tracks his/her own writing projects and is responsible for adhering to regulatory guidelines and department document standards. The SMW may also serve as lead for a compound and may also review the work of junior/outsourced writers, as well as review CSR-related documents (Statistical Analysis Plans, TFLs) to help ensure appropriate content for inclusion. JOB RESPONSIBILITIES: • Works with the clinical team, to write the content of clinical documents that may include CSRs, protocols, ICFs, narratives and IBs in a variety of therapeutic areas. Opportunities to write or contribute to other Regulatory documents may be provided, • Represents MW at meetings, • Drives document development meetings, • Articulates document strategy and timelines, • Identifies the appropriate parties for a document content decision, and if a discussion is faltering, bring the discussion back on track with minimal fuss, • Follows discussions to their conclusion, synthesizes the message, and presents clear accurate prose quickly, • Participates in process improvement initiatives, working groups, etc. within MW and throughout Global Development, • Manages processes and organizes priorities; solves problems; fosters collaboration to resolves conflict, • May review the work of junior and outsourced MWs, • May review CSR-related documents (Statistical Analysis Plans, TFLs) to help ensure appropriate content for inclusion, • Writes in plain language style as appropriate (eg, for ICFs), • Explains complex medical/scientific concepts (such as medical procedures, clinical study design, and drug mechanisms) to a lay or patient audience, • May mentor junior staff, • Ensures adherence to applicable guidelines, templates and SOPs for all MW documents provided for therapeutic area, • Remains compliant with internal training JOB REQUIREMENTS: Education • Bachelor's degree (advanced degree preferred) Experience • Minimum of 3 years of relevant MW experience including working knowledge of biostatistics., • Strong knowledge of the clinical research process and regulations/guidelines, • Clinical document reading, writing, and editing experience, • Strong organizational, interpersonal and communication skills, • Strong knowledge of MS WORD, Adobe Acrobat, PowerPoint, and electronic document management systems, • Ability to manage multiple projects, • Familiarity with ICH GCP guidelines For more information, please reach out to You MUST be UK-based and hold the Full Right to Work

Job Title: Senior Manager, Regulatory Labelling Location: UK, Fully Remote Salary: Competitive Salary + Excellent Benefits Employee Type: Permanent As a Senior Manager, Regulatory Labelling, you will take leadership on everything related to Regulatory Labelling. This includes inputting from a regulatory labelling perspective on developing and established drug programs and being accountable for driving global labelling strategies. This is a challenging opportunity to demonstrate your knowledge in managing regulatory processes and supporting cross-functional teams with end-to-end labelling processes. Responsibilities: • Support end-to-end labelling processes including driving labelling strategies for both development programs and established drugs and oversee all operational labelling activities., • Be responsible for executing and effective quality control reviews and tracking (primarily) internally used labeling documents (Core Data Sheet, Core Patient Information Leaflet, Core Instructions for Use) and outward facing local/regional labeling (EU SmPC, EU PIL, etc) as well as container and carton labels to meet regional regulatory requirements and ensure consistency between labeling, labels and supportive documents., • Act as operational expert for the Global Labeling tracking in RIMs, ensure development and maintenance of templates, collaboration features and system upgrades., • Contribute to the continuous improvement of the end-to-end labeling process including excellent proofreading/editing skills and compiling supportive documentation., • Support labeling inspection/audit readiness activities., • Conduct international labeling operations activities to support global new product and supplemental applications to product registration, and post approval launches for impacted international markets., • Collaborate with Technical Operations team members to ensure commercial distribution, Regulatory Technology for labeling submissions, PV for safety reporting, and other functional groups. Provide labeling to Advertising and Promotion for marketing pieces, and with Commercial for website postings if needed., • Work with Regulatory Operations, Regulatory Affairs, Tech Ops, etc. for labeling distribution, tracking and quality control., • Utilize regulatory/product knowledge to provide operational support to ensure that labeling materials meet regulatory and company requirements and timelines. Skills and Experience: • University Degree in a scientific degree., • Experienced in the following, CCDS, PIL, USPI, Target label profiles., • 5+ years of experience in drug development especially in labelling, product package coordination, clinical supplies/packaging, supply chain regulatory affairs, or quality., • Good working knowledge of key labeling regulations/guidance and past experience in label development, • The ability to research and create comparator labeling documents, • Electronic document management systems use and / or electronic submission experience, • Solid understanding of requirements for tracking of labeling updates. Understanding of label development and submission processes preferred., • Solid aptitude for use of IT systems; Regulatory Information Management System (RIMS), electronic document management system (EDMS). Ability to manage the review and approval of labeling in a document management system., • The ideal candidate should be action oriented, customer focused, ability to manage workloads and set priorities. In addition, he/she should be capable of dealing with ambiguity, be creative, be comfortable working with multifunctional teams, • Fluent in English written and spoken To be considered for this position, you must be based in the following locations: UK, Spain, Germany, or Bulgaria. Please note this role does not offer sponsorship and the right candidate must hold the Full Right to Work. For more information, please contact

Job Title: Regulatory Affairs Training Manager – Regulatory Information Management (RIM).Description: 18-month Contract, Inside IR35.Location: Remote, 1x a month travel to West London.Rate: £430/day via umbrella engagement only.The RA Training Manager - RIM will have a key role in the success of

Children’s Home — Registered Manager (South region).Relocation support available for those willing to relocate.We are seeking an enthusiastic and determined Registered Manager to lead a residential children’s home.The successful candidate will head up a team, ensuring that children receive out

Remote position based in England.Due to the rapid growth and expansion of business activities across multiple markets,.Arabic Financial Translator (English ↔ Arabic).My client operates as a global financial services organisation supporting experienced traders across a wide range of international m

Job Title: Senior Medical Writer, Clinical and Regulatory.Job Type: Initial 9 Month Contract /FTC.This is a 9 month contract role, and you MUST be able to start this role within 4 weeks.The Senior Medical Writer (SMW) works with team members and independently to write the content of clinical documen

Why work with Cpl UK Healthcare?. Cpl UK Healthcare are a market-leader in recruiting AHP’s across the UK.

Senior Manager, Regulatory Labelling.Competitive Salary + Excellent Benefits.As a Senior Manager, Regulatory Labelling,.This includes inputting from a regulatory labelling perspective on developing and established drug programs and being accountable for driving global labelling strategies.This is a

Children’s Home — Registered Manager (South region).Relocation support available for those willing to relocate.We are seeking an enthusiastic and determined Registered Manager to lead a residential children’s home.The successful candidate will head up a team, ensuring that children

Technical Sales Manager – Imaging & Detector Systems - £70,000 + 20% bonus.A growing specialist imaging and detector systems company is seeking a.This role is ideal for someone with strong technical understanding (imaging, detectors, physics, engineering) and the commercial ambition to progress i

Why work with Cpl UK Healthcare?. Cpl UK Healthcare are a market-leader in recruiting AHP’s across the UK.

Our Client is hiring an experienced Packaging Engineering Project Manager to join their world-class manufacturing site in Cramlington, Northumberland.In this pivotal role, you will lead the delivery of advanced packaging solutions—driving and leading the design, installation, and commissioning of

CPL Executive Search has been retained as the exclusive search and selection (recruitment) company to look for a strong and passionate results orientated leader, with good strategic vision to lead the global activities for our Client’s Natural Food Ingredients business unit. Please note that CPL E

Deputy Medical Director – Surgical Services (South Coast Region).An experienced medical leader to join the senior management team of a leading independent healthcare provider, overseeing surgical services across two high-performing South Coast sites.Part-Time (4–5 days per week) and flexible to

Regulatory Affairs Manager/Snr Manager - UK Market.Hertfordshire, UK – Hybrid, 3x a week on site.This is an excellent opportunity to join a leading pharmaceutical business.In this position, you will be responsible for all aspects of the UK product portfolio for developing drugs and established pro

Remote position based in England.Due to the rapid growth and expansion of business activities across multiple markets, my client is seeking an experienced, motivated, and technology-oriented individual for a full-time position as an Arabic Financial Translator (English Arabic).My client operates

Technical Sales Manager – Imaging & Detector Systems - £70,000 + 20% bonus.A growing specialist imaging and detector systems company is seeking a.This role is ideal for someone with strong technical understanding (imaging, detectors, physics, engineering) and the commercial ambition to progress i

Sales Territory Business Manager.Location: Southwest England & Wales.The Immunology Territory Business Manager (TBM) will be responsible for managing the business for biologic in key accounts within their territory.TBMs will lead on local account planning across priority hospital accounts and the ov