Company Detail

Cpl Life Sciences
Member Since,
Login to View contact details
Login

About Company

Job Openings

  • Overview Our client who is developing an advanced and innovative wound... Read More
    Overview Our client who is developing an advanced and innovative wound dressing platform (Advanced Tissue Repair Platform) to substantially, will improve the clinical outcome for patients with Chronic and Complex Wounds whilst maintaining simplicity for care providers. Our Client is on a mission to improve the current standard of care to reduce the physical and psychological impact of poor wound healing on patients that suffer from these wounds. Our clients team is small, so this role will have high risibility within the company so a chance to shine and be rewarded. Our client prides themselves on being a pragmatic, a lean start-up that’s driven to deliver world-changing technologies at pace and responding to challenges flexibly and rapidly. Proud of their company values and live them every day: JOB SUMMARY The Quality Assurance and Regulatory Affairs Director will be responsible for developing, implementing, and maintaining quality and regulatory systems in compliance with FDA, ISO, and other global regulatory standards. This role requires deep experience in medical device development — particularly durable medical equipment — combined with working knowledge of regenerative therapies and their evolving regulatory pathways. The ideal candidate will thrive in a fast-paced startup environment and bring strategic leadership, cross-functional collaboration, and executional excellence. ESSENTIAL RESPONSIBILITIES ⬢ Develop and maintain a robust Quality Management System (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, and applicable standards. ⬢ Lead internal and external audits, CAPA processes, non-conformance investigations, and change control. ⬢ Oversee design control, risk management (ISO 14971), and product lifecycle quality from R&D to post-market surveillance. ⬢ Establish and monitor key quality metrics and provide executive-level reporting. ⬢ Ensure supplier and contract manufacturer compliance through audits, qualification, and continuous monitoring. ⬢ Define and lead global regulatory strategy for the company’s medical device and regenerative medicine products. ⬢ Prepare and submit CE mark Technical Files, FDA submissions (510(k), IDE, PMA) and other international regulatory dossiers. ⬢ Serve as the primary regulatory liaison with notified bodies, FDA and other global regulatory authorities. ⬢ Monitor changes in the regulatory landscape (e.g., FDA, EMA, MDR) and advise leadership on compliance risks and opportunities. ⬢ Support clinical and preclinical study design from a regulatory perspective THE IDEAL CANDIDATE HAVE ⬢ A bachelor’s degree in engineering, life sciences, or a related field. ⬢ Minimum of 8-10 years of experience in QA/RA roles within the medical device industry. ⬢ Proven experience with durable medical equipment (DME) and familiarity with regenerative medicine (e.g., synthetic biodegradable polymers, HCT/Ps, combination products). ⬢ Direct experience preparing and submitting successful EU MDD and/or MDR and, FDA PMAs. ⬢ Deep understanding of ISO 13485, FDA QSR, MDSAP, EU MDR, and related standards. ⬢ A startup mentality: self-starter, hands-on, resourceful, and adaptable. ⬢ Demonstrated strong leadership and team-building abilities. ⬢ Excellent communication and cross-functional collaboration skills. ⬢ A strategic thinker mindset with attention to detail and a proactive problem-solving approach. IN RETURN OUR CLIENT OFFERS ⬢ A chance to shape the quality and regulatory foundations of a company disrupting the wound care industry. ⬢ Competitive salary and equity package. ⬢ Flexible work environment and schedule. ⬢ Opportunity for significant professional growth and leadership development. Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Senior Benefits Specialist  

    Overview Position Summary Role: Senior Benefits Specialist Duration: 1... Read More
    Overview Position Summary Role: Senior Benefits Specialist Duration: 1 x year Location: Chester (2/3 times per week in the office required) Rate: £29.12 per hour This position will be part of People Services and has responsibility for execution and administration of the benefits and retirement program, including health & welfare, savings plans, and wellness. No Direct or Indirect Reports Key Business Partners : Benefit Strategy and Governance Center of Excellence (COE) / Payroll / Strategic Benefits Delivery Management Team / Capability Center peers / HR and People Services Business Partners / Finance / Third Party Vendors and Brokers Detailed Position Responsibilities • Responsible for the effective, end to end operation of benefits programs for assigned markets, ensuring efficiency and positive customer experience • Understand, interpret, and effectively communicate benefit plan provisions, policies, programs, process and practice as the escalation point for Key Business Partners and for the resolution of Tier 2 benefits enquiries or needs • Proactively document all processes and activities, drafting and updating LWI’s (Local Work Instructions), training materials and Knowledge Articles, including defining streamlined processes for all applicable scenarios • Drive the implementation of new benefits / benefit design and process changes into operational systems, as well as undertaking process improvement activities and other projects related to benefit programs • Execute and administer day to day activities related to benefit plan eligibility, enrolments, status changes, terminations and claims, including as needed: – Liaising with system providers, local brokers and vendors – Actioning monthly changes in provider portals – Reviewing and reconciling system generated reports, data feeds and integrations – Administering invoicing and payment processes for regional and some local vendors including raising POs, validating invoice specifications and tracking payments, etc. within the defined vendor management framework – Logging, managing and monitoring through to resolution any deviations from agreed service standards – Administering some social security programs • Manage the end-to-end process for enrolment windows in partnership with benefits system provider and Benefits Strategy and Delivery Management teams, and agree and maintain annual calendars of activities • Research, problem-solve and respond on issues related to benefit programs, objectives and procedures raised by employees, HR and third-party vendors (Includes brokers, insurance providers, regulatory agencies, etc.) • Review system generated correspondence and communications, vendor websites (including benefits enrolment tools) and benefits content on the HR portal, to ensure these are current, accurate and market relevant, and support employee self-service, recommending and implementing updates as needed • Assist with compliance and governance of all total rewards plans and programs including identifying risks, participating in audits and recommending and delivering corrective actions • Collaborate with Benefits Strategy and Strategic Delivery Management teams to develop, operationalize and deliver enterprise-wide solutions • Identify and recommend opportunities for improvements in existing People Services systems and processes • Develop, specify and implement recommendations for global benefits administration systems changes, prepare change request documentation and support implementation • Manage and perform testing activities for benefits administration systems implementations, changes and ongoing enhancements • Train team members, and HRAs on benefit topics, processes and changes • Complete annual Benefit Surveys, as required • Assist with the administration of wellness programs and vendors. Coordinate wellness communications as needed Desired Experience Must have requirements: • Bachelor’s degree from an accredited university/college or equivalent experience • In depth experience in Benefits Administration • Demonstrated analytical abilities and attention to detail • General knowledge and understanding of HR policies, processes, regional Employment Laws and Benefits legislative requirements for the relevant region • Proficiency in Excel, particularly vlookups and pivot tables, and other Microsoft Office applications • Experience working in a rapid, fast-moving environment which is both complex and changing, together with the ability to successfully manage multiple competing tasks and priorities • Ability to use business judgment when assessing requirements and performance, in order to identify the right solution to meet business needs • Experience working in a multi-cultural/multi-country work environment • Ability to network across a global organization in order to align with organization objectives and strategy • Ability to present complex technical information in a clear and understandable way to staff, callers, and functional business and technical groups • Demonstrated continuous improvement mindset Ideal Candidates Would Also Have • Practical operational experience of other HR processes, e.g., talent acquisition, payroll, performance • Experience working within an HR Shared Services delivery model • Experience working with current HR and Benefits enabling systems: Workday, ServiceNow, Darwin, Morneau Shepell’s Ariel • Experience in coaching others to build capabilities or enhance functional depth Other Qualifications • Language Requirements: Proficiency in English required plus another European language is a plus Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Clinical Development Medical Director  

    - London
    Overview Clinical Development Medical Director – £850 per day (umbrell... Read More
    Overview Clinical Development Medical Director – £850 per day (umbrella) – 12 months A global pharmaceutical organisation specialising in Neurology is now in need of a Medical Director to oversee their clinical studies. Core skills and experience required: – · 5+ years’ experience working on Neurology studies in industry. · Experience providing clinical leadership on scientific and medical strategic input including Clinical Protocols, IDPs, CDP and Clinical Data Review. · Experience providing medical and clinical input into regulatory submissions. · Experience developing the clinical sections of the IBs, submission dossiers and responses to health authorities. · Experience supporting the PV/Safety teams on DSUR’s, PSUR’s and safety related documents. · Previously managed external stakeholders including regulatory authorities, PAGs, Ad Boards and KOLs. · Experience of moving projects from proof of conception to development decision point. · Experience training cross-functional teams on SOPs, protocols and best practice. Clinical Development Medical Director – £850 per day (umbrella) – 12 months Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Key Account Manager – South West  

    - Berkshire
    Overview Key Account Manager – Aesthetics Location: Field based — Sout... Read More
    Overview Key Account Manager – Aesthetics Location: Field based — South West England (including Hampshire, Berkshire, Wiltshire ) Employer: Global healthcare company The opportunity Join a growing aesthetics business with a premium, clinically backed portfolio. You’ll own a defined territory, partnering with aesthetic doctors, dentists and nurses to grow revenue, develop KOL relationships and deliver education that builds long-term adoption. Key responsibilities Promote and sell the aesthetics portfolio to qualified HCPs, fully compliant with ABPI and company standards. Build, retain and grow key clinic accounts; identify and convert new opportunities. Create and execute a territory business plan based on data/insight; report monthly on activity, sales and market intel. Engage and nurture KOLs and trainers; support workshops/congresses as needed (some evenings/weekends). Maintain high product knowledge and deliver compelling product/technique presentations. Manage territory budget and company equipment to standard. About you Science graduate (preferred) with ~5+ years’ aesthetics/ Pharmaceutical/ Medical Device experience sales experience and a track record of growth. ABPI qualified / able to undertake and acquire in the first 12 months of employment Consultative, data-driven, great presenter; quick-thinking and solutions-oriented. Strong integrity/ethics; resilient; excellent stakeholder management. Full UK driving licence; competent with CRM and Microsoft 365. Applications: Please apply via this advertisement with an updated version of your CV and a member of our team will be in contact again shortly. Those who do no demonstrate the above requirements will unfortunately not be considered further at this stage Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Regulatory Medical Writing Lead  

    - Surrey
    Overview Job Role: Regulatory Medical Writing Lead Job Type: Full-time... Read More
    Overview Job Role: Regulatory Medical Writing Lead Job Type: Full-time, permanent. Job Location: UK, Remote – Travel 1x a quarter to the office in Surrey. Remuneration: £80,000 – £99,000 plus car allowance and bonus. An opportunity to join a growing specialty pharmaceutical company that focuses on developing innovative treatments for hard-to-treat diseases, with key areas including immuno-oncology, gene therapy, mitochondrial biology, blindness and regeneration, and targeted protein degradation. Acts as a Global Medical Writing Lead, generally in mid- to late-stage development global project teams. The individual provides leadership with respect to all program documents and may act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. The individual independently analyzes proposed program, study, and related documents for their ability to deliver the information required by the target audience (e.g., regulatory authority) with accuracy and consistency. The individual reviews documents within a therapeutic area with respect to consistency with the team/corporate established strategy and document history; ensures a consistent pattern of successful completion of assigned responsibilities within a program resulting in the production of high-quality documents that meet corporate needs and global regulatory requirements; and provides intellectual leadership and contributes document knowledge and expertise to the global project team. Responsibilities: · Acts as a primary lead for all assigned programs (generally mid- to late-stage development). · As a document specialist, provides intellectual leadership and contributes document knowledge and expertise to the global project team. · May act as the departmental expert on IND/IMPD dossier components, briefing documents, and responses to regulatory authorities across programs. · Reviews documents within a therapeutic area with respect to consistency with the team/corporate established strategy and document history, ensuring a consistent pattern of successful completion of assigned responsibilities resulting in the production of high-quality documents that meet corporate needs and global regulatory requirements. · For all documents within a program, independently implements adjustments in specific document content within framework of provided templates in order to fit the needs of specific document/core team requirements. · Participates in standards and processes initiatives/activities and other departmental project activities (up to a total of 15% of time). · May participate in a multidiscipline productivity or process initiative. · Supports Line Management in the improvement of departmental performance and outsourcing alliances through analysis and evaluation of metrics and performance data. Required Qualifications: · BA/BS degree or equivalent, 10+ years relevant experience. Preferred: PhD/Pharm D or MS/MA/MPH with at least 10 years as a writing professional in pharmaceutical industry, with 2-5 years’ experience in managing/supervising activities associated with the creation of regulated documents in the pharmaceutical industry. · Technical expert on all document types produced by medical writing. · Demonstrated and substantial experience in leading/managing the creation of IND/IMPD and NDA/MAA components, briefing documents, responses to regulatory authorities. Preferred experience in preparing for advisory committees. · Strong communication and leadership skills; strategic thinker. Please note this role is a senior role within the business so you MUST have extensive experience in RA medical writing and have excellent communication skills. The role DOES NOT offer job sponsorship so you must hold the full right to work in the UK and be based in the United Kingdom. Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • MSL – Precision Medicine  

    - London
    Overview MSL – 12 Month Contract – £487 per day (Inside IR35) A globa... Read More
    Overview MSL – 12 Month Contract – £487 per day (Inside IR35) A global pharmaceutical organisation specialising in the Haematology, Oncology and Precision Medicine is now in urgent need of an MSL to come on board their field medical teams. The successful MSL will have 2+ years’ experience working within Haematology, Oncology or Precision medicine. Skills and experience required: – · Developing and training MSL’s and various medical professionals globally. · New product launch experience. · Knowledge and experience of working to the ABPI code of practice. · Capturing the discussion process insights. · Experience setting up round tables and advisory boards. · Existing relationships with Haematology or Haem-Oncology KOL’s. · Providing training on the medical communication topics to capture the conversations for global MSL teams. · Setting up MSL’s on study support. · Experience with KOL market mapping. · In-depth knowledge and insight into the NHS landscape. · Broad level of stakeholder management. MSL – 12 Month Contract – £487 per day (Inside IR35) Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Packaging Operator – Projects  

    - Hertford
    Overview The Packaging Operator – Projects – will have the responsibil... Read More
    Overview The Packaging Operator – Projects – will have the responsibility to operate the designated packaging equipment and systems to produce product that meets pre-defined quality attributes and production schedules, at the Production facility in Hatfield and to ensure the efficient operation of all production operations. General Responsibilities (Safety, Quality, Customer, Cost & Innovation) To ensure that operations conducted are performed in accordance with the requirements of the Corporate Standards, Quality System, GMP and GDP Guidelines and Industry Standards. Duties are performed to ensure: A safe working environment is maintained for self and other employees, ensuring all near miss incidents and accidents are reported in accordance with procedures. The Quality of products produced and released is assured through adherence to all procedures. Opportunities to improve operations and reduce cost are identified and progressed through the continuous improvement and demand innovation initiatives. Companies philosophy of hhc is at the forefront of daily activities. All stakeholder and customer expectations are understood and met through communication. Performance is in line with personal and company objectives with demonstrated behaviors and competencies. Working relationships of this position Quality Assurance and Quality Systems to ensure all activities are conducted compliantly and the product meets appropriate quality standards. All Production Operation departments (Warehouse, Manufacturing and Packaging). To ensure compliance to companies policies working relationships are required with HR and Health & Safety departments. Technical Departments, to obtain technical guidance on qualification/validation activities and information of new and existing product/materials. Engineering – to ensure support and maintenance of production equipment and services is available. Job Specific Responsibilities Recording appropriate metrics to monitor adherence to production schedules, equipment utilisation, right first time batch records and adherence to SOP and training schedules. Responsible for compliance to Good Manufacturing Practices in areas of responsibility Responsible for compliance to health and safety procedures in areas of responsibility Support Engineering and Contractor activities To set-up production equipment to ensure correct functionality and calibration compliance. Operate production equipment and automated systems within the validated process Parameters. Conduct manual packaging operations. Carry out in-process tests, yield calculations, product sampling and inspection to ensure all production meets predefined quality attributes Carry out Production Facility Cleaning and Sink and Drain Disinfection. Dismantle, clean and reassemble equipment, ensuring it is well maintained Participate in quality investigations. Identify continuous improvement opportunities that result in cost savings and more efficient and compliant ways of working Responsible for completion of batch documentation Checking the quality standards of packaging components, prior to use on the line Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Electrical and Automation Technician  

    - Hertford
    Overview Our client is looking to appoint an experienced Electrical an... Read More
    Overview Our client is looking to appoint an experienced Electrical and Automation Technician who will report into the Senior Production Engineering Manager, this role is responsible for the reliable and GMP compliant operation of the Production related equipment on Manufacturing and Packaging machinery and supporting systems within our clients facility at Hatfield.  “To ensure that operations carried out within your area of responsibility are carried out in accordance with the requirements of the Quality System, GMP Guidelines and Industry Standards.”  Duties are performed to ensure:  A safe working environment is maintained for self and other employees, ensuring all near muss incidents and accidents are reported in accordance with procedures.  The Quality of products manufactured and released is assured through adherence to all procedures.  Opportunities to improve operations and reduce cost are identified and progressed through the continuous improvement and demand innovation initiatives.  The companies philosophies of hhc is at the forefront of daily activities.  All stakeholder and customer expectations are understood and met through communication.  Performance is in line with personal and Eisai objectives with demonstrated behaviour’s and competencies.   What are we looking for?  Time served apprenticeship or relevant experience  City & Guilds  Btec Level 3  or relevant technical equivalent.  Fault finding skills  Aptitude for neat, clear and concise documentation.  Multi-disciplined.  Good communication and interpersonal skills  Adaptable and flexible to cope with the changing needs of the production.  A determination to understand breakdown/failure root cause and prevent reoccurrence.  Ability to prioritise and plan own work.  Computer literacy.  Good communication and interpersonal skills  Adaptable and flexible to cope with the changing needs of production.  Growth mind set  Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Marketing Manager  

    - London
    Overview Marketing Manager – £38 Per Hour – 24 Months – Surrey A globa... Read More
    Overview Marketing Manager – £38 Per Hour – 24 Months – Surrey A global pharmaceutical client of mine specialising in Oncology, Vaccines and Immunology is now in need of a Marketing Manager to come on board their teams in Surrey. Core skills and experiences required:- · Experience shaping the UK medical strategy. · Experience working to the ABPI code of practice. · Identify and support the customer insights and value proposition plans. · Experience working within an omnichannel environment. · Experience integrating digital channels. · Experience working within the pharmaceutical industry, specifically Vaccines, is a huge bonus. · Vendor management experience; including setting KPIs. Marketing Manager – £34 Per Hour (PAYE) – 24 Months – Surrey Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less
  • Omnichannel Strategist  

    Overview Omnichannel Strategist (Spanish or Italian Speaker) Duration:... Read More
    Overview Omnichannel Strategist (Spanish or Italian Speaker) Duration: 12 months  Location: Uxbridge (Hybrid working 50/50 in office and from home) Pay rate: £49 per hour PAYE Hours: 35 hours per week  Position Summary: The Omnichannel Strategist acts as member of the Worldwide Commercialization Excellence (WCE) for brand teams, pulling in cross-functional resources as needed to ensure successful delivery of omnichannel strategy and campaigns. This role is deployed to brand teams with a focus on HCP, to lead digital and media channel planning in collaboration with our business partners, and leads cross-functional teams (business, matrix, agency partners) to execute and optimize campaigns, tactics, and programs to meet and exceed business strategy and objectives. Purpose & Objective of the Omnichannel Strategist: • Pull through omnichannel brand campaigns, programs, media planning & campaigns and tactics; driving operational effectiveness, business impact and achievement of objectives. • Partner with business and other WCE functions (e.g., Content Delivery and Customer Engagement Platform Team) on development of channel-agnostic engagement strategy followed by more specific digital channel strategy to meet business and customer needs. • Deliver omnichannel insights and recommendations for ongoing optimization of business plans. • Leverage Digital Capabilities and Customer Engagement Excellence principles, standards, and best practices to drive results for the business. Examples include Omnichannel and advanced analytics, content modularisation, CRM, websites, Interactive visual aids (IVAs), email, social media, Remote Engagement and Search Engine Marketing. Other examples to be identified based on business/customer needs and prioritized according to the identified customer experience journeys. • Identify and run experiments with capabilities team to pilot/scale future digital marketing capabilities. • Act as a coach to brand teams to ensure adoption of new ways of working with specific focus on omnichannel strategy Key Responsibilities: • Leads brand omnichannel planning and content strategies across multiple internal business partners including medical, commercial, access, and engaging with multiple customers as prioritized by the brand lead. • Contributes to continuous improvement of engagement, channel, content and analytic planning frameworks and tactical templates to use across cross functional brand teams. • Leads and coordinates regular insights and metrics discussions with business partners in partnership with the AIA team to ensure frequent optimization of the engagement, content and channel plans. • Leads cross-functional matrix teams to enable seamless execution of business strategy and lead execution of digital campaigns/tactics • Collaborates with AIA to ensure KPI identification, measurement plans and optimization of omnichannel campaigns and customer journeys • Coordinates with Customer Engagement Platforms, IT, Digital Production, Content Delivery, and rest of WCE teams on the following activities: • Prioritization of campaigns and tactics • Definition of campaign/tactic success (e.g., development of metrics plan) • Evaluation and optimization of tactics • Driving tactical plan to accomplish KPI and business objectives • Provides omnichannel subject matter expertise into the ongoing evolution of customer engagement model by working with business leads on critical business priorities • Maintains view of the competitive landscape and has a broad perspective across the company and pharma industry to identify and drive best practice around omnichannel expertise • Drives innovation culture and coordinates with business and capability leads to develop innovative digital tactics and apply metrics, analytics, and insights • Identifies long-term process needs of the business partners focused on omnichannel capabilities, developing, and executing a plan to address business requirements • Identify opportunities for synergies and collaboration within and across markets within a therapeutic area • Lead on the relationship with digital agencies/vendors to define project scope, costs, timelines, and deliverables • Partner with content stewards P Production & Content Delivery to provide early insight into cross-market material creation to drive content/asset re-use. • Deliver campaign briefs and other necessary requirements documentation to support the development of programs Monitor, manage and provide regular updates on campaign/project financials • Partner closely with Production and Content Delivery to provide direction, support to project teams, and implement changes when needed to achieve project objectives • Monitor project status and budget and provide regular reporting on progress, challenges, and solutions • Collaborate with other Omnichannel Strategy teams to enable consistency and best practice sharing across the enterprise Required Qualifications & Experience: • Bachelor’s degree required; MBA preferred • 8+ years’ experience in Digital /Omnichannel Marketing leadership, including marketing/customer engagement strategy, brand/business planning, analytics, multi-channel (digital and non-digital) marketing operations and campaign/tactic execution/management. • Additional European languages essential: Italian, Spanish Apply Full name Email address Cover Message (optional) Upload CV Choose File Upload your CV and any other relevant file. Contact via SMS (optional) I would like to be contacted via SMS Privacy Policy I have read and agree to the Clinical Professionals Group Privacy Policy Find our privacy policy here Read Less

Company Detail

  • Is Email Verified
    No
  • Total Employees
  • Established In
  • Current jobs

Google Map

For Jobseekers
For Employers
Contact Us
Astrid-Lindgren-Weg 12 38229 Salzgitter Germany