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  • Sr Manager, Program Resource Management  

    - London
    Job Title: Sr Manager, Program Resource Management Job Location: Londo... Read More
    Job Title: Sr Manager, Program Resource Management Job Location: London, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: HOW MIGHT YOU DEFY IMAGINATION?

    If you feel like you’re part of something bigger, it’s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It’s time for a career you can be proud of. Join us.

    SENIOR MANAGER, PROGRAM RESOURCE MANAGEMENT (PRM)

    LIVE

    What You Will Do

    In this vital role you will be accountable for forecasting, allocating and overseeing resourcing for our global clinical trial delivery team. Using your ability to analyze, interpret and succinctly summarize complex data, you will play a critical role in forecasting departmental resource needs and have a continuous eye on opportunities to streamline & simplify processes.

    Key Responsibilities:

    Resource Forecasting, Planning & Allocation

    Partner with key stakeholders to develop resource forecasts which align with portfolio priorities and budget cycles. Manage workforce forecasting, planning and resource allocations across multiple clinical programs and geographies.Partner with, and oversee our full-service provider (FSPs) to ensure we fulfil program teams’ complex and evolving resourcing needs.Lead the hiring & interview process for new internal clinical delivery staff. Proactively identify, manage & communicate resourcing risks.

    Stakeholder Engagement & Relationship Management

    Serve as a trusted partner to clinical program leaders and their resourcing leads.Facilitate cross-team discussions to resolve conflicting resource priorities and challenges.Build strong, collaborative relationships with FSP partners to foster trust, alignment, and shared goals.Communicate complex resource scenarios clearly and persuasively to senior leadership.

    Data Analysis & Insights

    Analyze large, complex datasets to identify trends, gaps, and opportunities in resource utilization.Leverage AI and predictive analytics to improve forecast precision and agilityDevelop and maintain concise dashboards and reports to support strategic planning (streamlining, simplifying and automating wherever possible).Synthesize complex analysis into concise, actionable insights for senior leadership, framing recommendations within the broader strategic and operational context.

    Process Improvement

    Drive continuous improvement in resource management processes, tools, and systems.Lead and contribute to the development of playbooks, training programs, and knowledge-sharing platforms.Champion best practices in forecasting, scenario planning, and capacity modelling.

    Be part of our team

    You will be joining a dynamic and growing global CPO team, reporting directly to the Director, Clinical Program Resource Management.

    WIN

    What We Expect Of You

    We are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:

    Degree educated and proven experience in life sciences or medically related field, biopharmaceutical clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO companyExpertise in data analysis, interpretation & presentation (ability to extract, analyze, and interpret complex datasets & generate succinct insights).Preferably experience or strong interest in use of AI for analytics.Strategic awareness (understanding of how resourcing contributes to the broader organizational goals). Continuous improvement (background in streamlining and simplifying processes)Experience managing resource allocationsMetrics setting & interpretation (ability to identify the metrics & insights that matter)Experience in line and people managementExperience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)Knowledge of clinical trial processes & operations is prefered

    THRIVE

    What You Can Expect Of Us

    As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

    Vast opportunities to learn and move up and across our global organizationDiverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and actGenerous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

    LOCATION: Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.

    APPLY NOW

    for a career that defies imagination

    In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

    careers.amgen.com

    Equal Opportunity Statement

    Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

    We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Research Associate in Transmission Electron Microscopy  

    - Manchester
    Job Title: Research Associate in Transmission Electron Microscopy Job... Read More
    Job Title: Research Associate in Transmission Electron Microscopy Job Location: Manchester, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Internship Overall Purpose of the Job:

    Transmission electron microscopy is one of the most effective techniques for nanoscale characterisation of 2D materials systems which, combined with advances in fabrication of environmentally sensitive samples, can now be applied to novel 2D materials.

    This post-doctoral research associate position will investigate structure and property variations of novel 2D materials systems with a range of TEM techniques complemented by novel device fabrication methods. This project will utilise advances in fabrication of TEM samples containing chemically sensitive 2D materials to study novel materials systems, heterostructures and devices with unique properties. You will work closely with physicists and material scientists to enable the characterisation and understanding of the phenomena observed within the developed devices.

    Prior experience of STEM characterisation of air and electron beam sensitive 2D materials is essential, including imaging, diffraction and spectroscopy, with experience acquiring 4-dimensional STEM (4DSTEM), differential phase contrast (DPC) and ptychography data being desirable. Direct experience using JEOL ARM300CF, FEI Talos F200A or FEI Titan “ChemiSTEM” (G2 80–200) desirable, as well as experience in TEM/STEM image processing and simulation using open-source Python packages such as atomic simulation environment (ASE) and abTEM. A willingness to occasionally travel (nationally and internationally) to other labs to perform TEM/STEM experiments for a period of days- weeks would also be an advantage.

    What you will get in return:

    Fantastic market leading Pension schemeExcellent employee health and wellbeing services including an Employee Assistance ProgrammeExceptional starting annual leave entitlement, plus bank holidaysAdditional paid closure over the Christmas periodLocal and national discounts at a range of major retailers


    As an equal opportunities employer we support an inclusive working environment and welcome applicants from all sections of the community regardless of age, disability, ethnicity, gender, gender expression, religion or belief, sex, sexual orientation and transgender status. All appointments are made on merit.

    Our University is positive about flexible working – you can find out more here

    Hybrid working arrangements may be considered.

    Please note that we are unable to respond to enquiries, accept CVs or applications from Recruitment Agencies.

    Any CV’s submitted by a recruitment agency will be considered a gift.

    Enquiries about the vacancy, shortlisting and interviews:

    Name: Prof Sarah Haigh

    Email:

    General enquiries:

    Email:

    Technical support:

    https://jobseekersupport.jobtrain.co.uk/support/home

    This vacancy will close for applications at midnight on the closing date.

    Please see the link below for the Further Particulars document which contains the person specification criteria.

    Please be aware that due to the number of applications we are unfortunately not able to provide individual feedback on your application.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Job Title: Senior Scientific and Regulatory Affairs Associate – Contam... Read More
    Job Title: Senior Scientific and Regulatory Affairs Associate – Contaminants & Packaging Job Location: Slough, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Mid-Senior level Job Description:

    Salary from £60,000 plus bonus and car allowance

    Slough - Hybrid working

    We have an opportunity to join Mars as Senior Scientific and Regulatory Affairs Associate – Contaminants & Packaging . As an associate of Scientific & Regulatory Affairs, you'll performs a variety of regulatory activities related to raw materials, finished products, packaging, PREMIA, and regulatory database management to ensure compliance with applicable food and other product-related laws and regulations in accordance with internal processes in the region, related to food contact materials and food chemicals legislation (including but not limited to FCM, REACH, contaminants, pesticides).

    You'll proactively identify potential regulatory problems, and take action to minimize or eliminate such problems and perform other duties to assist in creating a positive scientific and regulatory environment for our products and aligned with our business goals. You'll also work on innovation and external projects to address and resolve regulatory issues that could impact our products across the region (e.g. Codex Alimentarius).

    What are we looking for?

    Education & Professional Qualifications:

    Bachelor’s degree in a technical area, such as nutrition, food science, biology, chemistry or pharmacology or related Preferred: Master’s degree in a technical area, such as nutrition, food science, biology, chemistry or pharmacology, or in food law

    Knowledge/Experience:

    Extensive experience in scientific and/or regulatory compliance/affairs and/or a related technical area with food products or related product categories (such as food supplements, cosmetics, pharmaceuticals and natural health products) with proficiency in food contact material and chemicals law for Europe and UK. Experience working on large-scale regulatory compliance or regulatory affairs projects; a demonstrated track record of working successfully across functions to achieve shared goals; and proven ability to interact cross-functionally at all levels within the organization are required. Experience working with trade associations and government agencies to clarify and resolve regulatory matters is required.

    What will be your key responsibilities?

    As Senior Scientific and Regulatory Affairs – Contaminants & Packaging in Europe & Central Eurasia you will:

    Proactively monitor and provide guidance/recommendations on scientific and regulatory activities in the area of food contact materials and food chemicals legislation for the region. Determine current and expected regulatory status of new and existing materials ; Be responsible for ensuring that standards, systems and processes are in place to ensure newly developed or revised packaging materials meet regulatory requirements so that they can be marketed in the target countries on a timely and cost efficient basis. Develop and execute the external scientific and regulatory influencing strategy related to food contact materials and food chemicals legislation in the region to preserve Mars’ freedom to operate. Represent Mars Wrigley in trade, industry, professional, and scientific associations, driving the agenda in line with business objectives. Develop and manage networks and partnerships to support business strategy and enhance Mars Inc.'s reputation. Works with experts to ensure regulatory compliance and state-of-the-art programs. Lead complex and strategically important SRA projects , with local, regional and sometimes even global scope and impact

    What can you expect from Mars?

    Work with over 140,000 diverse and talented Associates, all guided by the Five Principles. Join a purpose driven company, where we’re striving to build the world we want tomorrow, today. Best-in-class learning and development support from day one, including access to our in-house Mars University. An industry competitive salary and benefits package, including company bonus.

    Mars is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. If you need assistance or an accommodation during the application process because of a disability, it is available upon request. The company is pleased to provide such assistance, and no applicant will be penalized as a result of such a request.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Associate Business Development Director  

    - London
    Job Title: Associate Business Development Director Job Location: Londo... Read More
    Job Title: Associate Business Development Director Job Location: London, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Company Description

    We help brands make BOLD MOVES

    Nowadays, brands want rapid, spectacular growth and they expect media to deliver it.

    Clients used to give us media briefs that said “deliver 80% awareness” or “give me an impactful Christmas campaign.”

    Now we hear

    “Take me from 4th to 1st in my category”

    “Help me grow 10% in a market declining 10%”

    “Make me the most loved brand in my industry”

    These are huge asks of media, that can’t be met through tweaking the media plan of two years ago.

    Decades of advertising research prove that without a big change, large brands stay large and small brands stay small.

    This is why Zenith help brands make BOLD MOVES.

    Bold moves are big, brave changes to media strategy, delivering more impact for brands and more value for consumers.

    Bold moves are backed up with a solid forecast - they are a better path to growth.

    Bold moves build a partnership - we believe in this approach so much we link our growth to your success.

    Bold Moves bring bigger ROI

    This approach works for our clients, our people and consumers - it’s why we are recognised as the UK’s best media agency.

    Our Commitment

    At Zenith UK, we believe that fostering an inclusive culture where all talent can thrive makes our company stronger. It enables a greater idea exchange, which fosters innovation and creativity, and enriches our perspective.We are committed to Publicis Groupe’s wide variety of talent engagement and inclusion programming, and encourage our people to take an active role in continuing to drive positive change within our agency.

    Overview

    Are you ready to play a pivotal role in shaping the future of some of the world’s most dynamic brands? Publicis Media UK is looking for an exceptional Business Development Associate Director to join our award-winning new business team, based at our stunning headquarters in London’s iconic Television Centre.

    As the growth engine behind renowned agencies such as Zenith, Starcom and Spark Foundry, Publicis Media is home to trailblazing thinkers and doers who thrive on winning. From L’Oréal and Sky to Santander and LinkedIn, we don’t just pitch - we deliver industry-leading results.

    You’ll be joining a high performing team, which won Campaign’s Business Development Team of the Year in 2023. We have an exceptional track record for winning business and have had a sustained period of excellence in recent times, including landing the massive L’Oréal & Sky accounts in 2024 and already we have won Monzo, Santander, LinkedIn and retained Asda in 2025.

    The role will sit within a team of new business Associate Directors, Directors, a Group Head and Chief Growth Officer, working across the portfolio of Publicis media brands. This means you will have exposure to and develop skills and knowledge across all areas of media from but not limited to ATL and BTL marketing strategies. This is an exciting and important role within our high-energy and fast-moving division.

    Responsibilities

    In this high-impact role, you’ll lead and support key aspects of the end-to-end pitch process and lead strategic pitches across top-tier brands, driving revenue growth and elevating our agency’s profile.You'll be at the centre of it all - developing pitch strategy, managing RFIs and RFPs, crafting compelling stories, and orchestrating every element from production to performance.This includes market intelligence, analysis, coordination, management and alignment of project pitch deliverables. As part of a growing team, the collaboration, on-boarding and careful management of market resources is crucial.As a mentor, you’ll guide and grow junior talent while ensuring every project hits the mark.This is more than a job - it’s a chance to collaborate with some of the sharpest minds in media, contribute to transformational campaigns, and accelerate your career within one of the most respected marketing collectives globally.

    Qualifications

    Experience in new business or client management with a good grasp and understanding of the marketing/communications/media sphere with an extensive understanding of all aspects of the media processExposure to all areas of media from but not limited to ATL and BTL marketing strategiesA confident storyteller with sharp communication and project management skillsA strategic thinker with deep media industry insightA collaborative spirit who thrives under pressure and leads with purpose

    Publicis Media is built on Trust, Talent, and Transformation - if you’re ready to bring those values to life and fuel the next wave of agency success, we’d love to hear from you.

    Apply now and help us shape the future of media.

    Additional Information

    Zenith UK has fantastic benefits on offer to all of our employees. In addition to the classics, Pension, Life Assurance, Private Medical and Income Protection Plans we also offer;

    WORK YOUR WORLD opportunity to work anywhere in the world, where there is a Publicis office, for up to 6 weeks a year.REFLECTION DAYS - Two additional days of paid leave to step away from your usual day-to-day work and create time to focus on your well-being and self-care.HELP@HAND BENEFITS 24/7 helpline to support you on a personal and professional level. Access to remote GPs, mental health support and CBT. Wellbeing content and lifestyle coaching.FAMILY FRIENDLY POLICIES We provide 26 weeks of full pay for the following family milestones: Maternity. Adoption, Surrogacy and Shared Parental Leave.FLEXIBLE WORKING, BANK HOLIDAY SWAP & BIRTHDAY DAY OFF You are entitled to an additional day off for your birthday, from your first day of employment.GREAT LOCAL DISCOUNTS This includes membership discounts with Soho Friends, local restaurants and retailers in Westfield White City and Television Centre.

    Full details of our benefits will be shared when you join us!

    Publicis Groupe operates a hybrid working pattern with full time employees being office-based three days during the working week.

    We are supportive of all candidates and are committed to providing a fair assessment process. If you have any circumstances (such as neurodiversity, physical or mental impairments or a medical condition) that may affect your assessment, please inform your Talent Acquisition Partner. We will discuss possible adjustments to ensure fairness. Rest assured, disclosing this information will not impact your treatment in our process.

    Please make sure you check out the Publicis Career Page which showcases our Inclusive Benefits and our EAG’s (Employee Action Groups).



    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Senior Medical Writer  

    - Glasgow
    Job Title: Senior Medical Writer Job Location: Glasgow, UK Job Locatio... Read More
    Job Title: Senior Medical Writer Job Location: Glasgow, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Mid-Senior level About Ashfield MedComms

    Uniting the expertise and capabilities of Ashfield and Huntsworth Health, iNIZIO has launched to become THE strategic partner for health and life sciences companies. Unparalleled in scale and expertise, we connect a full suite of Advisory, Medical, Marketing/Communications, Patient and Stakeholder Engagement, and Biotech services to reimagine clients' challenges into opportunities.

    We are a team of 10,000 experts working together in 35 countries to create something extraordinary. We exist to solve health challenges and develop transformational ideas that positively impact human lives. Working at Inizio offers an opportunity to work for a game-changing company built with one goal. That is to redefine health and life sciences by empowering our people to inspire new possibilities that promote health and build brighter futures.

    About The Role

    We're looking for a Senior Medical Writer to work on one our busy accounts, focused predominantly on Publications with some occasional Medical Affairs/Medical Education activities . You will report to a Senior Scientific Team Director and work with the agency's senior leadership team. This role would suit an experienced writer with an interest/experience in, a diverse range of disease areas including Alzheimer's disease, Women's Health, Infectious diseases, Cardiac to name a few, and experience with diagnostics/devices would be useful.

    It will provide a great career development opportunity for you with the support of a very experienced team.

    About you:

    To succeed you will have:

    You will have experience working in a Medical Writing role, within a medical communications agency environment.An academic background in the life sciences.You will have experience writing across a broad range of scientific deliverables e.g. publications, training materials, slide sets, interactive content, conference booths, competitive intelligence, for a variety of medical audiences.

    Benefits include:

    Hybrid or Remote working optionsPrivate HealthcarePension

    In addition to a great benefits package package, we are happy to talk flexible working. We are also known for our friendly and informal working environment with social events across our offices and regular wellbeing programs. We offer excellent opportunities for career and personal development.

    Our Pledge

    We appreciate the importance of having a workforce that reflects the communities in which we operate, and our goal is to create an inclusive environment where diverse employees want to work and where they can flourish.

    Ashfield MedComms is proud to be an equal opportunity employer. Individuals looking for employment at Inizio are considered without regards to age, ancestry, colour, gender, gender identity or expression, genetic information, marital status, medical condition (including pregnancy, childbirth, or related medical conditions), mental or physical disability, national origin, race, religion (including beliefs and practices or the absence thereof), sexual orientation, military or veteran status.

    Ashfield MedComms is part of Inizio Medical. Inizio is a strategic partner for health and life sciences with a full suite of medical, marketing, advisory and engagement services.

    Don't meet every job requirement? That's okay! Our company is dedicated to building a diverse, inclusive, and authentic workplace. If you're excited about this role, but your experience doesn't perfectly fit every qualification, we encourage you to apply anyway. You may be just the right person for this role or others.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Sr. Manager Regulatory Affairs North-West Europe  

    - Haverhill
    Job Title: Sr. Manager Regulatory Affairs North-West Europe Job Locati... Read More
    Job Title: Sr. Manager Regulatory Affairs North-West Europe Job Location: Haverhill CB9, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Director Job Summary

    We offer a position as a Senior Regulatory Manager Taste, subregional lead for EAME Northwest Europe (UK, Ireland, Nordics). This role reports to the Head of EAME Regulatory Affairs Taste and will be located Europe (preferably UK, Germany or the Netherlands). In this role you will be part of the IFF Global Regulatory Affairs team supporting the Taste BU in EAME with a focus on flavorings and seasonings.

    Where You’ll Make a Difference

    Ensure IFF Taste products in the sub-region comply with all relevant regulatory, market, and customer requirements.Lead and develop the UK-based Regulatory Affairs team, fostering growth and collaboration.Streamline and enhance processes for handling technical product documentation requests efficiently and accurately.Provide expert regulatory guidance to local and regional commercial and technical teams.Act as the primary regulatory contact for customers and authorities, offering clear interpretations and defending positions.Monitor and implement changes in food legislation and regulatory requirements across the region.Collaborate with UK industry associations and cross-functional teams to anticipate and respond to legislative changes.Align closely with sub-regional business leads to identify needs, set priorities, and support strategic objectives.Contribute to global and regional projects aimed at advancing regulatory systems, policies, and strategies.

    What Makes You the Right Fit

    University degree in food science, food technology, food chemistry, or a related field.Minimum 10 years of regulatory experience in the flavors or broader food industry.Deep knowledge of EU and UK food and flavor legislation.Proven leadership skills with experience guiding teams in international environments.Strong communication skills in English, both written and verbal.Solution-oriented mindset with excellent problem-solving abilities.Customer-focused approach and a drive for delivering results.Proficiency in Microsoft Office; SAP experience is a plus.Highly organized, detail-oriented, and able to work independently.A collaborative team player with a proactive attitude.

    How Would You Stand Out?

    Experience representing companies in industry associations or regulatory forums.Demonstrated success in implementing regulatory strategies across multiple regions.Ability to influence and build strong relationships with internal and external stakeholders.

    Why Choose Us?

    Be part of a global leader in taste innovation and food science.Work in a dynamic, international environment with passionate professionals.Lead impactful projects that shape regulatory practices and product compliance.Enjoy opportunities for professional growth and leadership development.Collaborate across diverse teams and regions.Make a meaningful contribution to safe, high-quality food products enjoyed worldwide.

    We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability.

    Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Sales Lead (B2B SaaS / CTMS)  

    - London
    Job Title: Sales Lead (B2B SaaS / CTMS) Job Location: London, UK Job L... Read More
    Job Title: Sales Lead (B2B SaaS / CTMS) Job Location: London, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Mid-Senior level About The Role

    We’re hiring an experienced and commercially driven Sales Lead to spearhead the sales function for a high-growth startup revolutionising the clinical trials space with cutting-edge automation technology. This is a unique opportunity to join a mission-led, product-focused company at the forefront of digital transformation in healthcare and life sciences.

    In this role, you will own the full sales cycle, from prospecting to close, while helping shape a scalable and strategic commercial function. You’ll work closely with the C-suite, lead engagement with enterprise clients in the pharma and clinical research space, and play a central role in driving long-term growth.

    Key Responsibilities

    Develop and execute go-to-market strategies focused on pharma, biotech, CROs, and medical research organisations.Manage the full sales cycle, from lead generation to contract negotiation with a focus on high-value enterprise accounts. Deliver product demos and explain complex tech clearly to non-technical stakeholders. Build and manage a healthy pipeline, lead outbound efforts, and report on sales performance to senior leadership. Oversee post-sale success in collaboration with customer success teams to drive retention and expansion. Collaborate cross-functionally with marketing to align campaigns and messaging with pipeline goals. Represent the company at industry events, conferences, and client meetings to build visibility and trust

    Requirements

    10+ years of full-cycle B2B SaaS sales experience in healthcare, life sciences, or clinical trials. Proven track record selling into pharma, CROs, or clinical research environments. Demonstrated success with enterprise deals and working across multiple stakeholder groups (clinical ops, IT, procurement). Strong communication, negotiation, and stakeholder management skills. Comfortable working across global markets (EMEA, North America, Asia). Experience leading sales in a startup or early-stage scale-up environment. Confident working independently while building and evolving sales processes. Technically literate, able to run demos and communicate product value clearly.

    What’s Offered

    A high-impact role in a fast-scaling, mission-driven company. Flexible hybrid working model with access to central offices when needed.Competitive base salary + performance-based bonus scheme with significant earnings potential. Training and support to grow into a senior commercial leadership position. A collaborative, diverse, and positive work culture where your voice matters. Generous holiday allowance, pension scheme, and long-term growth opportunities

    Additional Benefits

    Company pension schemeSick payUK visa sponsorship availableWork-from-home flexibilityMonday to Friday scheduleHybrid remote work based in London N1

    If you are passionate about med tech, eager to make an impact, and ready to grow with an innovative team, we encourage you to apply.

    We are committed to building a diverse, inclusive workplace where every team member is empowered to do their best work. We welcome applications from all perspectives, identities, and backgrounds. Success in this role is shaped by your talent, ambition, and commitment to ethical, patient-focused sales.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Sales Specialist Cell Health and Centrifugation  

    - York
    Job Title: Sales Specialist Cell Health and Centrifugation Job Locatio... Read More
    Job Title: Sales Specialist Cell Health and Centrifugation Job Location: York, UK Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Entry level Bring more to life.

    Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

    At Beckman Coulter Life Sciences, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

    You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

    At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.

    We are partners in time and accelerate answers to critical questions through the power of automation. We develop innovations for scientists by scientists, with many of our 3,300+ global colleagues coming from the laboratory.

    It’s all part of our time-tested approach to bringing meaningful innovations at the speed of life since 1935. And we’re just beginning. Working together, let’s put our time and talents together to advance human health for tomorrow.

    Learn about the Danaher Business System which makes everything possible.

    The Sales Specialist is responsible for Driving sales targets through active engagement with customers, developing and nurturing strong relationships with researchers, scientists and procurement professionals.

    This position reports to the UK Sales Manager for Centrifugation and Cell Health products and is part of the UK CHC Sales team located in Cambridge and the South East and will be a remote role to cover this territory.

    In This Role, You Will Have The Opportunity To

    Developing the sales for cell health & centrifugation products in the respective territory. Maintaining relationships with existing customers and developing new business opportunities. Negotiating pricing strategies to align with customer and revenue targets.Achieving the quarterly and annual revenue targets and providing accurate forecasting and funnel management of future business. Update opportunities as they progress through the funnel on the CRM system.Development and presentation of customer solutions with multiple decision makers, collaborating with cross functional teams to achieve the best solution for the customer. Provide demonstrations and instrument training to end users.

    The Essential Requirements Of The Job Include

    Master’s degree or PhD in biology, biochemistry, or any similar subject area in the scientific/life science field.A minimum of 2 years’ sales experience

    Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role

    Ability to travel –potentially overnight, within territory or EU office locationsMust have a valid driver’s license with an acceptable driving record

    It would be a plus if you also possess previous experience in:

    Cell culture techniquesCentrifugation experience

    Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

    For more information, visit www.danaher.com.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
  • Job Title: Regulatory Project Manager / Business Analyst (12 month FTC... Read More
    Job Title: Regulatory Project Manager / Business Analyst (12 month FTC) Job Location: London, UK Job Location Type: Hybrid Job Contract Type: Full-time Job Seniority Level: Mid-Senior level The Value of Active Minds
    About Jupiter
    Jupiter is one of the UK’s leading investment management companies with just over 500 employees and £44.3 billion worth of assets under management (as at 31st March 2025).
    Jupiter provides investment services to individual and institutional investors through mutual funds (UK unit trusts, Luxembourg SICAVs and Dublin OEICs), separately managed accounts and sub-advised funds. Jupiter has experienced a period of international growth with offices open across EMEA and APAC.
    The majority of our employees are based in our London office located just minutes from Victoria station which provides stair-free access from both the Underground’s Victoria line and National Rail platforms, as well as limited road crossings to the Jupiter office. Our London office was designed to encourage employees to live active, healthy lives with floor-to-ceiling windows that allow for greater natural light and the benefit of a private balcony, table tennis room, cycle storage and on-site shower and locker facilities. The short distance to Green Park and St James' Park also provides employees with a natural space to relax during their lunch break and a healthy alternative to office-based meetings.
    We offer our UK employees a 3:2 hybrid working arrangement where Tuesdays, Thursdays and a third day of your choice are worked from the office. The other two days may be worked from home. This facilitates collaboration and allows employees to maximise productivity whilst maintaining a healthy work/life balance.
    Background
    This is an exciting time to join the Change team at Jupiter. The Strategy & Transformation Department has recently been created to support Jupiter in delivering its wider business strategy and transformational initiatives. The Change Team, (which was previously part of Technology), is part of this function, and sits alongside the Corporate Development function, reporting to the Chief Strategy and Transformation Officer. The Change team will deliver an ambitious and transformational book of work to achieve Jupiter’s strategic goals.
    The growth of the Change team, and the creation of this PM/BA role, reflects the increased size and scale of Jupiter’s change appetite as we embark on a multi-year transformational change agenda that will deliver strategic initiatives across the entire firm. This role offers high exposure and requires close collaboration with senior stakeholders across the business. It will require building strong collaborative and cross-functional relationships across many areas of the firm. The role holder will undertake their responsibilities in a way that aligns with our cultural pillars - our clients come first, our value is in our people, we succeed together, we strive to challenge ourselves.
    Key Responsibilities
    Project Manage all aspects of the end-to-end regulatory and compliance aligned project delivery
    Coordinate regulation requirement gathering and propose a clear definition of the scope and business value of your project. Take responsibility to ensure all interested parties have a transparent and consistent view of what your project will deliver.Identify logical grouping, sequencing, and delivery approach of key milestones. Propose a delivery framework and resource profile to support this.Quantify the business benefit/rationale of your project and design a metric(s) to report the delivery value of the project throughout its duration.As part of your project design, identify operational BAU impacts of your project, and propose solutions on how these will be managed post-delivery.Maintain up to date transparent tracking of your project, incl risk/issue information, that can be extracted on an ad-hoc basis and will provide a real time snapshot of your project status.Design roadmaps and implementation plans including organisational cross dependencies. Tailoring the roadmap so it can be used for both detailed working groups, and senior management audiences.Manage/chair/lead the Steering/Working/Project groups/committees and/or projects, including assisting with the production of related project documentation.Be ready to quickly provide succinct options and recommendations to senior stakeholders when delivery risks arise.Identify and implement potential solutions, systems, tools, processes, and frameworks to improve the ongoing optimisation of the Change Team’s Operating model.Robustly manage project financials including initial estimate, budgets, and forecasts.Be aware of the industry and regulatory landscape. Research and provide insights as to how similar projects/problems are being tackled in the market. Consider and demonstrate these insights when designing your project approach and timelines.Continually improve how we work, consider the lessons of the last project, and how we can adapt the way we deliver change to maximise outcomes for our clients and stakeholders.
    Proactively manage strong working relationships to enable nimble delivery of projects
    Build strong partnerships between business functions and the Change team, across both London based colleagues, as well as overseas.Manage external suppliers/vendors who are engaged on your project, manage the work that they deliver in line with the statement of work.Partner closely with the Technical Delivery Team to identify the technical requirements of your project, understand their development and test timelines, and manage accordingly within your project plan.Work closely with your Change team colleagues, share best practices and be aware of challenges across the wider portfolio of change. Show an interest in the other Project Mangers challenges and capacity issues, working as a team to collectively support.Identify all relevant stakeholders within the remit of your project, design an appropriate comms and engagement strategy appreciating the needs and detail will differ across the group.Form close collaboration with your project sponsor, proposing an efficient governance model that will provide the right level of oversight whilst being conscious of stakeholder’s time and availability.Build close relationships with the SMEs and working group members who will support the delivery of your project. Build trust and understand the wider and competing work priorities of this group to foresee delivery risks and plan accordingly.Take a pragmatic risk-based approach to the project artefacts, whilst meeting Jupiter’s project delivery framework standards, further assess what items will require ratification and decision. Design the most effective way of proposing recommendations and documenting outcomes for future reference or audit.
    Desired Skills / Experience
    At least 10+ years' experience in a combination of PM and BA roles in financial servicesFamiliarity with the Asset Management industry, client trends, competitor landscape, regulatory and operational frameworksExperience in delivering large scale regulatory programs of work.Experience in project initiation including business case definition, set up, structure and right fit governance.Experience in developing complex cross functional road maps and implementation plans, with the ability to identify, track and manage dependencies from multiple sources.Ability to multi-task and deliver more than one single regulatory initiative at a time.Previous Business Analysis experience to support regulatory and compliance related requirement gathering and post implementation review, and gathering MI to support benefit realisationExperience of working to inflexible and regulatory timeframes.Fluency in core technology and data concepts and underpinnings, such as data structure and data quality.Strong knowledge of regulatory landscape.Previous delivery experience in UCITS regs is a plus.Knowledge of programming languages is a plus.A commitment to become cognizant of Jupiter’s technical architecture and corporate structure is required.Strong understanding of equity, fixed income, and alternative investments. Experience of a consultancy background, or a demonstrable ability to show that you can quickly move from project to project and “hit the ground running”, is a plus.
    Personal Skills and Qualities:
    Excellent verbal and written communication skills with an aptitude for presenting – tailoring the message based on nature of client and size of audience. Results-orientated – able to self-manage to deliver tasks with high attention to detail.Partnership focused – able to understand and connect with various stakeholders across the Company whilst also providing constructive challenges.Leadership - can galvanize a team, create momentum, and maintain energy. Resilient – able to cope in a fast moving and challenging environment. Organised – capable of working to deadlines and multi-tasking. Persuasive – demonstrating credibility through knowledge.Perceptive - able to understand perspectives/requirements of investors, sales and clients.Team player – helping to build out knowledge, share experience and dependencies with the wider business and Change team Technology proficient – experienced in using various systems, applications, software.
    Additional Role Details
    This role is subject to the Conduct Rules set by the FCA.
    Don’t meet every requirement? At Jupiter we are dedicated to building a diverse and inclusive workplace, so if you are interested in this role, but don’t think your experience aligns perfectly with every listed requirement in the job description, we would encourage you to apply. You may be the right person for this role.

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less
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    Join us and build a €1B+ company with us!

    This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Read Less

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