Pop Science

Do you have a strong foundation in medical statistics ideally in registries, experience in statistical coding, and a passion for using data to drive research in cardiovascular health? We're supporting one of our clients, a renowned healthcare institute, in their search for a Statistician. As part of a small, dynamic and growing team, you will have the opportunity to work with other statisticians and medical writers, as well as directly with leading clinicians and multi-disciplinary team members. You will play a crucial role in supporting research that is aimed at improving cardiovascular health outcomes. Working closely with cross-functional teams you will analyse real-world evidence and apply statistical methodologies to derive meaningful insights. Note this is a permanent full-time position working directly for our client who are based in West London. You will need to work from their offices on three days a week. Key Responsibilities: Collaborate on current clinical research projects, help with the design of new clinical studies and publish research in clinical scientific journals Apply statistical techniques to analyse real-world evidence related to thrombosis and cardiovascular health Assist in the design and execution of experiments or studies related to cardiovascular health outcomes Be part of the clinical research fellowship program, designed to educate clinicians in research methodology Develop and maintain statistical models to support research initiatives Clean, prepare, and validate data for statistical analysis Utilise statistical software, with a preference for SAS, to conduct data analysis and create visualisations Prepare clear and concise reports and presentations to communicate findings to non-technical stakeholders Stay up-to-date with industry trends and advancements in statistical methodologies Support acquisition and implementation of new information sources, data collection strategies, and analytics Help staff with data manipulation and analytic methods to improve analytic deliverables when required. Skills and Experience Required: A master's degree in an area pertinent to the subject area, e.g. statistics, epidemiology, predictive modelling techniques, etc. Candidates with a Bachelor's degree with extensive working experience will also be considered Strong knowledge of statistical concepts and methodologies Proficiency in statistical coding, with a preference for SAS. Experience with R, Python, or other statistical software will also be considered Good oral and written communication skills Proven publication track-record in one or more of the following areas: statistics, machine learning, computational optimisation, open source software, predictive analytics, clinical research Ability to apply data mining techniques and statistical modelling to large amounts of population health data to discover optimal treatment and utilization patterns that can lead to improved health outcomes. If this opportunity suits your skills and experience, and you would like to find out more, please apply today!

We are looking for a leading SVP of Sales and business development with expertise in CNS, Medical Imaging and Data Analytics to join our innovating client. Our client has firmly established itself as a trusted partner to the global life sciences industry, supporting the development of new therapies for neurological conditions such as Alzheimer's, Parkinson's, Huntington's Disease and Multiple Sclerosis. To help us deliver our medical image analysis solutions to large clinical trials we are hiring an experienced SVP, Business Development in a full-time capacity. Please note that we have one position open to either a US or UK/Europe based candidates. Purpose of the Role: Oversight of development and execution of the company commercial strategy in support of the company 5-year growth plan and annual operating budget. To provide sales leadership and line management of the Business Development team to develop and convert the opportunities pipeline to ensure achievement of the company's commercial goals and financial targets. Includes direct business development management responsibility for a number of defined key accounts. Management reporting. Submit monthly reporting to CEO and update the Senior Leadership Team on commercial initiatives in monthly business review meetings. Includes monthly New Bookings Contract (NBC) forecasting to support quarterly revenue forecast updates and other commercial KPI's such as opportunities pipeline development. Also, as required, present commercial updates to the Board. Qualifications and skills required for the role: Senior commercial line manager with excellent sales and line management experience. Able to set clear direction of expectations and BD team alignment on "what good looks like". Excellent communication and interpersonal skills, with a track record of ability to work with senior peers and through others to deliver cross functional company goals. Established neuro and / or imaging professional network with a track record of growth within the CRO clinical trials market. Minimum of a life science degree qualified and experienced in technical consultative scientific sales process. Significant plus if within the neuroimaging trials marketplace. Financial acumen demonstrated by experience or formal training/qualifications. Track record of prospecting and developing contract opportunities across North American, European and Asian CRO landscape would be a significant plus. Must have already built a strong professional network with senior clinical and procurement professionals within the global Pharma and Biotech industry. Demonstrated skills, knowledge and experience in the design and execution of account plans. Be able to demonstrate a deep understanding of what effective, multi-level key account management looks like. Location & travel Home based. Europe or US Management meetings at the company's London HQ as required. International travel to industry conferences and client meetings, particularly in Europe and N. America. Anticipated to be up to 30% international travel We've got a great Lead/Principal Data Scientist role for biomarkers in our rapidly growing and market leading precision medicine and ML AI client. You will lead high-impact research projects at the interface of machine learning, computational biology, bioinformatics and drug discovery & devel Are you passionate about clinical development? We have an exciting Inside Sales Director for our client who provides unrivalled biostatistics and operations research knowledge to their customers in the life sciences industries in the form of both software and service Are you passionate about clinical development? We have an exciting Inside Sales Director for our client who provides unrivalled biostatistics and operations research knowledge to their customers in the life sciences industries in the form of both software and service + Statistics

Are you passionate about AI / ML predictive models in diseases and high quality data for studies in anti-infectives and vaccines? Increase your chances of an interview by reading the following overview of this role before making an application. We are delighted to be working with an exciting London based company looking for a data supply manager. Objective of the role: The Data supply manager will be the owner of key data supply acquisition to support critical business initiatives. The role holder will work on priorities defined by the business and customer facing squads to continue to develop first party data assets. You will identify opportunities to materially increase coverage of key data points through identification of new sources, including public contribution, commissioning of primary market research, and working with sales to include terms in customer contracts to support data supply. The role holder will be reporting to the Director, Data partnerships & strategy. Key Responsibilities: Responsible for increasing data coverage of vaccine uptake by manufacturer and by country from a variety of sources, including commissioned primary research as well as private and public sources. Identify opportunities to source vaccine commercial contracts which highlight government/manufacturing process. Work with sales team to identify contractual approaches to securing relevant primary data. Identify further additional data points as required by our products. Assess incremental value by source, and cost/benefit analysis to inform further investment. Work with the business on operationalising these data collection processes. Skills and Qualifications: Knowledge of vaccine development processes and market. Established expertise in identifying and curating vaccine Life Science data, ideally in the field of vaccines. Innovative, creative and persistence approach to solving data problems. Experience in working across cross functional teams to achieve objectives. Awareness of data concepts and their relevance to data supply. Detailed orientated in assessing data value. Experience in working in a market facing capacity. Life Science degree, masters or PhD.

*We've got a great role for a Regulatory Affairs Manager to work on a market leading technology supporting patient centred clinical trials. While others rely on aggregated data which blocks subject re-engagement, my client can rapidly reach back to contact patients for clinical studies, engage in data collection from home, and to collect biomarker and genomics samples.* *Key Skills* *Will have 3-5 years experience and a deep understanding of the evolving Governance and Regulatory landscape for digital health technologies, the life science sector and challenges facing health tech SMEs and their quest for globalisation. In addition, knowledge and experience working with healthcare organisations, contract research organisations and pharma to understand their needs. This role will report directly to the VP of Product and Compliance. * *Key Responsibilities * * *Develop and implement a quality and regulatory strategy for the UK, EU and North America.* * *Keep abreast of regulatory developments within or outside of the company as well as evolving best practices in governance.* * *Ensure that effective systems and controls are in place to meet regulatory, legislative and corporate governance requirements* * *Work collaboratively with the leadership team to address any governance or regulatory deficiencies or risks* * *Lead the development, management and review of SOPs and other Quality Management Documents* * *Support the team in embedding good regulatory and governance processes into practice and manage any company training programs required * * *As required, monitor any new standards, risks or changes in legislation that may impact the company.* * *Work with the sales and business development teams to manage new and existing Sponsor and Healthcare Organization relationships - specifically understanding their governance and regulatory requirements, ensuring their needs are met.* * *Act as point person on any external audits including those with Sponsors, Healthcare Organizations and any regulatory agencies* * *Act as lead in the development of compliance requirements to support HIPAA, ISO 27001, SOC 2 and GDPR certifications* * *Select and manage any tools required to support regulatory compliance* *Core Skills * * *Self-motivated and ability to prioritize busy workload in a fast-paced environment * * *Have an intimate understanding of the regulatory and governance challenges faced health tech SMEs* * *Have sound knowledge of the relevant regulations, standards and requirements (e.g. MDR, ISO 27001/9001/13485, HIPAA, GDPR, Cyber essentials plus, DSP toolkit)* * *Have practical experience managing and maintaining ISO compliant products with strong operational governance processes.* * *Have knowledge and experience with global (country/local) regulatory and legal requirements related* * *Be passionate about our mission to support better execution of clinical trials * *Company Culture * *No matter what an organisation is trying to achieve, success or failure is inextricably linked to the people within it. For a young company, there is no redundancy so this relationship is turned up to eleven. * *We punch well above our weight due to the quality of the team we have built, and their dedication to our shared vision. Recognising this dedication we have a fantastic benefits package and accompanying culture. This includes: * * *A meaningful share options package so that you own a part of the company and get rewarded for all of your hard work * * *28 days holiday (including bank holidays) * * *Remote first work environment * * *Job Type: Full-time Competitive Salary* *#MDR #ISO 27001 #HIPAA #pharmajobs #remoteworking*

We've got a role for an experienced Software Quality Assurance specialist with experience in writing test cases in Appium. Our client is an exciting and innovating growing healthtech company. They operate at the interface of biotech, pharma and digital technology industries, using the concept of convergence to create new closed-loop models of care pathways, integrating feedback to optimise outcomes for patients and health systems. We have an opportunity for a Quality Assurance Engineer to join our expanding team. You will play a key role in developing mobile applications to deliver innovative treatments to patients in the form of medical device software. Your focus will be on designing and implementing manual test cases, complemented by automated tests written in Appium to provide a robust automated test suite. You'll also play a central role in debugging activities, defining corrective actions, as well as reviewing system requirements and helping CLM track quality assurance metrics. Ultimately, we need someone who can participate in all stages of our software development process to help us meet our quality goals and build great products. *Responsibilities and Duties* * Understand product requirements and goals, and translate these into detailed, comprehensive and well-structured test plans and test cases. * Write automated test cases in our custom automation framework based around Appium. * Review requirements, specifications and technical design documents to provide timely and meaningful feedback. * Estimate, prioritize, plan and coordinate testing activities. * Identify, record, and track defects, and ensure thorough regression testing takes place when defects are resolved. * Provide input into requirements gathering and risk analysis processes based on product observations and experience. * Track quality assurance metrics, such as defect densities and open defect counts. *Required Qualifications, Knowledge, Training and Experience* * Significant relevant experience as a Quality Assurance Engineer * BSc or equivalent experience in either a Software Engineering, Computer Science, Medical, or other Healthcare related discipline * MSc level qualification preferred * Experience with standard software productivity tools for planning, documentation, and defect tracking preferred, preferably the Atlassian suite (Jira, Confluence) * Experience with a test management and documentation tool, preferably TestRail. * Ability to develop automated tests cases using Appium * Knowledge and experience testing medical device products under ISO62304 / ISO13485 would be a strong differentiator but is not an essential requirement *Key Personal Characteristics* * Effective interpersonal skills and strong communication talent in order to establish sound relationships with colleagues, key partners and clients * Methodical, with the ability to follow procedures accurately * Organisational skills with the ability to prioritise your own workload * Ability to work under pressure and meet deadlines whilst showing attention to detail * Flexibility, with an enthusiastic and confident approach; a willing member of the team * Dedicated to driving business growth, developing others and self * Enjoys setting exemplary standards This is a full-time role. The team are currently all working from home, however you will be expected to work ideally 3 days per week in a London office location once office working resumes. They offer competitive salaries, company pension and death in service benefit. Our client believe strongly that the team is fundamental to both their personal fulfilment and the company's success. From the start, they have embedded an extremely supportive and cohesive ethos into the company. #tester #softwaretester #appium #medicaldevice #medtech #softwareQA #londontestergathering