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We are looking for an enthusiastic Teacher of Biology to join our dynamic and successful department. All pupils study biology, chemistry and physics as separate subjects in Year 9. They choose at least two sciences for GCSE, although most take three. Around 200 pupils undertake Sixth Form study in science and around 50 each year go on to read a science-related subject at university. \n The depth of ex... \n \n \n \n \n \n ZIPC1_UKTJ

Job ID: 31166545Company: Abbott LaboratoriesLocation: Maidenhead, State Not Indicated, United KingdomEmployment type: full timeCategory: Regulatory AffairsIndustry: HealthcarePosted: 2026-11-05 Primary Objective of Position Candidates should take the time to read all the elements of this job advert carefully Please make your application promptly. • Leads Regulatory Affairs strategy and activities across assigned EU/EFTA, UK, Region East, and Region Türkiye markets, ensuring regulatory compliance, market access, lifecycle management, and effective management of regulatory risk., • Leads assessment and implementation of evolving regulatory requirements, engaging with regulatory authorities and trade associations to determine compliance strategies and communicate business impact., • Provides regulatory leadership and guidance to commercial and cross-functional teams to support compliant business activities, market access, and lifecycle management., • Acts as Regulatory Affairs lead and designated backup across assigned regional markets, ensuring continuity of regulatory support and compliance oversight., • Develops and executes regulatory strategies for registrations, promotional review, performance studies, customer and tender support, and regulatory governance activities, including DOA requirements., • Provides leadership and direction to regulatory colleagues across assigned markets, driving collaboration, capability development, accountability, and consistent execution of regulatory activities. Major Accountabilities • Ensures that all activities are performed in compliance with quality system requirements., • Reviews regulations from the assigned area countries and elevates according to CDx specific elevation process; assesses for impact and initiates and supports implementation action plans as needed; provides input into draft regulations to trade associations or competent authorities, • Responsible for following of the implementation of regulatory compliance as required by international & local regulations and Abbott policies and procedures., • Performs product notifications/registrations in the assigned countries, following country-specific requirements, processes and timelines, • Acts as a primary contact for country regulatory Authorities, • Cooperates with key trade Associations, • Supervises process for responding to customer and tender requests; provides responses to requests as needed, • Acts as an SME for EMEA Promotional material review process, • Performs approval of labelling and Ad Promo material in own native language, • Responsible for obtaining and maintenance of regulatory approval of all Core Diagnostics and Molecular Diagnostics products intended for distribution in Region East assigned countries., • Executes tasks required for regulatory compliance in areas of product notification/ registration, responding to customer and tender requests, promotional material approval in the assigned countries, performance evaluation and DOA distribution, • Ensures DOA distribution requirements are met in assigned countries, • Ensures performance study requirements are met guidance, notifications, submissions, follow-up with authorities and ethic committees. xrnqpay, • Supporting communication among divisions, dealers and health authorities to be able to get product approvals without any damage to given timelines, • Ensures that knowledge and experience acquired during their professional life is transferred to other team members, • Perform /act as backup for Registration / notification process in the assigned countries, • Perform above mentioned activities for Abbott divisions specified in service agreements, • Represents RA in audits. Education and Background • Scientific background (Degree in Medicine, Biology, Chemistry or Similar, • Proven experience in IVD or similar industry, • Significant experience working in an international work environment or on international projects, • Project management and negotiation skills, • Fluent in English (written and spoken), • Strong communication skills, • Ability to work independently, with attention to detail, • Knowledge of PC- and internet-based applications, • Leadership Skills

Director, Senior Global Regulatory Lead (Sr. GRL)Global Regulatory Strategy (GRS)Location: King of Prussia, PA | Waltham, MA | Maidenhead, UK | Zurich, SwitzerlandWork Arrangement: Hybrid – 3 days onsite per weekAbout CSLCSL’s R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a strong focus on collaboration, we’re building a future-ready organization that thrives in dynamic biotech ecosystems. Join CSL and become part of an agile team committed to developing therapies that make a meaningful difference for patients around the world.The OpportunityThe Director, Senior Global Regulatory Lead (Sr. GRL) is a key member of CSL’s Global Regulatory Strategy (GRS) organization and serves as the global regulatory leader for assigned products within the respective therapeutic area.In this highly visible, strategic role, you will develop and lead innovative, science-driven global regulatory strategies across the product lifecycle, from early development through registration and post-marketing activities. You will serve as the primary Global Regulatory Affairs (GRA) representative on Product Strategy Teams (PSTs) and other cross-functional development teams, ensuring regulatory strategies are integrated into product development decisions and aligned with broader business objectives.As a trusted regulatory partner, you will build and maintain productive relationships with global health authorities, particularly the FDA and EMA, while guiding regulatory teams through complex development and approval pathways. You will influence strategic decisions, anticipate regulatory challenges, and identify opportunities to accelerate the delivery of innovative therapies to patients.Depending on the role, you may also lead and develop Regional Regulatory Leads, fostering a collaborative, accountable, and high-performing global team.Key ResponsibilitiesDevelop Global Regulatory Strategy: Establish and lead integrated, science-based global regulatory strategies for assigned products, supporting development, registration, and post-marketing lifecycle activities while balancing innovation, patient needs, and business priorities.Lead Cross-Functional Regulatory Partnership: Serve as the primary GRA representative on Product Strategy Teams and partner with Clinical Development, Safety, Commercial, Research, and other key stakeholders to ensure regulatory considerations are incorporated into product strategy and decision-making.Drive Health Authority Engagement: Lead strategic relationships and interactions with key health authorities, including the FDA and EMA, and collaborate with regional regulatory partners to support successful regulatory outcomes across global markets.Provide Regulatory Leadership and Oversight: Lead the Global Regulatory Affairs Strategy Team (GRAST) for assigned products, establishing priorities, coordinating deliverables, assigning responsibilities, and ensuring alignment across global regulatory functions.Influence Product Development Decisions: Serve as the primary GRA reviewer and, where appropriate, approver of key development deliverables, including protocols, Target Product Profiles (TPPs), and other strategic documents. Provide regulatory guidance to senior leadership and cross-functional teams.Lead Strategic Regulatory Deliverables: Oversee the development of key regulatory documents and initiatives, including Core Briefing Books, Orphan Drug Designations, Pediatric Study Plans, and Global Regulatory Strategy Outlines.Drive Regulatory Intelligence and Innovation: Leverage competitive regulatory intelligence, emerging technologies, AI-enabled insights, business analytics, and specialized regulatory expertise to inform strategy, assess opportunities, and proactively address potential challenges.Promote Global Regulatory Alignment: Build strong relationships across Global Regulatory Strategy, including regional regulatory teams and Regulatory CMC, to promote consistency, knowledge sharing, and a unified global regulatory approach.Lead and Develop Talent (where applicable): Coach and develop Regional Regulatory Leads, establish clear performance expectations, foster accountability, and support succession planning and career growth.Champion CSL Leadership Capabilities: Demonstrate CSL's leadership capabilities by building partnerships, thinking strategically, driving outcomes, embracing agility, inspiring innovation, and cultivating talent.Qualifications & ExperienceEducationBachelor's degree in Pharmacy, Biology, Chemistry, Pharmacology, Clinical Medicine, or a related life science discipline required.Advanced degree (MS, PhD, MD, DVM) or MBA preferred.ExperienceMinimum of 10 years of experience in the biotechnology or pharmaceutical industry, including at least 8 years in Regulatory Affairs.At least 5 years of experience supporting pharmaceutical or biological product development.Demonstrated experience leading teams, preferably with 5 years of direct or matrix leadership experience, including setting strategic direction, driving accountability, and developing talent.Strong knowledge of pharmaceutical and biological product development and regulatory requirements across multiple major regions, including the US, EU, and/or Japan.Demonstrated experience working directly with at least one major health authority, such as the FDA or EMA.Experience navigating complex, global, matrixed organizations and influencing cross-functional stakeholders.Strong clinical development or medical device expertise is highly desirable.Leadership & CompetenciesThe successful candidate will bring:Strong strategic thinking and the ability to translate complex regulatory considerations into actionable development strategies.Excellent communication, influencing, and relationship-building skills, including the ability to engage effectively with senior leadership and health authorities.Sound judgment and confidence in making complex regulatory decisions and taking calculated risks.The ability to lead through influence, foster collaboration, and drive accountability across geographically dispersed teams.A patient-focused mindset and passion for advancing innovative therapies through successful development and approval.The expected base salary range for this position at hiring is $242,000 - $270,000. Please note this salary range reflects the minimum and maximum base pay that CSL expects to pay for this position at the time of this posting in MA. Individual base salary for a successful candidate is determined by qualifications, skill level, experience, competencies and other relevant factors. In addition to base salary, total compensation for this role may also include incentive compensation and equity.#LI-HYBRIDAbout CSL BehringCSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at .Our BenefitsFor more information on CSL benefits visit How CSL Supports Your Well-being | CSL.You Belong at CSLAt CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belongingEqual Opportunity EmployerCSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit .SummaryLocation: Americas, US-PA, King of Prussia, CSL Behring; EMEA, CH, Kanton Zurich, Opfikon, CSL Vifor; EMEA, GB, Berkshire, Maidenhead, CSL Behring; Americas, US-MA, Waltham, CSL BehringType: Full time

Career Category Clinical Job Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Let’s do this. Let’s change the world. In this vital role you will generate evidence to meet Health Technology Assessment (HTA) requirements, while ensuring that the analyses performed meet required standards and are robust and valid. • Achieve results through detailed goal setting, accountability measures, effective partnerships, collaboration with other groups and a dedication to serving customers, both inside and outside of CfDA, • Represent CfDA at multi-disciplinary teams, advocating for robust and appropriate statistical strategies, • Contribute to all aspects of evidence generation to meet HTA needs, including Systematic Literature Reviews (SLRs), Evidence Synthesis Feasibility Assessments (ESFA), analysis methodology, and technical report production, • Complete statistical analysis of evidence generation projects, • Support departmental activities including methodology research, analysis toolkit development, and creation and roll-out of training materials, • Stay up to date with HTA policies and requirements, and statistical advances in the HTA setting You would be joining the Design & Innovation group within the Center for Design and Analysis (CfDA). 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: • Educated to PhD level in Statistics/Biostatistics, • Statistical experience in the pharmaceutical industry or medical research, • Knowledge of R and other statistical software (e.g., SAS), • Excellent communication skills and ability to work optimally within teams while also possessing the capacity to autonomously manage tasks and projects, • Preferably, experience of working on HTA evidence generation projects, from strategy planning through to analysis, reporting and submission As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer. We make all employment decisions without regard to race, color, religion, sex or any other characteristic protected by applicable law. We provide reasonable accommodations to applicants and employees with disabilities, consistent with legal requirements. Please contact us to request accommodation. Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. For more information, visit www.amgen.com and follow us on www.twitter.com/amgen #J-18808-Ljbffr

At Bristol Myers Squibb, our employees often ask, "Who are you working for?"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Are you a hands-on data scientist with a passion for turning complex, multi-modal data into actionable insights that shape clinical decisions? Bristol Myers Squibb is seeking a Senior Manager, Data Science to join our Drug Development Data Science & Advanced Analytics (DSAA) team. • Develop and apply novel computational methods for patient segmentation, biomarker discovery, and hypothesis generation from multimodal clinical and omics datasets, in partnership with Translational, Clinical, and Statistical Scientists, • Execute data science analyses on datasets from BMS clinical trials and real-world data cohorts, spanning genomics, proteomics, imaging, flow cytometry, and other high-dimensional biomarker data types, • Develop innovative approaches to integrating, mining, and visualising diverse, high-dimensional, and disparate datasets generated across early-to-late phase drug development, • Formulate, implement, test, and validate predictive models and build efficient, automated processes for delivering modelling results at scale, • Apply modern machine learning capabilities - including AI/ML, deep learning, NLP, causal ML, and explainable AI - across multiple data modalities and clinical development contexts, • Apply statistically rigorous approaches to clinical trial data, including survival analysis, longitudinal/mixed-effects modelling, and appropriate handling of missing data and censoring, • Contribute to the scientific and statistical strategy of drug development programs, including the development of predictive biomarkers, novel trial designs, and precision medicine approaches, • Build and maintain well-structured, reproducible, version-controlled analytical pipelines and codebases using Python, R, SQL, and cloud platforms, • Develop and apply data quality frameworks to assess and ensure fitness-for-purpose of diverse data sources for specific analytical questions, • Implement strong model evaluation practices including cross-validation strategies, calibration assessment, and transparent reporting of model performance and limitations, • Build scalable, automated processes for delivering analytical results across multiple programs and data types, • Partner with lead and protocol statisticians in contributing to statistical analysis plans (SAPs) for exploratory data science analyses supporting drug development programs, • Collaborate with cross-functional teams including clinicians, translational medicine scientists, biostatisticians, data engineers, and IT/engineering professionals, • Contribute to team excellence through code reviews, technical mentorship, and raising the overall engineering and methodological standards of the team, • Communicate analytical strategies and results clearly and effectively to both technical and non-technical stakeholders, with strong data presentation and visualisation skills, • Manage and coordinate deliverables across concurrent, fast-paced projects within tight timelines, • PhD in a relevant quantitative field (e.g., Computational Biology, Biostatistics, Statistics, Biomedical Engineering, or Computer Science) with 1+ years of academic/industry experience; or a Master's Degree in a relevant quantitative field with 3+ years of industry experience, • Strong experience in data science and statistical analysis using clinical trial or electronic health records data, particularly in a pharma R&D context, • Experience developing and validating statistical and machine learning models on high-dimensional data for time-to-event, longitudinal, and multivariate outcomes, • Experience in the application of AI/ML and proficiency in Python, R, SQL , and cloud platforms (e.g., AWS, Azure, Databricks), • Familiarity with clinical trial design, drug development processes, and the role of biomarkers in regulatory and clinical decision-making, • A perspective on leveraging innovati #J-18808-Ljbffr

OverviewThe Associate Director, Biostatistics is responsible for statistical activities in support of clinical trials, including contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and reviewing and interpreting the analysis of clinical trial data.This is a hybrid position, based two days a week onsite at our offices in Maidenhead.Key ResponsibilitiesRepresents biostatistics at cross-functional team meetings to drive clinical development of drug candidate and provides input on clinical development plans.Collaborates with Clinical Development, Regulatory and Clinical Operations Expertise Areas to design clinical trials.Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.Contributes to or prepares statistical analysis plans.Collaborates with Data Management, Clinical Development and Clinical Operations on design of eCRFs.Provides statistical guidance on conduct of ongoing trials.Collaborates with Statistical Programmers on summary and analysis of trial data.Writes ADS and ad hoc analysis specifications.Contributes to clinical study reports and other regulatory documents e.g. Apply now, read the job details by scrolling down Double check you have the necessary skills before sending an application. DSURs, Briefing Documents, etc.Represents Alnylam in meetings with regulators, Key Opinion Leaders, partners, and other stakeholdersContributes to scientific articles, summarizing data collected in Alnylam trials.Participates in other activities and meetings to support Biostatistics and the Development Team as needed.Consults with Research & Preclinical colleagues on statistical questions in their work.Manages CRO statistical and programming support.QualificationsPh.D. in Biostatistics or Statistics or Equivalent with at least 7 years pharmaceutical biostatistics experience; or MS with at least 10 years relevant experience.Excellent written and oral communication and presentation skills.Experience programming in SAS.Interest in and basic understanding of biology and biological processes, including RNAi.Desired ExperienceExperience in clinical development through Phase 3 (NDA submission).Experience as lead statistician for a compoundUnderstanding of ICH GCP as well as general knowledge of industry practices and standards.Proficiency in R programming language and other statistical software, including EAST.Experience with CDISC, including SDTM, ADaM, CDASH.Experience in representing sponsors in meetings with interaction with US FDA and international regulatory authorities.Experience designing and conducting adaptive trials.#LI-LR1 #LI-HYBRIDAbout Alnylam: Alnylam Pharmaceuticals (Nasdaq: ALNY) has led the translation of RNA interference (RNAi) into a whole new class of innovative medicines with the potential to transform the lives of people afflicted with rare and more prevalent diseases. Based on Nobel Prize-winning science, RNAi therapeutics represent a powerful, clinically validated approach to treating diseases at their genetic source by “interfering” with mRNA that cause or contribute to disease. Since our founding in 2002, Alnylam has led the RNAi Revolution and continues to turn scientific possibility into reality.Our culture: Our people-first culture is guided by our core values: fiercely innovative, open culture, purposeful urgency, passion for excellence, and commitment to people, and these values influence how we work and the business decisions we make. Thanks to feedback from our employees over the years, we’ve been fortunate to be named a top employer around the world. Alnylam is extremely proud to have been recognized as one of Science Magazine’s Top Biopharma Employers, one of America's Most Responsible Companies for 2024 by Newsweek, a Fast Company Best Workplace for Innovators, and a Great Place to Work in Canada, France, Italy, Spain, Switzerland, and UK – among others.At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. We are dedicated to building an environment where employees can feel that they belong, can bring their authentic selves to work, and achieve to their full potential. By empowering employees to embrace their unique differences at work, our business grows stronger with advanced and original thinking, allowing us to bring groundbreaking medicines to patients. xrnqpay Before applying, please review Alnylam's ⁠Candidate Privacy Notice regarding how Alnylam handles Personal Data you provide with your application for employment.

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FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.Whether you’re a private tutor or prefer online sessions, we provide the platform to connect with students across the UK.No previous tutoring experience required.Flexible hours and remote teaching opt

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

FindTutors is looking for passionate Biology tutors to join our growing online teaching community.

We are looking for an enthusiastic Teacher of Biology to join our dynamic and successful department. All pupils study biology, chemistry and physics as separate subjects in Year 9.

This tenure-track Group Leader post sits in the Cell Biology Division of the Laboratory of Molecular Biology, part of the Medical Research Council. Develop and lead a research programme on fundamental cell or tissue biology, or on methods for studying them. Studying fundamental processes in molecula

EMBL-EBI, part of the European Molecular Biology Laboratory, is a worldwide leader in the storage, analysis and dissemination of large biological datasets.

The Laboratory of Molecular Biology (LMB), part of the Medical Research Council, invites applications for a tenure-track Group Leader to build and run an independent research programme in cell biology.

Ideally 3+ years in fermentation process and extraction techniques and/or vector construction/molecular biology. Familiarity with modern lab equipment and digital tools relevant to synthetic biology and fermentation; English is the working language; additional languages are a plus. Synthetic Biology

European Molecular Biology Laboratory (EMBL-EBI) is launching a Digital Transformation Specialist role to drive EMBL-wide change programmes, with an initial focus on HR and expanding to Finance and Procurement.

A leading biotechnology recruitment firm seeks a Synthetic Biology/Fermentation R&D Scientist for an innovative company near Shanghai, China.

A leading life sciences organisation in Cambridge is looking to appoint an experienced Head of Computational Biology to lead and develop its computational biology capability. A PhD or equivalent experience in computational biology, bioinformatics, genomics, systems biology or a related discipline. T

Durham University invites applications for a Laboratory Technician to support Dr Jeongmin Choi's laboratory.The post is full-time, fixed-term for 2 years with an option to extend for 1 year.The role supports a friendly and vibrant team in a brand-new laboratory that prioritises wellbeing and a posit

Develop the intent, implementation and impact of the Biology curriculum, ensuring it is ambitious, coherent and engaging, while enabling students to appreciate the relevance and application of Biology in the wider world. We are looking to appoint a talented, dynamic and passionate Subject Leader of

You hold a PhD (or equivalent experience) in machine learning, computational biology, or structural biology, with a proven track record of applying machine learning to real-world protein structure or drug discovery challenges. Lead the technical strategy for machine learning applications in structur

Seeking an hourly paid lecturer for GCSE and Access Biology evening classes.

Seeking a Head of Biology with KS5 experience for a secondary school in Kingston. Responsibilities include teaching KS5 Biology and guiding the curriculum alongside the Director of Science.