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At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. Within Pharma Research & Early Development (pRED), our Ophthalmology teams are redefining how precision medicine can transform the detection and treatment of complex retinal diseases. This is a rare opportunity to build a new function from the ground up — establishing an Ophthalmology Precision Medicine group at our Welwyn site that brings together biomarker science, advanced imaging, clinical expertise, and artificial intelligence. You will have the platform, pipeline, and resources to shape something truly new in one of the most dynamic areas of ophthalmic research. • Build a new Ophthalmology Precision Medicine function from the ground up — defining the vision, structure, and scientific direction for a group that integrates biomarkers, advanced imaging, clinical science, and AI across the pRED Ophthalmology portfolio, • Lead a cross-functional expert team spanning translational medicine, imaging, clinical development, data science, and biomarker disciplines — ensuring precision medicine is at the heart of our Ophthalmology strategy, • Bridge laboratory science and clinical practice by steering the generation of robust fluid- and imaging biomarker strategies that enable project and disease area decisions, • Advance innovation in imaging science by directing cutting-edge ophthalmic imaging approaches including OCT, OCT-A, and FA to inform future clinical practice and therapeutic development, • Enable translational insights through AI and data by integrating preclinical and clinical datasets using classical and next-generation analytical approaches, • Influence portfolio strategy across multiple retinal diseases including neovascular AMD, diabetic macular edema, geographic atrophy, and intermediate AMD — driving the direction and future of clinical development and research, • Represent Roche externally through strong partnerships with scientific experts, investigators, and the broader ophthalmology community — remaining at the forefront of innovation, • You are a board‑certified ophthalmologist (MD or MD/PhD) with deep expertise in ophthalmology, translational medicine, or biomedical sciences, • You are a recognised expert in the retina space, with a strong scientific publication record and standing as a key opinion leader in your field, • You have deep knowledge of ophthalmic imaging technologies (OCT, OCT‑A, FA) and experience with imaging analysis or Reading Centre environments, • You are experienced in integrating preclinical and clinical data to support proof of biology, efficacy, and safety strategies, with some exposure to clinical trials, • You are a collaborative scientific leader who thrives in matrix environments, energised by innovation and the opportunity to build something new, • Experience applying AI or machine learning to ophthalmic imaging analysis or clinical data interpretation, • Prior experience in pharmaceutical drug development programmes for retinal diseases, • Flexible working arrangements may be available for exceptional candidates who wish to maintain some clinical activity alongside this role If building a world‑class precision medicine function and shaping the future of ophthalmic therapy development is the kind of challenge that excites you — apply now and help us bring transformative medicines to patients faster. Who we are A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life‑changing healthcare solutions that make a global impact. Let’s build a healthier future, together. The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work. #J-18808-Ljbffr

Genentech is seeking a qualified Global Head of Biostatistics based in Welwyn, UK. The role involves providing leadership for Biostatistics teams, ensuring strategic objectives are met across therapeutic areas. The ideal candidate will possess over 15 years of experience in the pharmaceutical industry and a PhD in a related field. This position includes strategic decision-making and partnerships with key stakeholders. A relocation assistance is available, aligning with Genentech's commitment to developing top talent. #J-18808-Ljbffr

AECOM is seeking a Regional Director - Fire Engineering. This is a consultancy-based role requiring demonstrable experience across sectors and client-focused delivery in fire engineering. • Lead and manage the team in terms of workload management, project delivery and performance., • Oversee the successful delivery of large, complex projects, ensuring they meet regulatory requirements and client expectations., • Collaborate with multi-discipline teams and national leadership to ensure projects are completed on time, within budget and to a high standard of quality., • Lead the Performance & Review process for the team by setting and monitoring SMART goals for team members., • Carry out staff appraisals and ensure direct reports perform similarly for their reports in line with the Performance & Review process., • Participate in developing professional development plans for staff and encourage expansion of expertise across sectors., • Assist in training and mentoring to meet technical development goals in line with PDPs., • Provide specialized technical input to studies and design projects across the portfolio., • Support and mentor less experienced staff on the path to Chartership., • Provide estimates for fire engineering budgets and schedules on large, complex projects., • Lead project delivery on mid to large size projects nationally and internationally., • Lead strategic direction as an AECOM Approved Lead Verifier and act as project approver., • Lead technical client relationships and play a major role in attracting new work and clients., • Ensure work quality and timely delivery within agreed periods and budgets., • Ensure implementation of AECOM Health & Safety policies in the workplace and during off-site activities., • Maintain good client working relationships., • Promote the Fire Engineering business and contribute to growth by attracting internal and external clients., • Support the national team in achieving KPIs., • Develop and support recruitment strategies and business plans for national fire teams., • Assist in implementing marketing strategies focused on collaborative client communication., • Contribute to the Fire Team Business Plan and implement it across the team. Perks at AECOM include core and personalized benefits, career development opportunities, flexible hybrid working, technical practice networks, AECOM University, and volunteering days. Requirements: • Experience in working on fire engineering projects in the UK., • Extensive experience in a large, multi-disciplinary environment., • Comprehensive knowledge of UK guidance and standards (e.g., ADB, BS 9991/9999/9992, HTM 05-02, BB100)., • Proficiency with fire engineering tools such as FDS, SFE, and evacuation modelling software., • Membership in relevant professional institutions (e.g., MIFireE) and/or certifications (e.g., NFPA CFPE). Preferred requirements: • UK or other nationalities; security clearance., • Chartered Engineer (CEng) with the Institution of Fire Engineering., • Extensive knowledge of FDS, evacuation modelling, and structural fire safety engineering., • MSc or PhD in a fire-related field., • International experience with standards such as IBC, SFPE and NFPA. #BESPECIALISMS #BEFIRE At AECOM, we are committed to a secure and trustworthy recruitment process. All new hires must attend Day 1 onboarding at an AECOM office location as a condition of employment. All information will be kept confidential according to EEO guidelines. We are an Equal Opportunity Employer and a Disability Confident Employer. ReasonableAccommodationsUKI@aecom.com may be used to request accommodations during the interview process. AECOM is a global infrastructure consulting firm delivering services from advisory through design and construction management. We serve public and private sector clients across transportation, buildings, water, energy and the environment with a commitment to equity, diversity and inclusion and ESG priorities. AECOM is a Fortune 500 firm with substantial revenue and global reach. #J-18808-Ljbffr

Medical Director - Neurodegenerative Diseases (Alzheimer's Disease) Contract | Outside IR35 Hybrid - 2 days per week onsite (Welwyn Garden City area) An innovative global biopharmaceutical organisation is seeking an experienced Medical Director - Neurodegenerative Diseases to support late-stage clinical development programmes in CNS, with a primary focus on Alzheimer's disease. This role offers the opportunity to contribute to pivotal Phase III programmes aimed at addressing significant unmet medical needs in neurodegeneration. You will play a central role in translating cutting‑edge science into high‑impact clinical strategies, helping to bring potentially transformative therapies to patients. This is a high‑visibility, cross‑functional leadership position within a global matrix environment. • Support the design and execution of global clinical development strategies across all phases, with strong emphasis on Phase III programmes, • Provide medical monitoring for ongoing interventional clinical trials, • Contribute to protocol development, study design, and data interpretation, • Partner closely with cross‑functional teams including Clinical Operations, Safety, Biostatistics, Regulatory Affairs, Clinical Pharmacology, Biomarkers, and Research, • Support preparation for regulatory interactions and health authority engagements, • Participate in advisory boards and engage with external investigators and key opinion leaders, • Translate clinical data into strategic development decisions, • MD or MD/PhD (medical degree required), • Minimum 5 years' experience in longitudinal clinical research, including hands‑on clinical trial experience (industry or academic setting), • Strong experience supporting or leading Phase II‑III development programmes, with particular focus on Phase III, • Experience in medical monitoring of interventional studies, • Proven ability to work effectively within global, cross‑functional matrix teams, • Experience interfacing with regulatory authorities and external stakeholders, • Excellent written and verbal scientific communication skills, • Direct experience in neurodegenerative diseases, particularly Alzheimer's disease, • Experience designing late‑stage CNS development strategies, • Prior experience within a global pharmaceutical or biotechnology organisation, • Involvement in regulatory submissions, • Peer‑reviewed publications in neurology or neurodegeneration, • Brings strong late‑stage CNS clinical development expertise, • Is confident in medical monitoring and protocol design, • Operates effectively in a complex, global matrix structure, • Is comfortable engaging with regulators and external experts, • Combines scientific rigour with strategic thinking, • Contract position, • Outside IR35, • Hybrid working: 2 days per week onsite in the Welwyn Garden City area If you are passionate about advancing innovation in neurodegenerative disease and want to contribute to high‑impact late‑stage programmes, we encourage you to apply. #J-18808-Ljbffr

As the Global Head of Biostatistics, you will provide strategic leadership and oversight across all Therapeutic Area (TA)-aligned Biostatistics teams, ensuring a cohesive and high-performing Biostatistics function that drives excellence in service of our strategy through study design, data analysis, and insights generation. You will report to the Global Head, PD Data Sciences & Analytics (PD-DSA), and you will be responsible for shaping the Biostatistics strategy across all therapeutic areas in alignment with broader PD-DSA and company objectives, as well as your organization’s overall performance. Your role will be instrumental in advancing innovative statistical methodologies, fostering collaboration across internal and external stakeholders, and ensuring the highest scientific rigor in all statistical activities. You will lead a global, high-performing organization of approximately 100‑125 Biostatistics professionals focused on late-stage development. Your direct reports will be a team of five therapeutic area–aligned Biostatistics Leaders. Sitting on the PD-DSA leadership team, you will collaborate with senior leaders in PD-DSA and beyond to influence and contribute to the overall strategy and success of late‑stage development programs at Roche. • Develop and set a clear PD-DSA strategy and goals that align with Roche’s broader objectives, ensuring that you integrate Roche’s One Pharma strategy, PD goals, and R&D Excellence methods into the strategic direction., • Embed and drive the adoption of PD-DSA’s strategic imperatives of Data, Digital/AI, and Design (the 3Ds) across your teams’ workflows, taking ownership of this mindset shift to ensure a seamless integration of these principles into daily operations., • Act as a role model for your teams by delivering excellence in all aspects of your work (what you do, how you do it, and the impact you have), fostering a culture of learning, growth, and continuous improvement that empowers team members to reach their potential., • Define and create clear accountability across each function in your organization and beyond, ensuring that you work in lock‑step with your colleagues and partners to maintain alignment and drive cross‑functional collaboration., • Provide strategic leadership and oversight across all five Therapeutic Area‑aligned Biostatistics leaders and their teams, ensuring a consistent and high‑quality approach to Biostatistics across all therapeutic areas., • Develop and implement a comprehensive Biostatistics strategy that aligns with Roche’s research and development objectives., • Ensure that biostatistical considerations are integrated early in study designs and development programs, aligning with regulatory and scientific best practices., • Partner closely with senior leadership across PD-DSA, clinical development, regulatory affairs, and data science teams to shape the future of statistical contributions within Roche., • Represent Biostatistics as a strategic function, influencing high‑level decision‑making and driving cross‑functional collaboration to optimize study designs and data strategies., • Evaluate challenges as they arise and develop innovative solutions for teams to execute., • Act as the primary liaison between the Biostatistics function and key stakeholders across Clinical, Regulatory, and Data Science teams to drive alignment and shape outcomes for shared objectives; connect key stakeholders with therapeutic area Biostatistics Leaders as nuanced questions arise., • Ensure seamless collaboration between Biostatistics and external partners, including regulatory agencies, academic institutions, and industry consortia., • Represent Roche in industry forums, regulatory discussions, and cross‑industry collaborations to influence and stay ahead of emerging biostatistics trends., • Align closely with the PD‑DSA‑led Innovation Council and broader AI strategy to ensure Biostatistics contributes meaningfully to the company’s digital and AI transformation initiatives., • Ensure the highest scientific rigor and adherence to regulatory standards in all statistical methodologies and study designs across therapeutic areas., • Champion the adoption of AI, digital, and advanced statistical methodologies to enhance study designs and improve efficiency in data analyses., • Oversee the prioritization and implementation of modern digital and AI capabilities in study design and statistical approaches., • Maintain and enforce compliance with industry regulations, GCP, and biostatistical best practices across all programs., • Lead, inspire, and develop a high‑performing global team of biostatistics leaders, ensuring their continued professional growth and ability to drive strategic impact., • Establish a strong culture of accountability, innovation, and continuous learning within the Biostatistics function., • Define clear performance metrics and success criteria for the Biostatistics function, ensuring alignment with organizational goals., • Partner with P&C and leadership to attract, retain, and develop top biostatistical talent to support long‑term organizational success., • PhD, or other advanced degree in Statistics, Biostatistics, or Mathematics., • More than 15 years experience (significant experience working at a senior level) in the pharmaceutical/biotech industry with an emphasis in molecule and molecule‑enabling strategy; ability to consult and understand medical issues., • In‑depth knowledge of Good Clinical Practice (GCP), international and in‑country regulations, guidelines and their application, and all other applicable compliance standards related to data and statistical sciences and industry conventions., • Thorough understanding of the end‑to‑end drug development lifecycle, particularly on elements involving data and statistical sciences, advanced analytics methods and data visualization tools and techniques., • Experience and understanding of the new trends with all relevant data types (e.g., high‑dimensional data) and analytics., • Track record of establishing successful internal and external partnerships with relevant partner organizations and ability to act as an ambassador for Roche., • Willingness to adopt new technologies and methodologies, deep interest in AI and digital advancements., • Influential and confident communicator., • Strong English language skills., • International travel as required – estimated at 20%. Relocation assistance is being offered for this position. • South San Francisco, CA, • Boston, MA, • Basel, Switzerland, • Welwyn, UK, • Mississauga, Canada The expected salary range for this position based on the primary location of South San Francisco, CA is $338,240 - $443,940. Actual pay will be determined based on experience, qualifications, geographic location, and other job‑related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company’s policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. #J-18808-Ljbffr

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Multi Drop Delivery Driver Class 2.We require a reliable, hard working person to deliver soft drinks, crisps and confectionery products to our regular weekly customers.We deliver to trade/business customers within the hospitality sector.This role is working Monday to Friday starting at 6am with flex

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