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An exciting opportunity has arisen for a Quality Assurance (QA) Officer within the QA Department of Smithers Environmental Risk Sciences (ERS) Ltd, based in Harrogate. The Business performs Environmental and Consumer Safety Contract Research and Regulatory Services for the Crop Protection, Pharmaceutical, Industrial Chemical, and the Consumer Product industries. Smithers ERS has performed standard guideline and higher-tiered Environmental studies for over 45 years and conducts studies to satisfy all Regulatory requirements globally. Key offerings include Environmental Fate, Plant and Animal Metabolism, Aquatic and Terrestrial Ecotoxicology, Honeybee and Pollinator testing, Avian Toxicology, Residue, Analytical, and Product Chemistry, and Regulatory Risk assessment. The Business is privately owned, highly entrepreneurial, relationship-driven and would provide a solid platform to further develop your skills and knowledge. Reporting directly to the Director of Quality Assurance, you will work within our busy Quality Assurance (QA) Team to assure Management that the Company’s scientific research activities comply with Good Laboratory Practice (GLP) regulations (MHRA/OECD). The role is full time at 37 hours per week, fully onsite. • Conduct audits of protocols, data, reports, and processes to verify compliance with GLP, internal SOPs, and applicable regulatory guidelines (e.g. MHRA, OECD)., • Accurately and concisely report audit findings to laboratory personnel and management., • Participate in facility, process, and computer system audits to ensure ongoing compliance and identify areas for improvement., • Maintain QA audit schedules, training records, and controlled documents., • Communicate effectively (verbal and written) when interacting with staff members., • Assist in preparing for and supporting sponsor, and regulatory inspections., • Provide training to operations staff in the areas of quality systems procedures (SOPs) and regulatory compliance., • Additional duties as assigned. The successful candidate will possess the following skills and experience: • Bachelor of Science/Arts (BSc/BA) degree; degree in a science field is preferred., • Strong Quality Assurance experience, preferably in GLP or a proven work history in a regulatory environment working to GLP., • Comprehensive knowledge of, and the ability to interpret, MHRA/OECD GLP Regulations, • Good writing, numeracy and computer skills., • Excellent communication skills, with the ability to work well with people at all levels of the Organisation., • Possess excellent organisational skills., • The ability to identify opportunities for improvement and drive to successful implementation., • Experience of CSV auditing and the ability to train others, in a range of QA related activities, would also be advantageous. We offer opportunities to work in a fast-paced team alongside bright, interesting colleagues while building a flexible and rewarding career. • private healthcare, • employer matched pension contributions, • free mortgage advice service, • 25 days annual leave plus Bank Holidays, • eyecare vouchers, • Ride2Work scheme, • and more. There is no better time to join us! #LI-CJ1 #Smithers #QualityAssurance #QualityOfficer #EnvironmentalScienceJobs #J-18808-Ljbffr

Experienced Vet? Enjoy the freedom of sole charge, with the support of a wider clinical network. Looking for a Veterinary Surgeon role that gives you clinical autonomy, genuine flexibility and the opportunity to take ownership of your caseload, while still having a supportive team around you? Welcome to Scarborough Vets for Pets. We’re looking for an experienced RCVS-registered Veterinary Surgeon with 3+ years’ experience who is confident working independently and enjoys the variety and responsibility that comes with sole charge. This is a fantastic opportunity for a vet who wants to have a real influence on how they work, with the freedom to make clinical decisions and develop their own areas of interest, while having access to support when needed. This is an exciting opportunity to build your career while enjoying all that Scarborough has to offer. With award-winning beaches, easy access to the North York Moors National Park, affordable housing, excellent schools and a vibrant local culture, Scarborough provides an exceptional quality of life alongside a rewarding professional opportunity. • No OOH or Sundays – enjoy protected evenings and weekends, • 1 in 3 Saturday mornings on a fair and manageable rota, • Clinical freedom with the opportunity to influence how the practice develops, • A supportive and collaborative team, with occasional sole charge, • Flexibility to shape your role around your clinical interests, • Full support for certificate progression and further development Based inside Pets at Home in central Scarborough, our practice provides a modern, bright and welcoming environment for our colleagues, clients and patients. You’ll have access to excellent facilities and equipment, including: • IDEXX laboratory, • Dental X-ray, • Fully equipped theatre, • Provet PMS, • Regular support from visiting specialists You’ll be joining a friendly, community-focused practice where you’ll have the independence to work confidently as a sole-charge vet, alongside access to support and expertise whenever you need it. We’d love to hear from you if you: • Are an RCVS-registered Veterinary Surgeon, • Have 3+ years’ experience, • Are confident working in a sole-charge environment, • Are comfortable managing routine consultations, surgery and your own caseloadHave excellent communication and interpersonal skills, • Are confident making independent clinical decisions, • Are passionate about outstanding patient and client care, • Enjoy having autonomy and contributing to the development of a practice, • Are interested in certificate progression, with full support available, • Up to £85,000 FTE DOE, • £5,000 welcome bonus or relocation support, • Generous CPD allowance and certificate funding, • Paid RCVS, VDS and BVA memberships, • 5.6 weeks’ holiday, increasing to 6.6 weeks after two years’ service, • Contributory pension scheme, • 20% colleague discount across Pets at Home, Vets for Pets and Groom Room, • Wellbeing support and pastoral care, • Genuine career progression opportunities within a leading UK veterinary group Scarborough offers the perfect blend of career and lifestyle, with: • Beautiful sandy beaches on your doorstep, • A fantastic selection of cafés, restaurants and local nightlife, • Easy access to the North York Moors, • Excellent transport links to York and beyond Whether your ambitions are clinical, surgical or leadership-focused, we’ll support you to build a role that works for you. We’re also happy to consider part-time or surgically focused applications. Imagine finishing your shift and heading straight to the beach – with a career that works for you, not the other way around. If you’d like any further information about this vacancy, the practice or Vets for Pets, please contact our Talent Acquisition Team via for an informal and confidential conversation. YO12 4DD We’re also keen to speak with vets, RVNs, and experienced practice managers who are ready to take the next step into ownership. • Immediate brand recognition, • Access to over 8 million Pets Club customers, • A salary from day one We take our inspiration from pets in embracing people from all walks of life, and we value, respect and celebrate difference. We encourage our people to be their best selves so that we can create a better world for Pets, our Planet, and People. Our ambition is to reflect the diversity of the communities we operate in, and we are intentional in addressing and removing barriers to create opportunities for the exceptional talent and potential in our communities. Even if your skills and experience don’t perfectly align, if you think you can make a unique contribution through your values and behaviours, we want to hear from you! #J-18808-Ljbffr

Labcorp Harrogate, England, United Kingdom Get ready to redefine what’s possible and discover your extraordinary potential. Here at Labcorp Drug Development, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career. The Company - LabCorp Drug Development As one of the world's largest and most comprehensive drug development services companies, LabCorp Drug Development has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today. The Position - 1 year contract This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. This position is remotely based. Do you excel at coordinating events and information into a complex timeline? If you have a background in science or experience in project management, then joining our study team as a Temporary Regional Study Coordinator (RSC), an associate project manager role, could be the gateway to unleash your extraordinary potential with a career in project management. Our RSCs manage local laboratory operations and serve as the bridge between our internal departments and various clinical studies. To be successful, RSCs must manage many competing interests, and communicate and articulate critical information to each department and amongst the project management team. About The Job You’ll join our Global Project Management Department, a team of exceptional people who are unified by an energizing purpose to transform healthcare and improve lives around the globe. Clinical studies are developed and managed collaboratively by a study team, and the RSC manages the day-to-day activities of a clinical trial at a regional level. RSCs manage multiple studies and the responsibilities for each include: • Collaborate with the Global Study Manager for all local study related aspects. Specifically, study set up and closure; ordering of study start up supplies, answering CRA questions regarding country specific regulations, etc., • Act as regional liaison between Global Study Manager and various CLS departments involved in the study., • Act as a regional liaison between assigned client representatives (e.g., CRAs or Site Monitors) and Covance CLS internal departments and teams., • Monitor, track and provide resolution to all local study issues; especially logistic issues and/or delays in receipt of study supplies, while keeping the Global Study Manager in the communication loop., • Clean the laboratory database; determine why a lab sample placed on hold is not being analyzed, resolve the issue., • Deliver outstanding customer service and timely responsiveness to ensure client satisfaction, which requires a clear understanding of study design and major budget drivers., • Work in a matrix environment where some task assignments are channeled to RSCs while others are delegated to other functional groups. Your Skills • Excellent communication and organization skills, • Demonstrated time management skills, • Dedicated to teamwork, • Ability to plan and prioritize, • Thrive in a fast-paced environment, • Fluency in English at a work-proficiency level Requirements • A bachelor’s degree and customer service experience. A university degree in science is preferred, but not required if you have demonstrated project management experience., • First experience in client facing role and/or project management, • Good understanding of Central Lab Services or clinical research/studies, • To help you reach your Labcorp Potential, we provide a robust training program followed by structured mentorship, as well as continued support via independent and digital learning programs. You will have opportunities for advancement and be a part of a community of hard-working people who push new boundaries together. Thrive personally and professionally at Labcorp Drug Development Working at Labcorp Drug Development, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s lives. Labcorp Drug Development offers great benefits, global experience and the opportunity to work independently within a team-oriented environment. Get to know Labcorp Drug Development At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our diagnostics and drug development capabilities, we provide insights and accelerate innovations that empower patients and providers and help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 75,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Labcorp Is Proud To Be An Equal Opportunity Employer Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination. Qualified applicants will receive consideration without regard to race, religion, color, national origin, sex, family or parental status, marital status, sexual orientation, gender identity, age, veteran status, disability, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We encourage all to apply If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. • Entry level, • Full-time, • Research, Analyst, and Information Technology, • Hospitals and Health Care Referrals increase your chances of interviewing at Labcorp by 2x Northallerton, England, United Kingdom — 3 days ago #J-18808-Ljbffr

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is seeking to hire a Program Manager to join our Early Phase Development Solutions (EPDS) department supporting pre-clinical studies. This role offers hybrid or on site working aligned with either our Huntingdon or Harrogate site. The Program Manager acts as a single point of contact for our clients and provides them with a Program Management service assisting in the design, conduct and coordination of multidisciplinary, integrated programs, involving pre-clinical and clinical studies and/or the management of client portfolios, at all Labcorp locations, including other Labcorp Business Units and third-party vendors. A Program Manager will have significant interactions with clients by email, phone, and face to face and will provide a program management service for clients placing low - mid complexity packages (portfolios) of work. The Program Manager will work independently on programs or client portfolios but may be assigned to scoped work with either an Alliance Manager, Director Drug Development & Regulatory Strategy (DD&RS) or a CPC Regulatory Program Director. The Program Manager may also monitor the scientific and regulatory acceptability of the program and completion within agreed scope, with support of scientific staff. Work Schedule: 37h/week, Monday-Friday 8:45am-5pm • Ensure appropriate commercial documents are in place prior to studies, including CDA's, contracts, and any quality/technical documents with the client and any third party vendors, • Liaise with the relevant commercial organization team members to ensure post-award handoff, including sharing all documents, timelines and program scope, • Review and evaluate awarded scope, identify any operational challenges, and suggest solutions, • Prepare and host kick off meeting with internal study teams and client representatives, • Set up and lead program debrief after all studies within the development program are completed, • Responsible for the management and tracking of individual project resources needed throughout the development program. Contribute to contingency planning for key resources and activities, • Manage third party vendors as necessary, including overseeing milestones and billing/invoicing, • Engage with key SMEs to provide expert knowledge of Labcorp service lines and capabilities, including sites where work is performed, • Prepare and maintain the appropriate tools, such as Gantt, study trackers, financial trackers, communication plan, risk log, action trackers, etc. for each program, ensure that they are maintained and the program teams, including the client, are provided with regular updates, • Independently provide a program management service for low - mid complexity drug development programs to the client including coordination of internal and external teams across multiple Labcorp business units globally; may provide program management service for higher complexity programs with support from a Director Drug Development & Regulatory Strategy DD&RS or a CPC (Crop Protection and Chemical) Regulatory Program Director, • Lead the core program team, including Study Directors, Principal Investigators, Project Managers from individual business units, and third party vendors for low - mid complexity programs; assist in leading the core team for higher complexity programs with support from a DD&RS or a CPC Regulatory Program Director, • BSc in the Life Sciences field or equivalent industry experience, • Demonstrable client facing experience within pre-clinical field; CRO experience advantageous, • Strong oral and written communication skills, • Ability to work to deadlines, prioritize tasks and manage multiple changing priorities, • Excellent customer service skills with a strong focus on client needs, • Strong planning and organizational skills, • Computer proficiency with good working knowledge of a range of I.T packages, • Ability to work with financial information, • Capable of working autonomously but also in a team environment acting as a mentor where appropriate Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. #J-18808-Ljbffr

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is seeking a remote Study Design Lead to join our Central Labs Services team in the United Kingdom. • Accurately interpret and translate sponsor protocol requirements into the protocol specific database to generate a Statement of Work for the CLS project., • Leverage technical, therapeutic area, client, and company specific process knowledge to provide a comprehensive and complete database design., • Interact with external clients regularly through all duties and responsibilities., • Liaise with internal departments to understand full company capabilities and assess feasibility of requests to meet client needs related to study design., • Act as a consultant to advise on study design choices and work with the Global Study Manager (GSM) to highlight risks and budget impacts associated with study design. Expand consultancy capability at study program levels., • Display strong interpersonal and communication skills that will build strong internal and external relationships to ensure high quality study design., • Coordinate internal processes and communications related to study design (including but not limited to internal feasibility requests, material transfer agreements and supply forecasting) and ensure the eventual follow up is integrated into the database and global monitoring plan. Perform quality self-review., • Ensure that all customer requirements with relation to study design are documented and acted upon., • Act efficiently in an environment with dynamic timelines and priorities., • Display appropriate self-organization and ability to manage conflicting priorities., • Participate in functional meetings (e.g. Continuous Learning Forums (CLFs)) and provide input, keeping processes up to date., • Comply with our internal Central Lab Global Project Management strategy., • Manage a portfolio of global and local studies with varying complexities., • Support a culture of continuous improvement, quality, and productivity., • Bachelor’s degree in a life science, • 6 or more years of experience working in the clinical research industry or within a lab environment, • Master degree in a life science, • 6 or more years experience in Central Lab Project management, • Experience working directly with internal or external customers, • Strong relationship building and management skills, • Familiarity with clinical or preclinical research protocols, • Strong planning, organizational, and problem-solving skills, • Excellent verbal and written communication skills, • Excellent skills using computer applications (e.g. Windows, Excel, Word) In this role, you will interact with external clients regularly throughout all duties and responsibilities. As such, the Study Design Lead will be knowledgeable and experienced in study design techniques related to the creation and maintenance of protocol specific databases, as well as, the Statement of Work (SOW). At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Central Laboratory Services is part of a global contract research organization within Labcorp. We offer the world’s largest network of central laboratories and support global clinical trials testing. A common set of processes, procedures, and instrumentation is offered throughout our sites in Europe, Asia/Pacific, and the United States, allowing us to receive samples globally and provide more than 700 assays across all laboratory science disciplines. Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement. #J-18808-Ljbffr

• Develop and implement change management strategies aligned with organizational and transformation goals impacting Global Project Management, • Collaborate with leadership to integrate change management ac vi es into project and program plans, • Design and execute strategic communicate on plans tailored to specific projects and target audiences that promote change readiness and adoption, • Identify and engage key stakeholders to gain buy-in and support for change initiatives, • Participate in stakeholder meetings and workshops to gather input, provide updates, and address concerns, • Establish metrics and feedback mechanisms to measure the effectiveness of change and communication efforts, • Use data-driven insights to continuously improve change management and communication strategies, • Evaluate organizational readiness and define mitigation actions for change risks impacting Global Project Management, • Partner with Process Governance to assess impacts to operating models, roles, responsibilities, and processes, • Create communication materials and enablement assets, training strategies, and adoption tools to support change initiatives, • Establish and manage champion networks and support training delivery execution, • Establish mitigation plans for adoption, capability, and capacity risks, • Other duties as assigned. Bachelor's degree • 5 or more years of relevant organizational change management experience, • 2 or more years of hands-on experience delivering impact assessments, training, and communications, • 2 or more years of experience leveraging technology as an enabler of transformation, 1 or more years of experience managing workstreams or initiatives within large scale, complex transformations, • 1 or more years of experience managing senior stakeholder relationships, • Prosci Change Management certification, • Change Management Institute certification, • PMP, PgMP, Agile, or related project/program management certification, • Fluency in English, • Strong management expertise with knowledge of ADKAR or similar models, • Strategic thinking and ability to drive innovative solutions, • Excellent written, verbal, and presentation skills, • Strong stakeholder engagement and facilitation skills with senior leaders, • Strong project management skills with a track record of deliveries on time, • Analytical judgment, critical thinking, and problem-solving skills, • Adaptability, resilience, and ability to manage change in dynamic environments, • Proficiency with communication tools and virtual collaboration platforms., • Executive presence and influence without authority, • Strategic communication skills, • Organizational design awareness, • Data-driven decision making, • Facilitation and workshop leadership, • Conflict resolution and negotiation, • Business process transformation knowledge Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we’re improving health and improving lives. #J-18808-Ljbffr

A leading drug development company in Harrogate is seeking a Laboratory Analyst to join their BioAnalysis team. This role involves preparing samples for analysis, processing data, and writing standard operating procedures.

£29,000 - £33,000 + Training + Benefits + progression York Do you have a background in a production or manufacturing environment or similara? Are you looking to join an established business who are offering full training and opportunities to go through multiple courses to develop your technical skills and career? On offer is an exciting opportunity to join a well-established business where you will work closely with the Technical Manager to ensure quality, food safety and compliance standards are consistently maintained across the site. You will be involved in internal auditing, HACCP, microbiological testing, traceability and supporting both internal and external audits. This varied role will give you the opportunity to work across the factory, carrying out daily compliance checks, investigating non-conformances and customer complaints, maintaining quality documentation and supporting continuous improvement across the business. This role would suit someone from a production or manufacturing environment who is looking to join a well-established company offering full training and opportunities to go through courses to develop your technical skills and career. • Supporting the Technical Manager with the company's quality assurance and food safety objectives, • Carrying out daily compliance checks across factory departments and reporting non-conformances, • Conducting internal audits covering GMP, HACCP, BRC, hygiene, maintenance, factory fabric and quality systems, • Monitoring temperatures, air temperatures, data loggers and other quality control checks, • Carrying out pre-operation hygiene inspections across the abattoir and boning hall, • Collecting and coordinating microbiological samples, environmental swabs and meat samples for laboratory testing, • Background in a production or manufacturing environment or similar, • Looking for a full-time role, • Commutable to York Mon - Fri (6 am - 3.30 pm) Reference: BBBH27300A Keywords: Quality Assurance, QA, Quality Control, QC, Quality Technician, QA Technician, Technical Assistant, Food Safety, Internal Auditor, Compliance, Auditing, Food Safety Technician, Technical Assistant, York, Heslington, Holtby We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is intended as a guideline. The final package offered will depend on your experience, skills and qualifications. #J-18808-Ljbffr

Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives. Labcorp is seeking a remote Study Design Lead to join our Central Labs Services team in United Kingdom. • Accurately interpret and translate sponsor protocol requirements into the protocol specific database to generate a Statement of Work for the CLS project., • Leverage technical, therapeutic area, client, and company specific process knowledge to provide a comprehensive and complete database design., • Interact with external clients regularly through all duties and responsibilities., • Liaise with internal departments to understand full company capabilities and assess feasibility of requests to meet client needs related to study design., • Act as a consultant to advise on study design choices and work with the Global Study Manager (GSM) to highlight risks and budget impacts associated with study design., • Expand consultancy capability at study program levels., • Display strong interpersonal and communication skills that will build strong internal and external relationships to ensure high quality study design., • Coordinate internal processes and communications related to study design (including but not limited to internal feasibility requests, material transfer agreements and supply forecasting) and ensure the eventual follow up is integrated into the database and global monitoring plan., • Perform quality self-review., • Ensure that all customer requirements with relation to study design are documented and acted upon., • Act efficiently in an environment with dynamic timelines and priorities., • Display appropriate self-organization and ability to manage conflicting priorities., • Participate in functional meetings (e.g. Continuous Learning Forums (CLFs)) and provide input, keeping processes up to date., • Comply with our internal Central Lab Global Project Management strategy., • Manage a portfolio of global and local studies with varying complexities., • Support a culture of continuous improvement, quality, and productivity. Bachelor’s degree in a life science 6 or more years of experience working in the clinical research industry or within a lab environment Master degree in a life science 6 or more years experience in Central Lab Project management • Experience working directly with internal or external customers, • Strong relationship building and management skills, • Familiarity with clinical or preclinical research protocols, • Strong planning, organizational, and problem-solving skills, • Excellent verbal and written communication skills, • Excellent skills using computer applications (e.g. Windows, Excel, Word) In this role, you will interact with external clients regularly throughout all duties and responsibilities. As such, the Study Design Lead will be knowledgeable and experienced in study design techniques related to the creation and maintenance of protocol specific databases, as well as, the Statement of Work (SOW). At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Central Laboratory Services is part of a global contract research organization within Labcorp. We offer the world’s largest network of central laboratories and support global clinical trials testing. A common set of processes, procedures, and instrumentation is offered throughout our sites in Europe, Asia/Pacific, and the United States, allowing us to receive samples globally and provide more than 700 assays across all laboratory science disciplines. Labcorp is proud to be an Equal Opportunity Employer: Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. We believe in the power of science to change lives. Labcorp is a leading global life sciences company that provides vital information to help doctors, hospitals, pharmaceutical companies, researchers, and patients make clear and confident decisions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations to improve health and improve lives. Here, you can join our nearly 70,000 employees, serving clients in more than 100 countries, as we work together to transform approaches to patient care. #J-18808-Ljbffr

Smithers Ltd. in Harrogate is seeking a Laboratory Technician to join the Ecotoxicology Department. The role is lab-based, with duties including housekeeping, culturing organisms, and maintaining equipment and supplies. You will work as part of a team, with time split across the lab and related tasks. Training will be provided on degradation studies, sample analysis, data processing, and general lab duties. #J-18808-Ljbffr

Laboratory Technician – Immunochemistry Our largest UK site in Harrogate, North Yorkshire is currently recruiting for a Laboratory Techncian to join the Immunochemistry team. As a Laboratory Technician within our Immunochemistry team based in Harrogate, North Yorkshire you will play an integral pa

Labcorp in Harrogate, North Yorkshire, is hiring a Laboratory Technician to join the Immunochemistry team. The role focuses on routine equipment use, reagent preparation, and daily lab maintenance in a GLP-guided environment. You will contribute to study support, perform verifications, manage inventory, and uphold health and safety standards while developing skills in ELISA and ADA assays. This position is onsite. #J-18808-Ljbffr

A global FMCG manufacturer in Harrogate is seeking a Quality Assurance Technician to maintain Food Safety & Quality Systems. The ideal candidate should have experience in Quality Assurance or microbiology within food manufacturing. This is a full-time role that requires UK residency and involves conducting quality tasks in a laboratory setting. Excellent communication and organisational skills are essential, along with a degree in a relevant field. Competitive salary offered. #J-18808-Ljbffr

A global contract research organization is seeking a Laboratory Support Technician in Harrogate, England. In this role, you will conduct laboratory prep work, maintain equipment, and assist with various operational tasks. The position offers full training, competitive salary, and opportunities for career advancement in the scientific industry. Excellent attention to detail and teamwork skills are essential for success. Join a supportive environment where your contributions will help achieve important research goals. #J-18808-Ljbffr

Based in Harrogate, we are currently recruiting for a Laboratory Technician, ideally with previous GLP (Good Laboratory Practice) and/ or laboratory experience. The role is varied in nature and includes general housekeeping and cleaning, culturing and maintenance of organisms, routine maintenance of

Do you have a scientific degree and want to work in the scientific industry? Do you want to be part of the world's leading drug development company? Are you looking for a role with training and career progression opportunities? Labcorp Drug Development is a global, world-leading Life Sciences Contra

Whilst training you will learn a broad range of standard technical laboratory skills and techniques including how to work to Good Laboratory Practice (GLP). Washing, drying and sterilisation of laboratory glassware and consumables. Do you want to work in a laboratory?.

Matchtech is seeking an experienced Quality Control Laboratory Analyst to join their team in Petersfield. The ideal candidate holds a degree in a scientific discipline and has experience in a QC or laboratory environment.

United Kingdom National Nuclear Laboratory Limited is offering a CE&I Design Engineering Graduate opportunity based at the Sellafield site.

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

The business is looking for a Laboratory Technician to join its Technical Services Team and play a key role in the delivery of complex projects and bespoke fuel formulation. This is an opportunity for a technically minded Chemistry graduate with laboratory and project experience to take ownership of

This is an important role, working in the research team, you will perform various laboratory-based tasks such as mammalian cell culture, NGS library preps, cloning and DNA preps, etc. Aid in the smooth running of the laboratory. Perform routine laboratory activities such as colony PCR, Sanger sequen

UK National Nuclear Laboratory is seeking a Head of Enterprise Applications to lead the strategic direction of enterprise applications and data platforms across a heavily regulated organisation.

Established organisation operating within the clinical laboratory and diagnostics sector. Designs, supplies and supports specialist laboratory equipment. Field‑based role supporting modern laboratory equipment within clinical environments.

EMBL-EBI invites applications to contribute to data portals for leading sustainability and biodiversity projects.You will develop software for data curation, validation, distribution, and visualization, collaborating with large scientific communities to implement metadata standards and project-speci

You will join the InsectNeuroLab in the Department of Biosciences, Durham University ( ) that uses mosquitoes and other insects to study sensory neuroscience and sensory ecology.You will be responsible for the maintenance on mosquito and fly stocks and the insectary space.You will also contribute to

Maintain high laboratory standards and cleanliness, contributing to the laboratory’s overall success. Participate in laboratory projects as required by the business. At least 3 years of laboratory experience, including leading and motivating a team of technicians.

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

Our client is a leading provider of laboratory instrumentation and is now seeking a Lab supervisor to take responsibility for their demonstration laboratory, including equipment maintenance, calibration and safety compliance. Ensuring functional operation of the laboratory space and ensuring readine

Based in a fast-paced laboratory environment, you will help develop tailored analytical programmes and maintain accurate records in the LIMS, while escalating delays or issues as needed. Tetra Tech is recruiting a Project Coordinator for our Bedford laboratory to support complex analytical projects.

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 global nutrition company in the United Kingdom is seeking a Senior Laboratory Technician to lead a high-performance laboratory team. You will be responsible for ensuring the highest quality standards, coordinating laboratory operations, and managing microbiological and chemical analyses. The ideal

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

Laboratory testing and analysis. Interested in laboratory testing and food quality.

To be responsible for laboratory throughput and turnaround times, ensure all laboratory KPIs are met. Talk openly about laboratory performance and targets, with Directors and the laboratory team, to develop a strong, results-driven, team-oriented culture. At YorkTest, we have an exciting opportunity

There’s never been a more exciting time to be part of the nuclear sector.New opportunities are being created all the time.At UKUKNNL, you’ll be in the ideal place to capitalise on this momentum, face new challenges and develop a long, successful and meaningful career.UKNNL is where your solution

Leading and managing the laboratory team of 2-4 people. Ensuring compliance with standard operating procedures (SOPs), ownership of quality management system, and active contribution to fulfil regulatory and laboratory health and safety requirements. Laboratory Information Management System.

Senior Laboratory Research Scientist. Senior Laboratory Research Scientist, Pre-clinical ultrasound. We are now looking for a Senior Laboratory Research Scientist to join the in‑vivo imaging team.

Due to continued growth and an expanding national client portfolio, we're looking for an experienced and motivated P401 Qualified Laboratory Analyst to join our established UKAS-accredited laboratory in Halesowen. Part Time Afternoon Shift Qualified Laboratory Analyst. This is an excellent opportuni

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

Geotechnical Laboratory Technician. UKAS accredited geotechnical soil and materials laboratory based in. Suitable candidates will need to be able to demonstrate previous laboratory experience in this field.

You will perform laboratory testing that helps veterinarians diagnose and treat pets across the UK. Ideally, you will have experience working in a laboratory. Operating laboratory equipment (microscopes and/or clinical diagnostic analyzers) would be a plus.

RSK Group Ltd is seeking a Geotechnical Laboratory Technician for their UKAS accredited soil and materials laboratory in Washington, UK.

An exciting opportunity exists for a research laboratory technician to join the Lancaster Environment Centre (LEC). The Geophysical Fluid Dynamics (GFD) Laboratory in the Lancaster Environment Centre (LEC) is a world-class facility for research into a wide range of topics covering volcanology and pl

National Physical Laboratory (NPL) invites applications for a Platform Engineer within the Time & Frequency department.

United Kingdom National Nuclear Laboratory in England seeks a Project Manager to lead complex scientific projects, coordinating scientists, engineers and analysts to deliver cutting edge outcomes within schedule and budget.

We are looking for two Senior Laboratory Research Scientists to join the Chemical Biology Science Technology Platform at the Crick. Understanding of theoretical and practical enzymology and/or molecular pharmacology for the characterisation of recombinant targets, combined with a track record of hig

Applicants MUST have proof of immediate, on-going and valid eligibility, to work full time, and travel within, the UK*.I am currently recruiting on behalf of an automotive OEM, based in Wolverhampton, who are looking for a Lab Technician to join their team.As Lab Technician, your main responsibiliti