As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over … Fortrea is transforming drug and device development for partners and patients across the globe. Job overview: Provides strategic direction and oversight of Quality Assurance GCP Audit and Inspection operations and assures that audit program aligns with global RCQA strategies. Oversees external sponsor and inspectorate evaluations assuring follow up on trends … drive strategic business process improvement initiatives Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. more »
Company description: QA Director Audit & Inspection GCP-CDCS As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across … process improvement initiatives What we offer: Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. more »
inclusive of sample preparation, data acquisition and processing, and generation of development reports. ATTRIBUTES: A minimum of 3 years of study management experience in clinical and/or preclinical studies Strong background knowledge of … large molecule analysis in support of PK and PD studies. Experience working in a regulatory environment, managing studies that are compliant with GLP/GCP Experience in a client facing role with the ability to provide high level advice and guidance to clients Non-Smoker: due to the nature of more »
Are you already working in a GLP/GCP environment and want to consider Quality Assurance as your next career move? Do you want to be part of a company that helps build a healthier and safer world? Are you looking for industry recognised training and development opportunities? Labcorp is … equivalent Life Science experience) Experience may be substituted for education Skills/Experience: Proven work history in a regulatory environment working to GLP/GCP Ability to apply basic relevant regulatory knowledge Ability to follow instruction e.g. QA documents (SOPs) Ability to assimilate/interpret operational documents such that audit more »
Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that … programs. Position overview ProPharma are currently supporting one of the global leaders within the life-sciences sector as they require substantial support for their GCP auditing activities. At present, we are currently searching for a freelancer/contractor to work for them on a full-time basis (1.0FTE) remotely with … for 2025. Qualifications required Further education is required to at least a BSc level in a life science or related field Demonstrated background in GCP Quality/Auditing within the Pharmaceutical or Biological industry is a must Fluency in English is a must Ability to travel to sites within the more »
/life balance. What we are looking for Life science degree. Extensive auditing experience in GCP. Thorough knowledge of GCP. Able to confidently audit GCP Vendors or Investigator Sites with limited oversight. Strong client focus. What You’ll Do With Us Focusing on delivering top-class audits to our list more »
bioanalytical study or other plans Team player Review and sign of study data Responsible for regulatory compliance as assigned Ensure all processes are following GCP/GLP Liaising with clients regarding within agreed timescales Qualifications At least 3 years experience working in a regulatory bioanalytical laboratory. A degree in life … sciences or chemistry-related subject A good communicator with strong interpersonal skills. Experience working within a GLP/GCP accredited facility. Flexible and adaptable with an eye for detail Hand-on experience of LC-MS/MS, Sciex and Waters LC-MS/MS systems is an advantage Experience more »
you'll benefit from a scale of opportunity that is nothing short of extraordinary. We've also created a digitally enabled organisation to improve clinical quality, patient & staff experience, operational effectiveness & driving research, and innovation through the introduction of Hive; our Electronic Patient Record system which launched in September … this post but the post-holder will work closely with Partner organisations across the BRC and from across Greater Manchesters R&I academic and clinical ecosystem. The NIHR Manchester BRC works closely with other NIHR infrastructure in Greater Manchester including the NIHR Manchester Clinical Research Facility, NIHR Manchester … delivery. Experience of analysing complex data to assess risk and monitor progress against plans, managing deviations and issues appropriately to ensure successful project delivery. GCP trained Comprehensive IT skills (including MS Word, Excel, Powerpoint, databases, Internet and email). Ability to influence and negotiate with different professions and organisations and more »
University College London Hospitals NHS Foundation Trust
quality patient care. This post will also be committed to developing the research portfolio and enhancing the national and international profile of the service. Clinical work will be both outpatient-centred in the UCH Macmillan Cancer Centre and involve inpatient attending on a rotational basis. Participation in regional and … working closely with the CAR-T service alongside Dr Claire Roddie, Dr Maeve O'Reilly and Dr Paul Maciocia. There are 3 Cell Therapy clinical nurse specialists (CNS), 3 Lymphoma stem cell/CAR-T CNS and 10 ATIMP clinical trials nurse/practitioners. There is currently one … Participation in clinical audit and attendance at appropriate courses. Research Essential Familiarity with clinical trial methodology Evidence of research activity Evidence of GCP training Desirable Research in relevant clinical field Evidence of first authored publications/peer reviewed publications Disclosure and Barring Service Check This post is more »
Company description: QA Director Audit & Inspection GCP-CDCS As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more »
Advanced Clinical is seeking a Global Senior Manager in Feasibility to work for a European-based Global Biotech specializing in Oncology. The Senior (Snr) Manager, Feasibility, will support early evaluations for proposed new studies originating within the Sponsor. The Senior Manager, Feasibility, will undertake evaluations to determine whether a … location of patient populations, local practices, considerations of protocol designs, Site ID, and risks. Cross-functional working (e.g. with real-world evidence team, GPSS, Clinical Monitoring team) to facilitate processes to support therapeutic landscape evaluations to assist in the selection of best countries/sites to ensure the necessary … in evaluating the study viability. Required/Preferred Education Extensive pharmaceutical or related industry experience, minimum 8-10 years industry experience. Excellent knowledge of GCP and regulations Experience of team management more »
Biotech companies, are hiring a Senior Statistician to join their growing team. The role Lead and manage customer projects ensuring high-quality deliverables Analyse clinical trial data and real-world data Support HTA submissions Mentor junior colleagues Requirements 2+ years’ experience as a Statistician Industry experience, ideally working in … in the UK without needing visa sponsorship. Keywords: HTA, health technology assessment, statistician, biostatistician, ITC, indirect treatment comparison, NMA, network meta-analysis, ICH/GCP, SAS programming, R programming more »
HQ 💰 Up to £95,000 per annum 🦸Tech for Good 📈 Seed Funded Startup with thousands of users 📱 Tech Stack: React Native, TypeScript, ReactJS, GCP Play a meaningful, Senior role in building a product from zero to one as this tech for good start up scales from one product … team to many.. Sound interesting?.. This could be for you! I am partnering with a "Tech for Good", seed funded startup with ambitious plans to provide a long term, sustainable solution for one of life's taboo challenges related to sexual wellbeing. The aim being to provide a … large scale, cross platform applications in React Native. The role also opportunities to work across the stack with technologies such as TypeScript, ReactJS and GCP within an agile environment. You'd be involved in the end to end design and greenfield development of a React Native application with a focus more »
centre for children's health research with the goal of giving all children and young people the opportunity to participate in, and benefit from, clinical research. The Clinical Research Division works with our clinicians, academia, and industry to invent, develop, and test new treatments for children and young … Premier MRI scanner. The post holder will be required to work as part of a multi-disciplinary team and deliver high-quality research and clinical imaging in the Cross-Sectional service for a variety of paediatric and adult presentations. The post holder must have a flexible approach to the … the demands of the department and of research trial participants. Please see attached job description for further detail. Person Specification Requirements Essential HCPC registration GCP Certificate Degree/Diploma in Diagnostic Imaging Significant experience as a Senior Radiographer Desirable CSI Experience MRI Research Paediatric experience Disclosure and Barring Service Check more »
enthusiastic, self-motivated, organised quality professional with a keen eye for detail. Some previous experience (ideally between 1 - 2 years) of working in a GCP regulated environment or in a quality environment in a clinical trial organisation is desirable. Day to day, you will oversee the Companys quality systems more »
