23 of 23 Good Clinical Practice Jobs in the South East

Research: Work and adhere to the principles laid down in the International Conference on Harmonisation, Good Clinical Practice Guideline (ICH/GCP) as well as Trust policies. To help ensure all patients consented to clinical trials at MARC are recorded on their individual Trust electronic medical … interpretation of data Skills in report writing Knowledge of ethical and quality standards applicable to clinical trials, including EU Directive on ICH GCP requirements Knowledge of the Health Service, R&D, the pharmaceutical industry partnership and relevant information sciences Knowledge of clinical audit methodologies, monitoring and action planning ...

Management Systems at MedPharm. The role is responsible for supporting compliance with Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), applicable regulatory requirements and internal quality procedures through the review of quality documentation, management of quality systems … metric reporting and trend analysis. General Build effective working relationships with internal departments, clients and external service providers. Maintain current knowledge of applicable GMP, GCP, GLP and regulatory requirements. Perform other duties appropriate to the position as requested by QA Management Key Relationships Heads of Departments Senior Management Production Pharmaceutical ...

Data Transfer Agreements and Data Management Plan drafting. Manage EDC access. Database design, set up, testing and maintenance. Ensure CDM activities conform to ICH GCP guidance. Lead and/or participate in internal and external audits of clinical data management processes. Essential EDC data entry and review. Generating data … Data Transfer Agreements and Data Management Plan drafting. Manage EDC access. Database design, set up, testing and maintenance. Ensure CDM activities conform to ICH GCP guidance. Lead and/or participate in internal and external audits of clinical data management processes. Desirable Assist with Data Transfer Agreements and Data ...

summary The NIHR Oxford Health Clinical Research Facility is seeking a Clinical Research Laboratory and Biostorage Coordinator to support the delivery of a diverse portfolio of research studies and the day-to-day operation of the CRF laboratory and biostorage service. The successful candidate will play … subject, or equivalent relevant knowledge and experience. Evidence of continuing professional development relevant to laboratory, research or biostorage practice. Desirable Relevant specialist training, e.g. Good Clinical Practice, Good Laboratory Practice, biological sample shipping or human tissue governance Experience Essential Significant practical experience in a research ...

accordance to departmental processes and procedures. This position is accountable for the planning, oversight and delivery of statistical programming activities supporting one or more clinical projects, compounds and/or submissions generally of low-medium complexity/criticality. The Senior Statistical Programming Lead is responsible for making decisions … Analytics, Biostatistics, Clinical Trials, Collaboration, Consulting, Critical Thinking, Data Privacy Standards, Data Quality, Data Savvy, Digital Fluency, Good Clinical Practice (GCP), Quality Assurance (QA), Report Writing, Standard Operating Procedure (SOP), Statistical Analysis Systems (SAS) Programming, Statistics, Systems Development, Technologically Savvy. At Johnson & Johnson, we believe health ...

with departmental processes and procedures. This position is accountable for the development, verification, and documentation of code used for the analysis and reporting of clinical data and is responsible for the timeliness and the quality of assigned deliverables supporting clinical projects and submissions. This position is a member … Reasoning Biological Sciences Biostatistics Clinical Trials Data Modeling Data Privacy Standards Data Quality Data Savvy Detail-Oriented Good Clinical Practice (GCP) Report Writing Research Ethics Researching Statistical Analysis Systems (SAS) Programming Statistics Technologically Savvy #J-18808-Ljbffr ...

requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Responsibilities: Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables … Data Manager and Study Leader. Education and Experience: Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have ...

requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Key Responsibilities: Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables … Data Manager and Study Leader. Education and Experience: Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience; Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have ...

within the pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience in generating and validating SDTM, ADaM, and TLFs Good understanding of CDISC standards and clinical trial processes Ability to work independently and manage multiple priorities in a fast-paced environment Experience supporting … regulatory submissions is preferred Strong communication and stakeholder management skills Responsibilities: Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Create datasets, tables, listings, and figures according to study requirements Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards ...

within the pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience in generating and validating SDTM, ADaM, and TLFs Good understanding of CDISC standards and clinical trial processes Ability to work independently and manage multiple priorities in a fast-paced environment Experience supporting … regulatory submissions is preferred Strong communication and stakeholder management skills Responsibilities: Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Create datasets, tables, listings, and figures according to study requirements Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards ...

industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience supporting regulatory submissions is preferred Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards and project timelines Participate … study planning, review specifications, and support submission activities Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master's degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Working knowledge ...

industry Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies Experience supporting regulatory submissions is preferred Develop, validate, and maintain SAS programs for clinical study data analysis and reporting Collaborate with Biostatistics, Data Management, and Clinical teams Ensure programming deliverables meet quality standards and project timelines Participate … study planning, review specifications, and support submission activities Bachelor's degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master's degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Working knowledge ...

This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables … Statistician, Lead Programmer, Data Manager and Study Leader. Bachelor s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have ...

This position requires high technical skills and thorough industry knowledge to independently perform the Programming tasks Responsible for supporting the Programming deliveries of a clinical study or project. Implements statistical programming aspects of the protocol and the clinical development program. Ensures high quality is built into own deliverables … Statistician, Lead Programmer, Data Manager and Study Leader. Bachelor s degree in computer science (CS), statistics, or related scientific disciplines with 5 yrs. of clinical programming (CDISC) experience Master s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have ...

pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have Respiratory/Immunology TA experience. Working knowledge of ICH and Good Clinical Practices, Clinical research … Clinical trial process, and related regulatory requirements and terminology. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately ...

pharmaceutical/CRO industry Hands-on experience supporting CVRM (Cardiovascular, Renal Master’s degree in CS, statistics or related disciplines with 6 yrs. of clinical programming (CDISC) experience. Need to have Respiratory/Immunology TA experience. Working knowledge of ICH and Good Clinical Practices, Clinical research … Clinical trial process, and related regulatory requirements and terminology. The Application Process Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately ...

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 … RNAi. Desired Experience Experience in clinical development through Phase 3 (NDA submission). Experience as lead statistician for a compound Understanding 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 ...

than 60 years developing innovative respiratory diagnostic solutions that help healthcare professionals detect, diagnose and manage respiratory conditions. We are now recruiting for a Clinical Equipment Support Technician to join our team. This is an exciting opportunity to become part of an established global healthcare organisation, working hands … within the Warehouse. Competence in Vitalograph procedures and the Quality Management System (QMS). An understanding of ISO 13485, the Medical Devices Directive and GCP, as required. If youre looking for a hands-on role where you can develop your technical and healthcare knowledge, work alongside experienced teams and build ...

execution of programs in statistical programming languages within project. Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for inclusion in clinical reports or presentations. Create complex programs that meet regulatory and company standards to permit efficient programming, reporting, and review, utilizing statistical programming languages (e.g … relationship skills including consultative and relationship management skills. Full understanding and knowledge relevant to statistical programming. Full understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device setting. Strong problem-solving, organizational, analytical and critical thinking skills. Experience working in clinical ...

Data Acquisition Specialist performs activities relating to the definition, set-up and ingestion of External Data Streams, and related documents and processes aligned with Clinical Trial Protocol defined requirements for data capture. External data streams include but are not limited to typical and novel data collected through central labs … clinical trials. Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional. Knowledge of SDTM. Working knowledge of GCP/ICH guidelines Excellent written and verbal communication in English. This role is not eligible for UK visa sponsorshipIQVIA is a leading global provider of clinical ...

Perspectum Ltd is seeking a Clinical Data Manager I responsible for ensuring trial data is accurate, complete, and aligns with study protocols and SOPs. You will collaborate with clinical operations, biostatistics and medical writing to support collection, management and analysis of data. You are detail-oriented with … passion for clinical research and data management. The role involves EDC data entry, data queries, database design and participation in quality audits in line with ICH GCP. #J-18808-Ljbffr ...

oversee programming activities across one or more clinical projects. You will guide a team of programmers, ensure on-time delivery and compliance with GCP and SOPs, and contribute to study design and data analysis strategies. The role emphasizes advanced analytics, collaboration with cross-functional teams, and delivering high-quality ...

statistical programs for clinical data, supporting analysis and reporting with high quality deliverables. You will collaborate with cross-functional teams, ensure compliance with GCP and internal processes, and help drive efficiency through robust programming practices and documentation. #J-18808-Ljbffr ...