26 to 50 of 60 Good Clinical Practice Jobs

Proclinical is seeking a dedicated Manager of Global Trial Optimisation. This role involves overseeing the clinical development strategy, clinical study concepts and protocols as well as operational plans. The successful candidate will play a crucial part in maintaining relationships with external experts to facilitate a wide source of … to meet deadlines, effective use of time, and prioritization. - Ability to influence and negotiate across a wide range of collaborators. - Knowledge of ICH/GCP and regulatory guidelines/directives. - Advanced project management skills, cross-functional team leadership, and organizational skills. - A minimum of a Bachelor's degree and relevant … industry experience. - Direct experience managing global clinical trial operations, including experience developing protocols and key study documents. - Technical proficiency in trial management software and MS applications. Interested or know someone who might be? Reach out to ­­­­Matthew Pike using the following: ✉️ m.pike@proclinical.com 📞 +44 207 4400 639 (5342) Apply more »

of Quality Assurance is to promote a quality culture of continuous improvement to ensure all systems and procedures undertaken are in compliance with ICH-GCP guidelines and other regulatory requirements. Main Responsibilities Ensure Non-Conformances/Incident Reports are reviewed, assessed and approved using the eQMS ensuring it is contributing … to continual quality improvement. Ensure Quality Documents are reviewed for process improvements, are of a high standard in accordance with ICH-GCP, and approved using the eQMS. Ensure external Sponsor audits or Inspections are prepared, hosted including timely provision of document requests, and for any findings CAPAs are raised, reviewed … necessary. Organising QA training for all staff - including distributing workload and monitoring task completion. Qualifications and Experience: At least 6 years of experience in GCP Quality Assurance within the Pharmaceutical Industry. Strong knowledge of Quality Management Systems within the Pharmaceutical industry. Strong knowledge of ICH-GCP and GMP guidelines. Experience more »

Assurance department. - Knowledge of GxP and Quality related regulations and standards within the Pharmaceutical/Medical Device industry. - Familiarity with ISO 9001, ISO 13485, GCP is essential. - Knowledge of ISO 21CFR Part 820, ISO17025, Clinical Trials experience, ISO13485 Lead auditor would be beneficial. Interested or know someone who might 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 »

involved in NHS, academic and commercial research. The post involves high volume, face to face contact with patients, principally in the glaucoma service acquiring clinical diagnostic data to support and inform clinicians. The post holder interacts routinely with: patients, administrative, clerical, technical and clinical staff within the Trust … date professional development plan Desirable AOSP/ACHS Registration Previous technician certification for multicentre/international clinical trials Member Ophthalmic Imaging Association Current GCP Certification/NVQ 3equivalent Experience Essential Experience in ophthalmic imaging/retinal screening Evidence of recent professional development. Desirable Experience in a commercial photographic environment. more »

s Hospital, Royal Brompton and Harefield - as well as community services in Lambeth and Southwark, all with a long history of high-quality care, clinical excellence, research and innovation. We are among the UK's busiest, most successful foundation trusts. We provide specialist care for patients including heart and … as well as a full range of local hospital and community services for people in Lambeth and Southwark. We have a long tradition of clinical and scientific achievement and - as part of King's Health Partners - we are one of England's eight academic health sciences centres, bringing together … world-class clinical services, teaching and research. We strive to recruit and retain the best staff as the dedication and skills of our employees lie at the heart of our organisation and ensure that our services are of the highest quality, safe and focused on our patients. Job description more »

The IVD Clinical Research Associate will design, plan, coordinate, and conduct all activities involved in initiating, monitoring, and completing clinical research studies for in vitro diagnostics. Responsibilities include but are not limited to: * Ensuring studies are conducted and documented in accordance with the study protocol, standard operating procedures … good clinical practices and other applicable regulatory requirements; * Validating product performance claims; * Supplying data for critical Regulatory submissions; * Defining the functional and clinical utility of investigational products, and * Obtaining opinions and input regarding investigational products from laboratories or customers, who may be considered key opinion leaders. The … adhering to the policies of the quality system and achieving quality objectives through daily actions. JOB FUNCTIONS/RESPONSIBILITIES * Performing or coordinating aspects of clinical studies including site selection, study initiation, site monitoring, and study closeout. Maintaining communication with study investigators to ensure studies are completed in a timely more »

to improve the health and wellbeing of the people we care for, as well as supporting andempowering them to lead a fulfilling life. Our clinical teams deliver many NHS services, not only via inpatient and primary care settings, but also within the community. These services include children's, adult … Qualifications Essential Post graduate qualification in a field relevant to research A degree in law or equivalent qualification Desirable Evidence of continuing professional development GCP Trained Knowledge & Skills Essential Knowledge of clinical research governance Ability to communicate, negotiate and influence effectively as appropriate at all levels and be persuasive … Experience Essential Experience of working with contracts Experience of negotiating contracts in a life science or research setting Desirable Experience of working in a clinical research environment in an NHS Trust, University, pharmaceutical company, charity or other organisation Experience of analysing and interpreting complex contractual terms and/or more »

is currently collaborating with a CRO, who are actively seeking a Head of Quality Assurance to oversee and uphold the highest standards within our clinical research processes. In this pivotal role, you will lead a dedicated team committed to maintaining excellence and … driving continuous improvement. Your responsibilities will include ensuring that our operations align with the rigorous standards outlined in Good Clinical Practice (GCP) guidelines and regulations. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Create … within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with excellent communication, collaboration, and interpersonal skills. Detail-oriented with strong analytical and problem-solving abilities. Proven ability to drive more »

Job summary Are you an enthusiastic individual who is looking for a new challenge in Clinical Research? Do you want to make cutting edge clinical research available to a wider range of people? Do you have an inquisitive mind? If so, we would like to hear from you … our team for 12 months . A secondment is possible, if approved by your current manager. BCHFT is a Mental Health Trust, and our Clinical Research portfolio of studies covers all services, including Eating Disorders, LearningDisability, Memory Assessment, IAPT, Early Intervention, Autism and many more. Main duties of the … manage workload Desirable Awareness of clinical research governance issues, including risk management, and ability to resolve queries Good Clinical Practice (GCP) knowledge Skills/Personal qualities Essential Excellent spoken and written communication skills, including the ability to articulate information concisely, accurately and accessibly Ability to develop more »

debilitating disease areas. Our guiding principles, centred around Integrity and Patient-Centricity, are at the heart of everything we do. Job Purpose Lead all Clinical Data Management (CDM) lifecycle activities from protocol inception to database delivery for numerous global studies via oversight of multiple vendors and internal/external … database locks. Participates in Service Provider selection, evaluation and management, including reviewing and providing input to scope of work. Coordinates user acceptance testing for clinical databases. Contributes to global and sub functional working groups and initiatives. Responsibilities Responsible for delivery of clinical global study databases and specific study … is an essential part of the position Working as the sole Data Manager within the Team Key skills and experience In depth knowledge of GCP and current legislation. Working knowledge of Medidata Rave ( desirable but not essential) and IBM databases Experience of delivering global clinical studies across different phases more »

via literature searches. Providing an indication of any potential difficulties with bioanalytical methods and assisting with client calls and visits. Working to GLP/GCP and showing good documentation practice. The Person A successful candidate will have previous experience working in a regulatory bioanalysis lab with experience performing LC … experience of using LC-MS/MS. Previous experience of troubleshooting Have previous experience performing sample extraction techniques for biological analysis. Must be a good communicator with excellent interpersonal skills. Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this more »

you to have: BSc/MSc/PhD in Chemistry (or related scientific discipline) A sound working knowledge of relevant quality standards; GMP, GLP, GCP and other analytical related quality standards Good working knowledge of Quality Assurance in the Chemical and Pharmaceutical Industry Quality Assurance background which includes some … attention to detail Impressive written and verbal communication ABOUT THE OPPORTUNITY You will provide general support to Quality Assurance activities relating to GLP, GMP, GCP, and other similar Quality Systems established to ensure that the appropriate standards and effective working systems and relationships are maintained and where necessary improved. Responsible … for auditing GLP, GCP and GMP plans, raw data, study procedures and related facilities to ensure compliance with current relevant regulatory requirements and internal consistency, Identify and report any areas of non-compliance to both study and facility management. Liaise with key stakeholders, providing them with accurate information and progress more »

Job summary An exciting opportunity has arisen for a Specialist Clinical Trials & Cancer Services Pharmacist to join the Cancer and Aseptic Services team at ESHT. The successful candidate will lead on a portfolio of cancer & non-cancer clinical trials undertaken … within ESHT. They will appraise all relevant clinical trials & offer pharmaceutical input in accordance with legal requirements & Good Clinical Practice (GCP) relating to the prescribing, handling, dispensing, administration, storage & disposal of investigational medicinal products (IMPs) & non-investigational medicinal products (NIMPs). They will also contribute to … the delivery of a high quality specialist clinical pharmacy service to cancer clinical services. Experience in Cancer &/or Aseptic Services is essential. They will not only have the opportunity to explore & enhance their clinical expertise, but will also be developing management, training & leadership skills. They will more »

us You will join a small pharmacy-based team, where you will help to ensure the standards of Good Clinical Practice (GCP) are followed and that patients who volunteer to take part in clinical trials feel valued and receive an excellent pharmacy service. You will work … Operating Procedures (SOPs). To prepare invoice requisitions for clinical trial fees and monitor the receipt of income for specific trials. To attend GCP training as required by the Trust and to work to GCP standards at all times. To attend meetings regarding the set up and running of … Level 3 Pharmacy Services, BTEC Pharmaceutical Sciences or equivalent Registered Pharmacy Technician with the General Pharmaceutical Council Accredited Checking Pharmacy Technician (ACPT) qualification Desirable GCP training Skills and Experience Essential Good understanding of Clinical Trials Experience of working in a hospital pharmacy Evidence of working in a team more »

Manchester Childrens Hospital. As the Paediatric BMT Data Manager you will be responsible/for the high quality capture, processing and submission of complex clinical data from clinical systems within the Trust, ensuring the data is handled in a timely manner in line with EBMT recommendations. This includes … Operating Procedures (SOPs) with respect to the Data Protection Act, the Freedom of Information Act and ICH Good Clinical Practice (ICH GCP). To work alongside other Data Managers and Data administrators with the data entry and configuration tasks necessary to support the BMT Electronic Database (Access … Operating Procedures (SOPs) with respect to the Data Protection Act, the Freedom of Information Act and ICH Good Clinical Practice (ICH GCP). To work alongside other Data Managers and Data administrators with the data entry and configuration tasks necessary to support the BMT Electronic Database (Access more »

Job summary We are looking for a dynamic and enthusiastic clinical pharmacist, looking to expand their knowledge and experience in clinical trials. If you have not worked in clinical trials before but would like to gain experience, then please apply. You will join a high-profile dedicated … healthcare professionals and other agencies relating to pharmaceutical aspects of clinical trials. To understand EU and UK Clinical Trial legislation relating to GCP, GMP and medicines management and ensure incorporation into the implementation of new clinical trials. To deliver specialist education and training in Clinical Trials … risk assessments. To work with and support the pharmacy team working within clinical trial implementation at UHCW. Assisting the team undergoing statutory MHRA GCP inspections and implement corrective or preventative actions. Assisting the development of policies, guidelines, audits and research relating to the use of medicines and devices within more »

Job summary The post holder will lead the provision of a high quality, safe and effective pharmacy clinical trials service, to ensure compliance with the required National Standards and UHBResearch and Development Strategy. The post holder will be the Pharmacy Lead Facilitator for Research and Audit projects. They will … own professional actions and deliver a high quality specialisedclinical pharmacy service to promote the safe, rational and cost-effective use of drugs,through personal practice and the training of other staff. The post holder will contribute to the training and education for Undergraduate HealthProfessionals and Post-Graduate Pharmacists, Nurses … Health Board's Research & Development department and, supported by our highly experienced Senior Pharmacy Trials Technician, will provide expert regulatory knowledge with regards to GCP and pharmaceutical aspects of clinical trial delivery and management. The ideal applicant will be a highly motivated and methodical pharmacist who is able to more »

Within pharmacy we have a position for a senior assistant technical officer. We are looking for an enthusiastic person to join our small pharmacy clinical trials team. We are responsible for ensuring that all the pharmacy and medicine aspects of clinical trials for cancers are conducted according to … daily basis providing feedback to relevant individuals as necessary. Management of IMP stock levels to include ordering, receiving, relabelling, archiving, according to Sponsor and GCP requirements To undertake routine expiry date checks and maintain the expiry date database. Arrange and act as a pharmacy representative at trial monitoring and close … field telephone calls and enquiries as appropriate. Person Specification Qualifications Essential NVQ 3/equivalent GCSE or equivalent passes in Maths, English and Science GCP training within last 2 years Desirable Excel and use of Microsoft office programmes Experience Essential Experience of using a variety of IT packages to include more »

job The main purpose of the role is all set-up aspects of clinical trials, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and trust policies. The post holder will assist with the administration of clinical trials from feasibility to archiving including (but … complex workload activity with prioritisation, referring to the Research Manager as necessary.To have an understanding that all research must be conducted according to ICH-GCP, the EU Directive on Good Clinical Practice and the Research Governance Guidelines and assist the team in upholding these. About us At … computer skills, excellent oral and written communication skills. Attention to detail. Knowledge Essential Technical Professional Detailed knowledge of the clinical trials process and GCP guidelines/EU Directives Understanding of medical terminology. Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order more »

Job summary Clinical Specialist Radiographer/Technologist - PET-CT & CT OR Clinical Specialist Technologist - PET-CT London Location: Leaders of Oncology Care (main location) and The Harley Street Clinic Hours: Full Time 37.5 hours per week Shift times: 7.5 hour shifts Monday-Friday Salary: Up to … in particular Radiation Protection and Infection Control To assist with patient bookings and administrative duties where necessary To support departmental audits in accordance with clinical governance policies To ensure that quality assurance of equipment is carried out in line with departmental policy, recording and report faults in a timely … To assist with the implementation of new policies within the department and monitor their effectiveness To maintain a high standard of patient care through good clinical practice. About us At The Harley Street Clinic and Leaders in Oncology Care, we provide a range of complex care services, specialising more »

Description: Our client, a leading global clinical trial laboratory services organization providing focused on comprehensive testing, project management, supply chain, biorepository and specimen management, and clinical trial sample and consent tracking solutions is … seeking Associate Scientists top support their vaccine laboratory and the vaccine development life cycle. Skills: pipetting, cell culture, cell based assay, aseptic technique, gdp, gcp, glp Top Skills Details: pipetting,cell culture,cell based assay,aseptic technique Additional Skills & Qualifications: At minimum 1 year of directly related industry experience BS … Degree in Biology, Microbiology, Molecular Biology or other closely related field Cell Culture/Cell Based Assay experience is a MUST GLP/GCP/GDP Experience Preferred Experience Level: Intermediate Level About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary more »

the technical services team at Sheffield Teaching Hospitals. Currently housing 11 pharmaceutical isolators with another 4 due imminently within the cutting edge ATMP/clinical trial facility being developed within Weston Park, prospective candidates have a unique opportunity to be at the forefront of technical services in a large … the country, offering a range of both general and specialist hospital services. We provide nationally commissioned services and expertise in support of Early Phase Clinical Trials, and we are part of a leading national network for the development of cancer drugs of the future (Experimental Cancer Medicine Centre). … in Pharmacy Post-graduate Clinical Diploma or equivalent demonstrable experience. Desirable Independent Pharmacy Prescriber (IPP) status Pharmaceutical Technology & Quality Assurance (PTQA) course qualification. GCP certificate Band 8a - Experience in a Qualified Person (QP) role. Experience Essential Post registration experience of sufficient quality and quantity to enable demonstration of achievement more »

ability to network and build strong relationships, experience of building and maintaining EPMA systems and a passion to foster integration of the digital and clinical workforces will be essential. This post is ideally suited to someone with extensive digital experience, as well as a strong grounding in clinical practice, who is motivated by well managed change across traditional professional boundaries. The postholder will lead on all aspects of the digital portfolio including our IT systems and will be supported by a team of well-developed pharmacists, technicians and support staff. You will be a role model … to the development of strategic plans for specific areas of IT (procurement/commerce; digital medicines). Contribute to the development and implementation of Clinical Trials as required. About us All new colleagues can expect to receive a warm and friendly Wirral welcome from the very first time they more »

Trial administration duties such as filing, kit inventory, booking couriers, research data entry, data presentation and assist in trial co-ordination in compliance with Good Clinical Research Practice. Main duties of the job To function as a member of the Trials team through provision of dedicated administrative support … to the clinical trials team. Working in a team to co-ordinate data collection for a caseload of patients participating in local, national and international trials in various treatment modalities and disease types. Disseminate information to consultants regarding new trials (including those on the NIHR Clinical Research Network … of the team. Provide support to other colleagues as required. Person Specification Education and Qualifications Essential BSc Life Science degree GSCE standard or equivalent GCP qualification Knowledge and Experience Essential Knowledge and experience with Multidisciplinary team and internal & external stakeholders Previous experience within haematology-oncology; or research Communication and Relationship more »