1 to 18 of 18 Good Clinical Practice Jobs in London

Job summary The Liver clinical trials team at King's are inviting applications for a clinical trials data manager to work alongside the clinical trials team on an exciting portfolio of commercially funded and investigator led studies in liver diseases. The successful applicant will be an enthusiastic … . Responsible for the collection, co-ordination and computerisation of data generated from the clinical trials. Implement and adhere to the principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. Liaise with and assist the medical team/sponsor organisation … . Responsible for the collection, co-ordination and computerisation of data generated from the clinical trials. Implement and adhere to the principles of GCP (Good Clinical Practice) as set out in the Clinical Trials Regulations. Act as a resource and support to patients and their more »

Senior Project Clinical Data Manager We have the pleasure of working with a fantastic early phase CRO based in London. The company have a strong leadership team who are accelerating growth and have a great vision for the future. The offices are very modern and they have a fully … primary Data Management Lead for assigned projects ensuring clinical projects are carried out by the company in accordance with the executed contract, ICH GCP and other relevant regulations and guidelines and the customer’s expectations, taking responsibility for resourcing and planning of assigned projects. Provide hands on technical data … RFP) and Request for Information (RFI) process. Prepare input and participate in bid defence meetings Essential Degree or equivalent Knowledge of current regulatory regulations, GCP, ICH guidelines and Data-management industry standards SAS programming Detailed experience of end to end Clinical trial and Project Data Management processes, as well more »

Proclinical is seeking a dedicated individual for the role of Associate Director, Clinical Data Management. The successful candidate will be responsible for leading the team and overseeing the execution of clinical trials. Responsibilities: - Organise and conduct team meetings. - Foster team development and identify high-performance team members. - Collaborate … with the (Senior) Director Clinical Data Management on team development. - Provide guidance to project teams on the oversight and supervision of CRO/third party vendors and organize trainings as needed. - Act as a mentor for new team members. - Contribute to the development and review of portfolio documents (includes … Clinical Data Management with a focus on DM activities as a Lead and DM project management. - In-depth knowledge of international guidelines (ICH-GCP) for the conduct of clinical research projects. - Experience with Clinical Database Systems and processes. - Proven experience in resource planning. - A background in natural more »

the life sciences industry (CRO, pharmaceuticals, biotechnology, etc). The ideal candidate will possess a deep understanding of Good Clinical Practice (GCP) and its application in research studies. In addition, they will have proficiency in industry-standard clinical database applications, such as Electronic Data Capture (EDC … and Clinical Trial Management Systems (CTMS). Experience with programming languages like JavaScript or SQL is a strong plus. Company: CYTE is a full-service cardiovascular contract research organisation (CRO) powered by an integrated Clinical Research Platform and a Global Site Network. We provide research solutions to our … services. Role & candidate profile: Clinical Data Manager will ensure CYTE studies are planned and implemented to the highest standards, in compliance with ICH-GCP guidelines, CYTE SOPs and all applicable regulatory guidelines. Responsibilities: CRF design, database specification and edit check specification creation based on study protocols. EDC build and more »

Proclinical is seeking a dedicated and proactive Director of Clinical Compliance. This role focuses on establishing and implementing a Quality Strategy for clinical development activities. The successful candidate will ensure all work is in agreement with regulatory requirements and will adherence to Good Clinical Practices. This … alternatively can be a hybrid working role based in Mainz, Germany. Responsibilities: Provide strong QA leadership, fostering organizational awareness and interdepartmental collaboration. Implement the Clinical Development Quality Plan within the development portfolio. Provide robust quality oversight in various areas, including risk detection and remediation. Offer guidance on day-to … CAPA preparation. Lead a team to ensure a unified approach to proactive support for clinical trials. Key Skills and Requirements: Experience in a GCP Environment within the Pharmaceutical or CRO Industry. In-depth knowledge of worldwide regulations (including FDA, EMA) related to clinical development and post-approval. Experience more »

lives. Responsibilities: Drive risk-based approach to solve complex business problems. Provide expert input to functional teams in areas such as Biostats, Data management, Clinical Trial Supply and Logistics, IRT, Pre-clinical, CMC, Clinical Pharmacology, Translational Sciences, Medical Affairs, Commercial, Regulatory Affairs and Companion Diagnostics. Drive change … Skills and Requirements: Significant understanding within GxP operational and quality roles. Operational experience in at least one of the following areas: Biostats, Data management, Clinical Trial Supply and Logistics, IRT, Pre-clinical, CMC, Clinical Pharmacology, Translational Sciences, Medical Affairs, Commercial, Regulatory Affairs or Companion Diagnostics. Strong and … development and development of medical devices is a plus. Strong knowledge of Clinical Development and Research operations and regulatory landscape. Deep knowledge of GCP, GLP, GPVP, GCP for Labs and a general understanding of GMP. Expert in process development, industry standard problem-solving approaches, in alignment with Lean and more »

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 »

all the non-cancer non haematology beds, alongside the non resident general fellows. Main duties of the job Work closely and collaboratively with the Clinical Site Team, Modern Matrons, AHP and Nursing teams, as well as the ITU Fellows, Outreach team, Oncology Fellows and other Speciality Clinical Fellows. … Provide clinical support to the relevant Consultants, and be responsible for the clinical care of patients ensuring all in-patients on your allocated ward/s are reviewed daily and undertaking documentation, escalation when needed, as well as ensuring fluids/antibiotics etc are written up, and supporting … to audit, Quality Improvement workstreams, M&M, Risk, Complaints and Quality meetings and the reports/investigations that feed these meetings working with Divisional Clinical Director, Medical Director and Resident RMOs About us The London Clinic is one of the UK's largest private hospitals, where we pride ourselves more »

Training Essential Educated to degree level in relevant scientific discipline or equivalent Postgraduate qualification Experience/Knowledge Essential Regulatory requirements pertaining to ATMPs manufacture Good Manufacturing Practice and Good Clinical Practice Thorough understanding of gene and cell-based therapies Thorough understanding of HTA Proven experience … team Experience of using Q-Pulse Skills/Abilities Essential Writing and presentation of reports using computers Training and supervision of staff Personnel management Good organisational and leadership skills Strong communication skills (verbal and written) Strong problem-solving skills Ability to work independently and as part of a team … Good attention to detail and accuracy Desirable Project management Disclosure and Barring Service Check This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly 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 »

Proclinical is seeking a dedicated and experienced Senior GCP Quality Auditor. This role is an integral part of the growing global team, contributing to the development and enhancement of audit strategy. The successful candidate will be responsible for conducting and managing audit activities in line with regulatory requirements and company … processes/procedures. Skills and Requirements: Bachelor's degree in a scientific or health-related field. Lead auditor qualification/certification. Experience in conducting GCP audits. Knowledge of regulatory inspections related to GCP is advantageous. Ability to work independently without supervision. Interested or know someone who might be? Reach out more »

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 »

Job summary Job title - Clinical Trials Pharmacist An exciting opportunity has arisen for two enthusiastic and self-motivated pharmacists to join the Pharmacy Clinical Trials Team as band 7 Clinical Trials Pharmacists. The post holders will be members of the pharmacy clinical trials team at the … the Pharmacy Clinical Trials service in accordance with current UK Clinical Trials Regulations and all amendments, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) guidelines and department procedures, ensuring the provision of a high-quality service to … of practice Desirable Knowledge of basic IMP management Knowledge of clinical trial legislation Knowledge of different phases of clinical trials Undertaken GCP training Other Essential Ability to participate in clinical trial late duty, weekend and on-call rotas and work bank holidays Personal qualities and attributes more »

research organisations (CROs), staff an patients in accordance with current UK Clinical Trials Regulations and all amendments, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), Good Distribution Practice (GDP) guidelines and department procedures. The postholder will support the pharmacy set-up, maintenance … the following: To maintain and support the Pharmacy Clinical Trials service in accordance with current UK Clinical Trials Regulations and all updates, GCP, GMP, GDP guidelines and departmental procedures Performing the operational set-up of all new clinical trials. Day-to-day IMP management activities including shipment … qualifications, in respect of English, an IELTS level of 7 in each component or equivalent Desirable Current certified Good Clinical Practice (GCP) training Experience Essential Demonstrable post-qualification hospital experience including dispensary services and aseptic manufacture Desirable Clinical Trials experience Skills and aptitudes Essential Ability to more »

forward thinking team, working in the centre of London opposite the Houses of Parliament? We are looking to recruit a qualified Cardiac Physiologist/Clinical Scientist, preferably, with BHRS or IBHRE certification in Electrophysiology (EP), however Arrhythmia Specialists with Cardiac Rhythm Management (CRM) accreditation and some EP experience will … Change terms and conditions. Main duties of the job This is a fantastic opportunity for an experienced EP physiologist to expand their knowledge and practice in all arrhythmia types (AF, AT, SVT, VE and VTs) on multiple 3D mapping systems including CARTO, Ensite X and occasionally Rhythmia, plus perform … of only 5 academic health science centres within the UK, in which physiologists are fully integrated. At Guys and St Thomas' we strongly Promote Good Clinical Practice and Quality Assurance, and this is endorsed by supporting staff through the HCPC equivalence process, as well as the HSST more »

in advanced therapies and this role will be required to lead and develop services to respond to the building body of work across new clinical trials and into licensed therapies. The manufacturing facilities at GOSH will be developing into new facilities and you will be key in developing and … of GMP across the MHRA-licensed pharmacy production service, the delivery of GDP in the MHRA-licensed pharmacy distribution service and the delivery of GCP related to pharmaceutical aspects of clinical trials. Working closely with the team in Gene and Cell Therapy this role will be part of a … reporting Horizon scanning Previous experience of clinical audit Ability to take initiative and lead on projects including change management Applications for Research grant GCP Experience of electronic hospital systems Skills and Abilities Essential Good organisation skills/time management Excellent priorisation skills Self Motivated Good interpersonal skills more »

Neurosurgery (NHNN), Queen Square. The holder of this post will rotate through various firms. The post holder will have the same educational opportunities and clinical and educational supervision arrangements as the other neurology/stroke SpRs with NTNs. This position is for 6 months starting in August 2024. Main … duties of the job The Trust Grade Doctor will have primary charge of the day to day care of Neurology/Stroke inpatients. Clinical duties will include attending consultant ward rounds, attending outpatient clinics and mdt meetings. The post holder will provide neurological assessment and clerking at admission and … care, imaging, nuclear medicine and pathology. We are committed to sustainability and have pledged to become a carbon net zero health service, embedding sustainable practice throughout UCLH. We have set an ambitious target of net zero for our direct emissions by 2031 and indirect emissions by 2040. Job description 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 »