10 Good Clinical Practice Jobs in the North West

trials coordination and data management involving clinical trials or project co-ordination, as well as a good understanding of clinical research, GCP and clinical governance. We are looking for individuals with excellent organisation and communication skills, who can work well both in a team and using … support to the senior R&I management and clinical research staff, and ensure compliance with Trust Policy, Good Clinical Practice (GCP) and all other relevant requirements. About us The Christie is one of Europe's leading cancer centres, treating over 60,000 patients a year. We … Research Nurse Team Leader/Research Manager. Person Specification Qualifications Essential Scientific/Business degree or relevant experience in scientific and medical research. Current GCP certification. Desirable Post graduate certificate in clinical research or other relevant post graduate qualification/experience. Management qualification. Experience Essential Line management experience Significant more »

is to support the clinical research team with all aspects of clinical trials administration, according to Good Clinical Practice (GCP), standard operating procedures (SOPs) and Trust policies. The post-holder will be responsible for supporting the delivery of clinical trials within the Clinical … assigned team, under the guidance of the Clinical Research Nurse Team Leader. Maintain investigator site files and essential documentation in accordance with ICH GCP and Trust SOPs to ensure they are always kept inspection ready. Provide administrative support to the Clinical Research Nurses and Principal Investigators for safety … system. Able to assess and interpret clinical/non-clinical information. Knowledge Essential Knowledge of the clinical trials process. Familiar with GCP guidelines/EU directives Desirable Knowledge of issues relevant to paediatric research. Knowledge of patient information systems. Skills Essential Good organisational skills Good more »

provide medical support to the Early Phase Trials team including consultants, nursing and administration staff by primarily acting as co-investigator on early phase clinical trials. The successful applicant will join a highly … motivated and empowered workforce to increase research capacity and deliver innovative early phase research in compliance with Good Clinical Practice (ICH-GCP) and Trust policy. This is a 10 session non-training post funded through The Clatterbridge Cancer Centre for an initial period of 1 year (potential … to extend to 2 years). The Early Phase Clinical Research Fellow role is suitable for individuals towards the end of, or having completed, their specialist oncology training who wish to gain further experience in experimental medicine and Phase I trials, including first-in-human trials, clinical pharmacology more »

Sponsors to provide safe and efficient delivery of studies. Working with the unit teams and medical leads to create and maintain a culture of clinical excellence, process improvement, effective leadership and high standards of volunteer/patient care. KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED: A minimum of 4 years … experience working within a Senior Strategic Management role, along with a good understanding of Clinical Operations. A minimum of 7 years’ experience within the field of clinical trials, Early Phase preferred, or relevant clinical setting RGN/RMN or BSc Nursing/Biomedical or BSc … in a scientific field would be highly desirable RESPONSIBILITIES: Departmental operational oversight of business activities at the Early Phase Unit in accordance with ICH-GCP, MHRA Phase 1 Accreditation, MAC SOPs and Study specific protocols whilst optimising profitability by leading the MAC teams to meet/exceed business projections. Lead more »

Clinical Data Manager – £35,000-£47,000 per annum– Liverpool/Hybrid The Role Do you have a keen eye for detail and a knack for ensuring data accuracy? Are you excited about using cutting-edge AI to transform healthcare? MyCardium AI, a rapidly growing company using AI to … revolutionise cardiac MRI analysis, is seeking a highly motivated Clinical Data Manager to join our team in Liverpool. In this pivotal role, you will oversee the collection, management, and analysis of imaging data from clinical trials. You'll ensure data quality and integrity, working closely with a dynamic … clinical data management, ideally in imaging. Experience with imaging data and software (PACS, DICOM). Knowledge of Good Clinical Practice (GCP) and regulatory guidelines. Proficiency in data management software and databases. Strong understanding of clinical trials and regulations. Excellent organisation and communication skills. Ability to more »

Quality Assurance Manager - Good Clinical Practice Our client, based in Cheshire are recruiting for a contract GCP QA Manager to join them for a 6 month project. This is an exciting opportunity to join a dynamic company with a great culture. Role: Provide strategic direction for quality … CAPA Process to ensure effectiveness Support the development of a risk based audit programme Maintain network of external audit providers to support CMC, pre-clinical and clinical activities. Support the management, implementation, and maintenance of the Quality Management System to support clinical development … activities. Support senior management in providing direction and leadership to staff to ensure a quality mindset is embedded in the business Requirements: Expert in GCP with working knowledge of GMP 5 years experience in a QA Manager role within a CRO, Biotech or Pharma company Contract: Hours: 3 days a more »

Lead Quality Advisor, Clinical Supply Quality Location: UK (Macclesfield) Type: Permanent Competitive Salary & Benefits Be proud to play a significant role to bring safe and effective new medicines to patients. We are adventurous, agile and pragmatic to enable our business to use innovative solutions and technologies to supply clinical trial materials to patients. Business area In the Clinical Supply Quality Team, we are responsible for quality in the development of new Clinical Trials and collaborations and the supply of Investigational Products to them. With a portfolio encompassing both small and large molecules, combination products and ground … and delivery. This may include all Quality aspects of projects including IT projects. Support Clinical Supply functions in GMP inspections and input to GCP inspections where required Approve Clinical Supply GMP documentation Contribute to release and other routine activities required in the clinical supply chain Support quality more »

responsibility for duties including: Designs and oversees the implementation quality management systems for CMC development activities including the release of product for GLP and GCP studies. Provides quality expertise in accordance with the global quality requirements in the creation of product characterisation, product specifications, method validation, stability and comparability assessments … in the collaboration with C(D)MOs. Ensures that there are robust processes in place for the review and release product for GLP and GCP studies. Ensures appropriate quality oversight of GMP activities performed by the Product Development teams at Dechra or CDMOs and contract laboratories. This may include review more »

high quality research and ensure the best use of resources. The post holder will also work closely and collaboratively with senior colleagues within the Clinical Research Division (CRD), in particular the Research Governance Manager and Research Matron to support the effective setup and delivery of studies within the CRF … CRF performance data to determine trends and patterns and collate these data into reports. Responsible for the day-to-day running of the non-clinical aspects of the CRF, including facilities and information management. Taking into account the AHCRF objectives, Trust's overall strategy, Trust research strategy, develop and … Educated to masters level in a subject relevant to the role or equivalent relevant experience. Project management qualification or equivalent relevant experience. Desirable Valid GCP certificate Experience Essential Management within a clinical research environment. Working with clinicians and other health care professionals. Engaging with commercial and academic partners. Experience 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 »