4 of 4 Good Clinical Practice Jobs in the North West

management plans, data dictionaries, CRF completion guidance, study-specific procedures, templates and other supporting documentation. Coordinate the timely collection, electronic entry and verification of clinical data from participating sites, including data required for regulated post-marketing surveillance studies. Review submitted data for completeness, consistency and accuracy, raising and resolving … Degree in life sciences health sciences data management or a related subject or equivalent relevant professional experience Current Good Clinical Practice GCP training Desirable Relevant postgraduate qualification or formal training in clinical research or data management Physical and other requirements Essential Able and willing to travel ...

Quality: You will apply a sound working knowledge of UK research governance, HRA and Research Ethics Committee requirements, Good Clinical Practice (GCP) and sponsor responsibilities. You will ensure appropriate compliance with UK GDPR, the Data Protection Act 2018 and NHS information-governance requirements, maintaining confidentiality and appropriate … degree in life sciences, health sciences, data management or a related subject, or equivalent relevant professional experience. Current Good Clinical Practice (GCP) training. Substantial experience in clinical research, clinical data management or study coordination. Experience designing and implementing paper or electronic Case Report Forms (CRFs ...

validate the final report. To assist VEU Management in monitoring capability issues. To ensure adequate care, maintenance and security of laboratory premises and equipment. Clinical Governance To participate in audit processes, clinical trials, and research projects, as required. To assist in the management and monitoring of laboratory … Unit maintains United Kingdom Accreditation Service (UKAS) ISO 15189, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP) and Medicines for Health Regulatory Authority (MHRA) GCP for Laboratories. To investigate clinical and non-clinical incidents in relation to the Units laboratory ...

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 ...