4 of 4 Permanent Good Clinical Practice Jobs in Manchester

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 ...

Senior Clinical Data … Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.Summary of the Essential Functions ...

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 ...