5 of 5 Good Clinical Practice Jobs in Oxfordshire

at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking an Associate Director, Clinical Data Management who can lead and oversee end to end Clinical Data Management activities on assigned studies and programs. You’ll also play a critical role in the … be responsible for leading and delivering initiatives for CDM within the Biometrics group. You’ll also be proactive and be keen to collaborate with cross functional groups within the Clinical Development organization and larger Data Science teams at Recursion. Daily, you will be responsible for all the CDM study activities and deliverables, document reviews, oversight of CRO’s, timelines … ability to manage outsourced studies and lead DM and external vendor oversight activities and deliverables.Proficiency in project management leading 3-4 outsourced programs, simultaneously. Represent Data Management function in Clinical Study Meetings, ensuring proactive alignment of expectations between the CRO and Recursion regarding all data-related deliverables. Work with CRO and Recursion functional groups to complete EDC set up More ❯

Fixed-term for 3 years in the first instance Hours: Full time About the role We have an exciting opportunity for a Senior Data Manager to join the Oncology Clinical Trials Office (OCTO). OCTO, part of the University of Oxford's Department of Oncology, is a leader in early cancer detection, precision prevention and therapy trials, delivering groundbreaking … clinical research. As the Senior Data Manager, you will be responsible for ensuring that data collection systems and data management activities are appropriately designed, implemented, maintained, or developed to support the collection of high-quality clinical trial data sets for analysis, publication, and, where appropriate, future data sharing. Data from multiple sources needs to be integrated in an … data management and information governance within clinical trials, including CTIMPs, in a sponsor organisation. You will have experience of implementing approaches to ensure compliance with high standards of GCP, the requirements of UK clinical trials and data protection legislation, and will have experience of developing and delivering training in relation to data management and integrity. You will have More ❯

providing aseptically prepared clinical trial doses for patients across different specialities within the Trust and maintaining up-to-date documentation according to Good Clinical Practice (GCP). The main role of this post is to supervise and manage the day-to-day service provided by CTASU and to ensure that aseptic preparation of medicines is run … working knowledge of the Medicines for Human Use (Clinical Trials) Regulation (EU Directive 2001/20EC), Human Medicines (EU Exit) Regulations 2019 and the International Conference on Harmonisation GCP Guideline (ICH GCP), as applicable to the dispensing of Investigational Medicinal Products for clinical trials or other products e.g. NIMPs, physiological compounds given to study subjects. To facilitate NHS … competency frameworks where appropriate. Clinical Trials To ensure all CTASU staff are in compliance with relevant standards for the operation and management of Clinical Trials, including ICH-GCP and GMP. To ensure all members of the CTASU staff have appropriate ICH-GCP training. To work within the Medicines for Human Use (Clinical Trial) Regulations 2004 and EU More ❯

talk with your recruiter to learn more. Base pay range Product Manager - Health Tech Company Join Us in Revolutionising Healthcare! Are you passionate about leveraging technology for the greater good? Here's your chance to make a tangible impact on global health! This cutting-edge Health Tech Company is at the forefront of innovation. Be part of the journey … years of product management experience in healthcare technology Working knowledge of healthcare data standards, particularly FHIR Product analytics, UI/UX feedback loops, and process optimization Experience with clinical workflows and healthcare IT systems Strong analytical and problem-solving skills Excellent communication and stakeholder management abilities Bachelors degree in a relevant field Previous product management training (Pragmatic Marketing, Design … etc.) Preferred Experience in API-based data exchange, data mapping, and validation rules Experience with clinical research or EDC systems Knowledge of regulatory requirements for clinical trials (GCP, 21 CFR Part 11) Familiarity with Agile development methodologies What's On Offer Competitive Salary and Benefits: We value our team and offer a competitive compensation package. Cutting-Edge Technology More ❯

and Laboratory Buyer to join our team and source, negotiate, purchase and manage the supply of essential materials and equipment for the facilities department, including both laboratory research and clinical operations. This role involves working closely with the Head of Procurement to ensure that the right equipment is acquired with cost, time efficiency and in compliance with all regulatory … standards. This role offers the opportunity to work in a highly collaborative, fast-paced environment, supporting cutting-edge research whilst playing a critical role in ensuring that laboratory and clinical teams have access to the resources they need for successful project execution. Key Responsibilities: Sourcing & Procurement: Identify, evaluate, and procure high-quality lab and clinical equipment. Obtain quotes … Experience working with laboratory reagents, consumables, equipment, and clinical trial supplies is highly preferred. Knowledge of Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and regulatory requirements related to procurement in scientific settings. Desirable Skills, Qualifications & Experience: Experience with procurement software, ERP systems, and inventory management tools is desirable. Educated to MSc or equivalent More ❯