4 of 4 Good Clinical Practice Jobs in the Thames Valley

Function: Data Analytics & Computational Sciences Job Sub Function: Biostatistics Job Category: People Leader All Job Posting Locations: High Wycombe, Buckinghamshire, United Kingdom Job Description: We are recruiting for a Clinical Programming Portfolio Lead for our location in High Wycombe The Clinical Programming Portfolio Lead is a highly experienced individual with expert understanding of programming strategies, practices, methods, processes … and contribute to organizational effectiveness, transparency, and communication. Directly contributes to delivery of the J&J IM R&D portfolio through effective leadership and accountability of large or complex clinical development and strategic innovation of programs and projects. In collaboration with Senior departmental leadership, the Clinical Programming Portfolio Lead influences departmental effectiveness acting as a change agent to … years of experience in Pharmaceutical, CRO or Biotech industry or related field or industry. In-depth knowledge of programming practices (including tools and processes) and regulatory guidelines (e.g., ICH-GCP) Project, risk, and team management and an established track record leading teams to successful outcomes. Established track record collaborating with multi-functional teams in a matrix environment and partnering with More ❯

IDAR) organization. The Principal Engineer Digital Health Enablement is responsible for shaping the interfaces between partners, system and process for capabilities administered by Enabling Analytics & System Excellence EASE within Clinical Trial Management Solutions (CTM Solutions) or Investigator & Patient Solutions (I&PS). • The Principal Engineer Digital Health Enablement within CTM Solutions will oversee end to end system planning, administration … oversight and related processes for capabilities supporting clinical trial document management/TMF, study management and oversight. • The Principal Engineer Digital Health Enablement will oversee end to end system planning, administration, oversight and related processes for capabilities supporting patient engagement, site staff enablement, clinical staff training. This includes driving customer enablement and innovative solutions for the supported capabilities … leading inspection-ready practices for the supported capabilities, with a focus on delivering measurable value for stakeholders. • Lead change management efforts, promoting the adoption of new tools and ensuring clinical trial teams are well-equipped to use them effectively. • Remaining connected as a primary point of contact with stakeholders, functional area points of contact and subject matter expert frameworks. 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 ❯

eSOURCE Data Acquisition Expertise. The Data Acquisition Expert 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. Activities are conducted in close collaboration with Data Managers, Study Responsible Physicians (SRP) and Study Responsible Scientists (SRS) . External data streams … and sensors and other digital data collection technologies. Base Level: Bachelor's degree or equivalent, preferably in Computer Science. Minimum of 3 years' experience managing data in support of clinical research. Experience working with external data e.g., Safety Lab, PK, Simple Biomarkers, ECG … or similar. Experience working on clinical trials. Experience working in highly diverse teams within clinical research; cross-functional, global, multiregional. Working knowledge of SDTM. Working knowledge of GCP/ICH guidelines Excellent written and verbal communication in English. Demonstrated experience in working with external data providers within a clinical study setting. Experience developing data transfer agreements. E More ❯