Clinical Data Manager in England

SciPro are partnered with an exciting client who's mission is to detect cancer quickly and accurately using machine learning (ML) and artificial intelligence (AI) techniques alongside MRI scans.

Their goal is to create precise, accessible, cost-effective, and efficient cancer screening.

They're assembling a team of skilled individuals specializing in Artificial Intelligence, UI, and medical imaging to achieve this objective.

We are looking for a clinical data management professional to join their diverse team.

The main focus of this role involves coordinating clinical research projects and ensuring the collection of precise and reliable data sets from external providers and our NHS and partner sites.

The perfect candidate should have a solid grasp of clinical research, clinical data management principles, regulatory guidelines, and industry standards.

You should be ready to work autonomously and cooperatively with diverse teams to guarantee the punctual and precise delivery of data from our NHS sites and partners.

Your skills 3+ years' experience in clinical data management or similar roles in pharmaceutical/clinical researchStrong understanding of clinical trial processes, GCP, and regulatory guidelinesProficient in EDC systems and clinical data management softwareFamiliarity with NHS regulatory framework and approvals processesExperience with SOPs and handling personal identifiable dataSkilled in writing data management plans and other relevant documentsAttention to detail, problem-solving, and analytical skillsExcellent organizational and time management abilitiesTeam player with a flexible approach and willingness to learnYour roleProject manage data acquisition for regulatory submissions and publicationsCreate and maintain external study-level dataset specificationsLiaise with external dataset providers and manage dataset transfersConduct technical checks on received data for complianceCoordinate data workflow and annotation projectsDevelop and maintain data management documentationConfigure and manage EDC systems, conduct user acceptance testing, and train research sitesSet up processes for managing clinical imaging datasetsCoordinate research studies with healthcare partners and ensure timely dataset deliveryPerform data cleaning activities and implement quality control measuresDevelop and execute data management SOPs or trial specific instructionsGenerate and review data listings, summaries, and reports for clinical study reportsAct as the main point of contact for research sites, providing ongoing support and feedbackMonitor study progress and draft regular reportsExport data for analysis in accordance with data management plans