Clinical Data Manager
£45000 - £50000 per annum
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 research
  • Strong understanding of clinical trial processes, GCP, and regulatory guidelines
  • Proficient in EDC systems and clinical data management software
  • Familiarity with NHS regulatory framework and approvals processes
  • Experience with SOPs and handling personal identifiable data
  • Skilled in writing data management plans and other relevant documents
  • Attention to detail, problem-solving, and analytical skills
  • Excellent organizational and time management abilities
  • Team player with a flexible approach and willingness to learn

Your role

  • Project manage data acquisition for regulatory submissions and publications
  • Create and maintain external study-level dataset specifications
  • Liaise with external dataset providers and manage dataset transfers
  • Conduct technical checks on received data for compliance
  • Coordinate data workflow and annotation projects
  • Develop and maintain data management documentation
  • Configure and manage EDC systems, conduct user acceptance testing, and train research sites
  • Set up processes for managing clinical imaging datasets
  • Coordinate research studies with healthcare partners and ensure timely dataset delivery
  • Perform data cleaning activities and implement quality control measures
  • Develop and execute data management SOPs or trial specific instructions
  • Generate and review data listings, summaries, and reports for clinical study reports
  • Act as the main point of contact for research sites, providing ongoing support and feedback
  • Monitor study progress and draft regular reports
  • Export data for analysis in accordance with data management plans
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