Clinical Data Manager

1 month ago

United Kingdom SciPro Full time

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. 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.

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
Excellent organizational and time management abilities
Team player with a flexible approach and willingness to learnYour role

Project manage data acquisition for regulatory submissions and publications
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
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
Export data for analysis in accordance with data management plans

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