Clinical Data Manager II / Senior Clinical Data Manager

P
Precision for MedicineClinical Trial Services
We can consider candidates based in the UK, Poland, Hungary, Romania, Serbia or Slovakia.Full-TimeSenior
Salary not disclosed
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Job Details

Languages
English
Experience
8+ years’ experience as a Sr. Clinical Data Manager or 5+ Years as a Clinical Data Manager II
Required Skills
Microsoft Office

Requirements

  • 8+ years of experience as a Sr. Clinical Data Manager or 5+ years as a Clinical Data Manager II.
  • Experience working for a Clinical Research Organization, pharmaceutical, or biotech company.
  • Demonstrated experience in database setup and database migrations.
  • Proficiency in Microsoft Office suite (Word, Excel, PowerPoint, Outlook).
  • Professional proficiency in the English language, both written and oral.
  • Experience utilizing various clinical database management systems.
  • Broad knowledge of drug, device, and/or biologic development processes.
  • Strong organizational, leadership, and interpersonal skills.
  • Oncology experience is preferred.
  • Ability to undertake occasional travel as required.

Responsibilities

  • Serve as the primary Data Management contact (Lead DM) for assigned clinical projects.
  • Oversee the project data entry process, including guidelines and quality control.
  • Develop CRF specifications from study protocols and coordinate stakeholder feedback.
  • Conduct database build UAT and maintain quality-controlled documentation.
  • Train clinical research personnel on study-specific CRF, EDC, and project items.
  • Review and query clinical trial data according to the Data Management Plan.
  • Liaise with third-party vendors, including external data and EDC providers.
  • Identify and troubleshoot operational issues based on metrics, audit reports, and team input.
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