Data Management Lead/Senior Clinical Data Science Lead - Client Dedicated

165452
  • Competitive
  • Warsaw, Poland
  • Permanent
Lead Clinical Data Manager
About the role
As a Senior Clinical Data Science Lead/Lead Clinical Data Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


Primary Location: Poland (remote/hybrid)
 
What you will be doing:
  • Lead end to end data review activities performed on a clinical trial as a Lead Data Manager.
  • Oversees the collection of all clinical trial data from multiple sources.
  • Accountable for achieving clinical data science deliverables on-time, with high quality and to agreed financial metrics.
  • Serve as primary point of contact for internal and external team members regarding clinical data review activities and leads these data review activities to ensure delivery of data fit for analysis.
  • Provides input into clinical system development activities and clinical risk management activities.
  • Oversees the collection of all clinical trial data from multiple sources.
  • Performs DM vendor oversight activities across multiple studies. Reviews and gives input in vendor oversight processes.
  • Review Key Risk Indicators (KRIs) outputs in aggregate across sites, regions and countries. As needed, review study level operational and patient data to support the investigation and root cause analysis of observations.
  • Provides training and subject matter expertise to lower-level DM peers. 
  • Collaborate with clinical operations, investigators, and other stakeholders to ensure smooth data flow throughout the trial.



You should have:
  • 8+ years related experience in pharmaceutical, clinical research or health services industry with a minimum of 6 years’ experience as Data Manager with progressive levels of responsibility. 
  • Degree qualified in a relevant Scientific or Healthcare discipline.
  • Good knowledge of clinical data science activities (Data review, risk management & analytics, clinical systems).
  • Very strong subject matter expertise in the Data Management (DM) discipline. Ability to support multiple studies concurrently with little to no oversight by functional manager.
  • Strong computer skills, including database management software, reporting tools, medical coding tools, and solid understanding of Central Monitoring tools etc. 
  • Strong understanding of different types of data sources in a clinical trial setting and/or expertise with external data types. 
  • Engaging, supportive and you lead by example.
amelia koncki Client Associate

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