Study Data Lead (Clinical Data Management) | SwiconJobs

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Study Data Lead (Clinical Data Management)

2021.12.07. | Budapest | Non-tech
Introduction
Our partner, one of the largest ICT consulting conglomerates, solves great challenges through the power of digital technology for various industries. Their dynamic expansion is realized through dedication to customer service and industry expertise with more than 450.000 employees around the world.
Tasks
  • General responsibility for the data management activities for studies, including the study set up, conduct and close out
  • Providing support and training on the clinical data management activities to data managers for the relevant functional processes, work statements and projects
  • Maintaining & building awareness of internal and external clinical data management practices to enhance domain expertise 
  • Liaising with the client's study data manager and designee
  • Monitor and evaluate overall study progress, identify the potential risk / challenges faced during the course of the study 
  • Conduct regular team meetings for study updates and provide guidance on study related issues to client as well internal teams 
  • Monitor, maintain & report KPI / SLAs /metrics on the study 
  • Ensure adequate resource for the study throughout its lifecycle in collaboration with group leader and inform client contact of any changes in staff 
  • Keep the Group Lead & Project Manager fully informed about the need for the resources so the resource requests can be finalized with client AM and PM 
  • Set priorities and targets of the study within the CP, DM, CCS, DAS teams 
  • Responsible for recruitment, selection, training of team members & managing attrition
Expectations
  • Experience in Clinical Data Management 
  • Good knowledge of MS Office 
  • Excellent technical skills, start-up knowledge 
  • Excellent verbal and written communication skills
  • Good organizational, interpersonal and team skills 
  • Project management skills 
  • Strong knowledge of Good Clinical Practices, Good Manufacturing Practices, Clinical research, Clinical trial process and related regulatory requirements and terminology
  • Ability to work across scientific and technical disciplines
Advantageous
  • Knowledge of PL/SQL
Employer's offer
  • A great diversity of cultures 
  • Language courses and training 
  • On-site relax & gym rooms 
  • Volunteering, sport and employee events