Clinical Data Management Development Professional

Há 6 dias


Lisboa, Lisboa, Portugal IQVIA Tempo inteiro

Job Summary

We are seeking an experienced Clinical Data Management Development Professional to join our team at IQVIA. As a key member of the Real World Evidence Data Management department, you will be responsible for developing and maintaining training plans, facilitating quarterly or annual reviews, and creating training slides and materials.

Key Responsibilities

  • Collaborate with Subject Matter Experts to develop and maintain Training Plan requirements and roles
  • Facilitate quarterly or annual training plan reviews
  • Develop training slides and material independently or with Subject Matter Experts
  • Plan, coordinate, and communicate the training schedule for the Real World Evidence Data Management department
  • Perform training courses as needed and agreed with other stakeholders
  • Provide oversight of training delivered by other stakeholders
  • Monitor effectiveness and timeliness of training

Training Content

  • Set up and maintain folder on Data Management SharePoint site
  • Update/archive training items in alignment with Training Plan updates

Training Compliance

  • Plan and support development of Compliance Reports
  • Provide review and/or oversight of staff onboarding training compliance
  • Provide review and/or oversight of monthly/quarterly training compliance data
  • Collaborate with Managers to ensure adherence to training compliance targets

Other Initiatives

  • Participate, support, or lead global initiatives to continuously improve training processes or compliance across Real World Evidence Data Management
  • Provide input on Data Management process improvements
  • Provide input on the development and implementation of a new technology or tool
  • Participate in focus teams and global or local best practice teams as relevant

Requirements

  • Sound working knowledge of clinical data management procedures, ICH-GCP, applicable regulatory requirements, medical terminology, and quality management processes
  • Knowledge of Drug Development processes
  • Knowledge of CRO or Pharmaceutical Industry operations
  • Sound knowledge of current training practices
  • Good organizational, interpersonal, and communication skills
  • Good judgment and decision-making skills
  • Strong influencing and negotiation skills
  • Strong computer skills including Microsoft Office and Data Management applications including EDC (Medidata Rave)
  • Demonstrated ability to work in a matrix environment
  • Excellent problem-solving skills
  • Ability to travel within the region/country
  • Ability to lead and motivate a training team
  • Ability to establish and maintain effective working relationships with co-workers, managers, and clients/customers

Salary

The estimated salary for this position is $120,000 - $150,000 per year, depending on experience.

About Us

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at iqvia.com.



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