Training Manager, Lifecycle Safety (R1089077) in Dublin, Ireland at IQVIA™

Date Posted: 7/23/2019

Job Snapshot

  • Employee Type:
  • Experience:
    Not Specified
  • Date Posted:
  • Job ID:

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.




The Training Manager, Lifecycle Safety, is primarily responsible for providing training across global Lifecycle Safety functions including ICSR case processing, Regulatory reporting, Medical Information, endpoint adjudication and aggregate reporting. The Training Manager will partner with Lifecycle Safety functional specialists and/or management to assess current training plans and processes looking to identify areas of improvement and delivery across different client projects.


Areas of responsibility include but are not limited to:

  • Project Specific Training Plans:
  • Collaborate with service leads to develop training plan requirements and roles
  • Finalize training plan with agreements from designated IQVIA and Customer contacts
  • Maintain real time ongoing agreements and updates to training plan
  • Facilitate quarterly or annual training plan reviews as required on project
  • Develop training slides and material independently or with service leads or designees
  • Training Content:
  • Set up eTraining folder and confirm role requirements for project
  • Update / withdraw eTraining 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
  • Participate, support or lead development of training plans, material or content for Departmental training needs.
  • Participate, support or lead global initiatives to continuously improve training processes or compliance across LCS and their projects.


  • Sound working knowledge of medical terminology, clinical monitoring procedures (SOPs), ICH-GCP, applicable regulatory requirements, quality management processes
  • Knowledge of National and International Regulations and Drug Development processes
  • Knowledge of CRO or Pharmaceutical industry operations
  • Knowledge of Quintiles corporate standards and SOPs
  • Good organizational, interpersonal and communication skills
  • Good judgement and decision-making skills
  • Strong influencing and negotiation skills
  • Strong computer skills including Microsoft Office and Clinical Trial Management System (CTMS) applications
  • 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 clinical team
  • Ability to establish and maintain effective working relationships with co-workers, managers and clients/customers


  • Bachelor's degree in life sciences or equivalent nursing qualification with a minimum of 6 years’ experience in Lifecycle Safety (Pharmacovigilance, CEVA, Medical Information, Safety Publishing, Risk Management, etc). Preferably with 2 of these years being in a related Training position.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.

Job ID: R1089077