Clinical Quality Manager (R1107350) - Singapore, SG - IQVIA™

Date de publication 2/29/2020

Résumé de l'offre

  • Type d'employé
    CDI / CNE
  • Expérience
    Not Specified
  • Date de publication
  • Job ID:

Description de l'offre

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.


  • Adopt and implement the Global Quality Management Plan within the scope of the assignment; this will include: planning and executing the Quality Management activities; risk identification and evaluation through quality assessments either remote or on site; providing support in risk mitigation, in planning corrective/preventive actions and guidance for improvement; supporting the RWAS line management and staff to enhance effectiveness of procedures and quality practices
  • Cooperate closely with the relevant Heads of business and other stakeholders, support maintaining focus on quality in project delivery. Contribute to the development and implementation of project- or Sponsor-specific Quality Managements and Risk Management Programs; monitor the implementation and delivery
  • Provide advice and support to operational teams and functional departments including key stakeholders on GxP compliance
  • Work in close cooperation with operational teams to manage non-compliance, quality issues; assist in planning corrective/preventive actions, as applicable according to SOPs
  • Inform Heads of Quality Management, Heads of the assigned business line and Quality Assurance of quality issues according to SOPs
  • Provide assistance to the operational teams in preparing for, and potentially during, audits and regulatory inspections
  • Coordinate with Quality Assurance on clinical quality matters as needed
  • Prepare periodic reports to various levels of the organization on quality related matters, risk assessments and specific quality improvement initiatives


  • Bachelor's Degree in Life Sciences or Nursing qualification
  • Minimum of 4 years’ experience in a Pharma or Clinical-related environment
  • Fluent in written and verbal English communication
  • 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

  • Good organizational, interpersonal and communication skills

  • Good judgement and decision-making skills

  • Strong influencing and negotiation skills

  • Strong computer skills including Microsoft Office

  • Demonstrated ability to work in a matrix environment

  • Excellent problem-solving skills

  • Ability to travel within the region/country if needed

  • Ability to lead and motivate a project or functional team

  • Ability to establish and maintain effective working relationships with co-workers, managers and supported team members

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: R1107350