Centralized Monitoring Lead (R1118965) in Beijing, China at IQVIA™

Date Posted: 3/25/2020

Job Snapshot

  • Employee Type:
    Full-Time
  • Experience:
    Not Specified
  • Date Posted:
    3/25/2020
  • Job ID:
    R1118965

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.

• Provide oversight on clinical deliverables on assigned projects as per the protocol, SOPs, respective
regulation/guidelines and project Clinical Operation Plan (COP) from Applications/ Analytics/ Therapeutics/
Quality perspective.
• Perform functional lead responsibilities for assigned project deliverables for specific customers or
projects/specified.
• Independently manage assigned studies.
• Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
• Contribute and/or oversee to the development and use of study management plans, specific tools and
document templates and/or other study specific plans to evaluate the quality and integrity of the study;
including complete and accurate documentation so that the project is audit ready.
• Support project management team to develop monitoring strategy including monitoring triggers/thresholds.
• Manage and monitor operational insight of the assigned project(s) and complete/oversee the study/site
metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review,
triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.).
• Contribute to developing the study specific analytics strategy and work on developing advanced analytics.
• Provide Inputs to clinical study teams, key decision makers, and internal team members to manage
continuous process improvements, issue escalation, workload projections
• Identify the value adds from the medical review & remote monitoring in the study and provide the inputs to
relevant stakeholders.
• Manage project resources (CRAs/ /CTAs/Centralized monitoring team)
• Oversee the IP management for the assigned study to identify risk and proposed mitigation (including resupply,
re-labelling, Import/export licenses etc.).
• Take up customer lead activities to provides oversight of unblinded monitoring procedures on a study.
• Act as mentor or coach for junior CMS staff.
• Support the Centralized Monitoring Advisor/Centralized Monitoring Manager in periodic review of Centralized
monitoring trainings and/or identify the training needs of the team and provide inputs whenever required.
• Conduct periodic review of site level KRIs and historic site performance according to Central Monitoring Plan
• Early identification of site-level risk/issue(s) occurring during study conduct and responsible for identification
of risk
• Monitor site performance and make recommendations for timely corrective actions (e.g. Site Telephone
Contact or Triggered Onsite Monitoring Visit)

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: R1118965