IQVIA
Life Sciences
AssociateCentralizedMonitor
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Associate Centralized Monitor at IQVIA. Skills: Centralized Monitoring, Site Performance, Risk Management. Provide project related assistance. Ensure work conducted in accordance with SOPs”
What You'll Achieve.
Meeting quality metrics; Meeting timeline metrics
Industry & Context.
Root cause analysis
What They're Looking For.
Must Have
2 years of work experience, 6 months relevant experience, Basic knowledge of applicable research and regulatory requirements, Exposure to Microsoft Applications, Effective written and verbal communication skills, Effective time management skills, Ability to establish and maintain effective working relationships, Good data entry skills
Nice to Have
Sc Degree in Life Sciences or educational equivalent
What You'll Do.
Provide project related assistance
Ensure work conducted in accordance with SOPs
Meet quality and timeline metrics
Complete role-specific training
Provide study level administrative support
Prepare status reports
Create study trackers
Maintain study trackers
Follow up for outstanding issues
Assist in updating systems
Assist in maintaining systems
Drive tracking compliance
Perform delegated tasks
Assist in preparation of i-site pack
Pull associated reports
Perform access management tasks
Process access requests
Follow up with vendors
Support technical solution specialist
Periodic review of site level KRIs
Periodic review of historic site performance
Facilitate early identification of site-level risk
Facilitate early identification of site-level issue
Monitor site performance
Make recommendations for corrective actions
Review effectiveness of recommended actions
Take appropriate additional actions
Review Study Central Monitoring Plan
Attend Kick-Off meetings
Attend weekly team meetings
Attend client meetings
Adhere to key activities outlined in SOW
How You'll Work.
Team & Collaboration
Clinical study management team; CMS leads; Technical solution specialist; Client meetings
Communication Scope
Written communication; Verbal communication; English language
Full Job Description
**_Job Overview_** Provide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics. **_Essential Functions_** * Complete appropriate role-specific training to perform job duties.; * Under supervision, provides study level administrative support to the clinical study management team (examples of such tasks include, but not limited to running system reports, preparing and distributing status reports, creating and maintaining study trackers, follow-up for outstanding issues, etc.).; * Under supervision, assist in updating and maintaining systems within project timelines/plans and driving tracking compliance in various systems to enable credible data for analysis.; * Perform the activities as per the task list delegated by CMS leads.; * Assist CMs in the preparation of i-site pack for their respective sites and countries for assigned studies, by pulling associated reports.; * Perform assigned access management related administrative tasks to support team members with project execution, example of tasks includes, but not limited to processing access requests, following up with relevant vendors, etc.; * Provide support to technical solution specialist (TSS) on formulations in Excel and on the front-end part.; * Periodic review of site level KRIs and historic site performance according to Central Monitoring Plan * Facilitating 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 (eg Site Telephone Contact or Triggered Onsite Monitoring Visit) * Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed * Review of the Study Central Monitoring Plan * Attend Kick-Off meetings, weekl
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