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Job Post Details

Central Monitor/Sr. Central Monitor (Remote) - job post

3.7 out of 5
Desde casa
Tiempo completo
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Información del empleo

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Tipo de empleo

  • Tiempo completo


Desde casa

Descripción completa del empleo

Job Overview

A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts.

Essential Functions:

  • Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs, respective regulations and guideline.

  • Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.

  • Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).

  • May assist in developing required basic data analytics scope and performing the trend analytics for their respective study(ies).

  • Participate on study team meetings and interact with cross functional staff to verify information and/or triage new data issues or prior identified action items.

  • Escalate quality issues pertaining to site to respective Centralized Monitoring Lead/ Sr. Central Monitor.

  • May perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review.

  • Interaction with sites/CRA and follow-up on study required milestones from the project start until close out.

  • May act as backup/ perform the activities as per the task list delegated by Central Monitor Expert/Centralized Monitoring Lead.


  • Bachelor's degree in life sciences or related field, or nursing qualification; or be near to obtain the degree.

  • At least 2 years of relevant clinical research experience.

  • Excellent written and verbal communication skills, good command of English language (mandatory).

  • Experience in monitoring (on site or remote) or previous experience as a study coordinator.

  • Advanced level of Excel.

#LI-Remote #LI-NRJ

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

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