Offer summary

Qualifications:

Bachelor's degree in life sciences, nursing, or related field, or near completion., At least 2 years of relevant clinical monitoring experience, either on-site or remote., Advanced proficiency in Excel for data analysis and reporting., Fluent in English, with strong communication skills..

Key responsibilities:

Perform centralized monitoring activities to ensure study quality and data integrity.

Manage project-specific systems, databases, and reports.

Interact with study sites and team members to verify data and address issues.

Participate in study meetings and escalate quality concerns as needed.

Job description

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.

Qualifications:

Bachelor's degree in life sciences or related field, or nursing qualification; or be near to obtain the degree.
+2 years of relevant monitoring experience (on site or remote).
Advanced level of Excel.
We are looking for someone with advanced level of English.

This is a home based position.

#LI-Remote #LI-NRJ

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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