Join us on our exciting journey!
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
Are you :
Someone who understands dynamics of working with the sites?
Results driven and detail-oriented?
Good at supporting others on problem solving?
Good at planning, time management and prioritization?
Skilled at software and computer use, that enjoys technology applied to data analysis?
Understands clinical trial conduct, and skill in applying applicable clinical research regulatory requirements and relevant local laws, regulations and guidelines?
Able to communicate efficiently and work well across cultures and geographies?
If you have answered yes’ to any of the above questions, you might be the Central Monitor that we are looking for!
What is a Central Monitor?
A Central Monitor (CM) is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. A CM provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts.
What are the responsibilities of a CM?
As a CM, you will :
Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs respective regulation and guidelines.
Ensure accurate completion and maintenance of internal systems, databases, tracking tools / reports for the project specific information.
May perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned studies.
May assist in Developing required basic data analytics scope and performing the trend analytics for their respective studies.
May participate in (study) team meetings and interaction 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.