Central Monitor (Centurion or Cape Town based) - (1807648) in Centurion, ZA at IQVIA™

Date Posted: 6/7/2018

Job Snapshot

Job Description

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. 

Job Requirements

You must have a Bachelor's degree in life sciences or related field, or nursing qualification; or be near to obtaining the degree.

At least 2 years of relevant clinical research experience.

Why should you apply?

You will be part of a dynamic new group with many growth opportunities.

You are going to be doing clinical research differently in an exciting, pioneering way.

You do not need to travel on a regular basis.

There is a possibility of working from home with flexible hours.

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.

Job ID: 1807648