Centralized Monitor

Zaf Iqvia Rds Clindepharm; Gauteng; On-site; ZAR 865 000 - 1 126 000; Full time

Job summary

A global provider of clinical research services is seeking a Centralized Monitor based in Gauteng, South Africa. The role involves performing monitoring activities, ensuring quality data integrity, and supporting clinical trial conduct across multiple projects. Candidates should have a Bachelor’s degree in life sciences and experience in the clinical research field. This is a full-time position with a focus on problem-solving and data analysis.

Qualifications

• 2 years experience in clinical research field preferred.

Responsibilities

• Perform centralized monitoring activities and evaluate quality and integrity of the study.
• Ensure accurate completion of internal systems and databases.
• Assist in developing data analytics scope and trend analytics.
• Participate in study team meetings and verify information.

Skills

Time management and prioritization

Problem solving

Data analysis

Communication across cultures

Education

Bachelor's degree in life sciences or related field

Job description

Centralized Monitor - Office Based

Provide support to US sites.

Working hours: 13:00

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 Centralized Monitor that we are looking for!

What is a Centralized Monitor

A Centralized Monitor (CM) is a key skilled and clinically experienced team member of IQVIA Centralized 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.

Responsibilities of a CM

• Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol SOPs, respective regulations and guidelines.
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools and reports for project-specific information.
• Manage triggers and prepare i-site pack for respective sites and countries for assigned study(ies).
• Assist in developing required basic data analytics scope and performing the trend analytics for respective study(ies).
• Participate in study team meetings and interact with cross-functional staff to verify information, triage new data issues or prior identified action items.
• Escalate quality issues pertaining to site to the respective Centralized Monitoring Lead / Sr.
• Perform subject-level data review that requires further investigation with the clinical site to determine overall accuracy.
• Review any other information as necessary to determine overall readiness of the patient information for next-level review.
• Interact with sites / CRAs and follow‑up on study‑required milestones from project start until close‑out.

Qualifications

• Must have a Bachelors degree in life sciences or related field.
• 2 years experience in clinical research field preferred.

About IQVIA

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.

Employment Details

Employment Type: Full‑time.

Vacancy: 1.