Oil & Gas Ot Maintenance Engineer – Scada/Plc/Cyber

NeoWork; Buenos Aires; On-site; ARS 600,000 - 800,000; Full time

Job summary

IQVIA in Buenos Aires, Argentina, is seeking a Maintenance Associate to support study delivery during the maintenance phase of clinical trials. You will work closely with Maintenance Leads and CTRMs to ensure maintenance and regulatory activities are executed accurately and on time.

Responsibilities include maintaining internal systems, dashboards, and documentation; coordinating with cross-functional teams to meet timelines and budgets; and proactively identifying risks using data to safeguard

Qualifications

• Bachelor's Degree in Life Science or related field.
• Minimum 2 years' work experience; healthcare preferred.

Responsibilities

• Support study maintenance and regulatory activities across assigned studies.
• Coordinate with maintenance leads and CTRMs to meet timelines and budgets.
• Maintain dashboards and data to monitor study performance and compliance.

Education

Bachelor's Degree in Life Science or related field

Job description

Buenos Aires, Argentina
Mexico City, Mexico
São Paulo, Brazil
Bogota, Colombia
Full time
R
**Maintenance Associate - Country Site Activation**
**Make an impact on patient health!**
IQVIA's Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; 'Always Impatient for the Patient' and we excel in our collaboration with our external/internal customers. IQVIA's Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.
**Summary:**
As a **Maintenance Associate** , you will play a key role in supporting study delivery during the maintenance phase of clinical studies. Working closely with Maintenance Leads and Clinical Trial & Relationship Managers (CTRMs), you will help ensure the successful completion of all required maintenance and regulatory activities across assigned studies or multi‑protocol programs.
You will be responsible for understanding the scope of work, budgets, and resource requirements, and for ensuring study activities are executed accurately and efficiently.
**Key Responsibilities**

• Support the setup, updating, and ongoing maintenance of internal systems, databases, tracking tools, timelines, and project plans with complete and accurate study‑specific information.
• Collaborate with cross‑functional stakeholders to ensure maintenance and regulatory activities are completed in line with timelines, budgets, and compliance requirements.
• Manage, utilize, and interpret various study dashboards to analyze data, monitor study metrics, and track compliance.
• Proactively identify risks, issues, and trends through data analysis and elevate appropriately.

**Requirements:**

• Bachelor's Degree in Life Science or related field
• Minimum 2 years' work experience; preferably in in healthcare or similar