Hybrid Lab Projects Coordinator for PM Support & Monitoring

IQVIA

Livingston

Hybrid

GBP 27,000 - 37,000

Full time

4 days ago
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Benefits offered by this job

Global exposure
Therapeutic area variety
Collaborative team environment
In-house technology access
Career development opportunities
Work-life balance

Job summary

IQVIA Laboratories is seeking a Project Coordinator for Project Services to join our Livingston team on a hybrid basis, with one day per week at the Livingston office. You will support the Project Manager by preparing minutes, action logs, and protocol-specific documents, while assisting with Laboratory Centralized Monitoring tasks across studies.

The role requires a life sciences degree and 1+ years in clinical/healthcare, with strong communication, problem‑solving, and multitasking abilities.

Qualifications

  • Bachelor's degree in Life Sciences or related field.
  • 1+ years relevant experience in clinical/healthcare environment preferred.
  • Strong written and verbal communication skills in English.
  • Ability to manage competing priorities and work in a fast-paced setting.

Responsibilities

  • Attend meetings and prepare minutes and action logs.
  • Oversee setup of protocol-specific Laboratory Centralized Monitoring requirements under supervision.
  • Handle site loading, Investigator Portal access, kit shipments, and day-to-day study monitoring.
  • Coordinate with internal and external teams to resolve queries and escalations.
  • Lead customer communications during manager absence and support project close-out.

Skills

Communication
Problem solving
Multi-tasking
English proficiency
Teamwork
Office software

Education

Bachelor's degree life sciences

Tools

Microsoft Word
Microsoft PowerPoint
Microsoft Excel

Job description

IQVIA Laboratories is seeking a Project Coordinator for Project Services to join our Livingston team on a hybrid basis, with one day per week at the Livingston office. You will support the Project Manager by preparing minutes, action logs, and protocol-specific documents, while assisting with Laboratory Centralized Monitoring tasks across studies.

The role requires a life sciences degree and 1+ years in clinical/healthcare, with strong communication, problem‑solving, and multitasking abilities.

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