Senior IRT Systems Design Project Lead

IQVIA LLC; Basel; Vor Ort; CHF 120.000 - 160.000; Vollzeit

Zusammenfassung

IQVIA LLC seeks a Systems Design Project Manager for IRT Basil, Switzerland, to design and deliver IRT systems for clinical trials. You will work with sponsors to translate study requirements into system specs, oversee implementation, and manage timelines, reporting, and finances.

The role demands substantial IRT experience, strong communication, and the ability to lead cross-functional teams in a regulated environment. Travel and client-facing activities are expected as needed.

Qualifikationen

• Bachelor's degree required.
• Mandatory experience in IRT system design.
• SQL experience desirable.
• Strong communication and interpersonal skills.
• Ability to work independently with minimal direction.
• Proficiency with MS Office and general software tools.

Aufgaben

• Analyse study protocols and define IRT system needs with clients.
• Consult with sponsors on the best approach to IRT system setup and design.
• Author user requirement documents and lead review cycles with internal and external teams.
• Develop and manage project timelines to ensure on-time delivery.
• Prepare project reports including status updates, tracking metrics, and financial summaries.
• Oversee financial elements such as deliverable tracking and invoice approval.
• Coordinate cross-functional teams to ensure alignment and milestone achievement.
• Lead issue resolution and support continuous improvement initiatives.
• Contribute to proposals and RFPs as needed.
• Mentor junior PMs and support team development.
• Present project updates at internal and external meetings.
• Ensure compliance with SOPs, policies, and quality standards.

Kenntnisse

IRT system design

Project management

Client-facing communication

SQL

Independence / self-direction

MS Office

Ausbildung

Bachelor's degree

Tools

MS Office

Jobbeschreibung

IQVIA LLC seeks a Systems Design Project Manager for IRT Basil, Switzerland, to design and deliver IRT systems for clinical trials. You will work with sponsors to translate study requirements into system specs, oversee implementation, and manage timelines, reporting, and finances.

The role demands substantial IRT experience, strong communication, and the ability to lead cross-functional teams in a regulated environment. Travel and client-facing activities are expected as needed.