Remote Clinical Study Manager – Oncology Trials Lead

IQVIA; Belgique; Remote; EUR 90,000 - 130,000; Full time

Job summary

IQVIA sponsor-dedicated Clinical Functional Service Partnerships team is seeking a Local Clinical Study Manager to lead and oversee trials across therapeutic areas. The role is full-time and home-based, with location options Belgium/Denmark/Netherlands/Sweden.

You will drive study delivery, manage cross-functional teams, monitor progress, ensure regulatory compliance, and maintain TMF quality, while coordinating with vendors and sites to achieve timelines and quality, in line with ICH-GCP.

Qualifications

• Five or more years in clinical research with at least 2 years in project management.
• Knowledge of international guidelines ICH GCP and local regulations.
• Ability to lead cross-functional teams and drive trial delivery to timelines.

Responsibilities

• Provides overall clinical study leadership and oversight for trial delivery, quality, timelines and outcomes.
• Leads cross-functional teams, sets priorities, and ensures effective communication.
• Plans and oversees daily study monitoring activities and status updates.
• Manages vendors and budgets, and coordinates resources to support study objectives.
• Drives site activation and startup activities with regulatory, startup and in-house teams.
• Monitors quality and compliance, identifies risks, and implements mitigation plans.
• Reviews monitoring reports and ensures timely follow-up of findings.
• Develops training for study staff and supports CRA development.
• Analyzes study metrics and trends to improve execution across regions.
• Ensures regulatory compliance, TMF quality, and inspection readiness.

Skills

Clinical research

Project management

Cross-functional leadership

ICH-GCP knowledge

Vendor management

Education

Bachelor degree in life science

Job description

IQVIA sponsor-dedicated Clinical Functional Service Partnerships team is seeking a Local Clinical Study Manager to lead and oversee trials across therapeutic areas. The role is full-time and home-based, with location options Belgium/Denmark/Netherlands/Sweden.

You will drive study delivery, manage cross-functional teams, monitor progress, ensure regulatory compliance, and maintain TMF quality, while coordinating with vendors and sites to achieve timelines and quality, in line with ICH-GCP.