Home-based Local Clinical Study Manager – Oncology (EU)

IQVIA; Basel; Ibrido; CHF 120.000 - 180.000; Tempo pieno

Descrizione del lavoro

IQVIA is seeking a Local Clinical Study Manager for a sponsor-dedicated Clinical FSP. The role is full-time and home-based, with possible locations in Belgium, Denmark, Netherlands, or Sweden.

You will oversee operational and scientific aspects, including trial setup, execution, and delivery at the local level, collaborating with regulatory, QA, and clinical teams. Responsibilities include leading cross-functional teams, monitoring progress, managing sites and vendors, and ensuring ICH-GCP

Competenze

• Bachelor degree in life sciences or related discipline.
• 5+ years in clinical research with at least 2 years in project management.
• Solid knowledge of ICH GCP and local regulations.
• Proven ability to lead cross-functional teams to deliver trials on time and on budget.
• Experience in Oncology or Onco-hematology is required.
• Excellent spoken and written English and local language.

Mansioni

• Provide overall leadership and oversight for trial delivery, quality, timelines and outcomes.
• Lead cross-functional teams, set priorities, and ensure effective communication.
• Plan and oversee monitoring activities, provide status updates and drive progress.
• Manage vendors and budgets, coordinate resources to support study objectives.
• Drive site activation and startup activities with regulatory and in-house teams.
• Ensure regulatory compliance and trial master file quality, risk mitigation and issue resolution.

Conoscenze

Cross-functional leadership

Project management

English language proficiency

Stakeholder management

Formazione

Bachelor's in life sciences

Strumenti

CTMS

Descrizione del lavoro

IQVIA is seeking a Local Clinical Study Manager for a sponsor-dedicated Clinical FSP. The role is full-time and home-based, with possible locations in Belgium, Denmark, Netherlands, or Sweden.

You will oversee operational and scientific aspects, including trial setup, execution, and delivery at the local level, collaborating with regulatory, QA, and clinical teams. Responsibilities include leading cross-functional teams, monitoring progress, managing sites and vendors, and ensuring ICH-GCP