Remote Global Clinical Trial Leader

Parexel International; Wien; Hybrid; EUR 90.000 - 120.000; Vollzeit

Zusammenfassung

Parexel International is seeking a Global Clinical Trial Leader (CTL) to join our team in a remote capacity in Austria. You will support clinical research activities, drive study execution, patient safety oversight, and regulatory compliance across international trials.

The role focuses on planning, implementation, risk mitigation, and collaboration with cross-functional teams to deliver high-quality trial data and timely results. Strong communication and a patient-focused mindset are essential.

Qualifikationen

• Master's degree preferred with minimum 5 years in clinical trial management
• Strong project management experience in international trials
• Knowledge of ICH‑GCP, regulatory requirements, and clinical trial processes
• Excellent communication, organization and problem-solving skills
• Fluency in English, both written and spoken
• Experience in Oncology, CNS, Immunology or Vaccines preferred

Aufgaben

• Plan, implement and track clinical trial processes and risk mitigation.
• Oversee trial feasibility and country allocations.
• Develop trial-level engagement plans and core documents for stakeholders.
• Ensure compliance with GCP, SOPs and regulatory requirements; monitor safety reporting.
• Coordinate amendments, training materials, and archiving of essential TMF documents.
• Support data delivery, CTR preparation, and results disclosure of global registries.

Kenntnisse

Project management

Cross-functional collaboration

Attention to detail

Communication skills

Fluency in English

Ausbildung

Master's degree (preferred)

Jobbeschreibung

Parexel International is seeking a Global Clinical Trial Leader (CTL) to join our team in a remote capacity in Austria. You will support clinical research activities, drive study execution, patient safety oversight, and regulatory compliance across international trials.

The role focuses on planning, implementation, risk mitigation, and collaboration with cross-functional teams to deliver high-quality trial data and timely results. Strong communication and a patient-focused mindset are essential.