Senior Global Oncology Trials Leader

Alentis Therapeutics; Allschwil; Presencial; CHF 180.000 - 260.000; Jornada completa

Descripción de la vacante

Alentis Therapeutics is seeking a Senior Clinical Trial Leader Oncology to lead complex global trials, manage CROs, and ensure regulatory compliance. You will oversee study planning, documentation, safety monitoring, and cross-functional coordination across development programs.

A Master’s degree and 8+ years of experience in biotech-related clinical development are required, with English fluency and international travel ability.

Formación

• Master's degree or equivalent in Life Sciences, Healthcare, Pharmacy, or related field.
• ≥8 years of clinical study management experience, including early-phase trials, preferably in biotech/global development.
• Leadership and stakeholder management across countries, functions and vendors.
• Strong knowledge of oncology drug development and ICH-GCP.
• Experience managing CROs and external service providers.

Responsabilidades

• Act as the primary Clinical Operations/Clinical Science lead for external vendors and study partners.
• Lead global clinical trials, ensuring timelines, budget, quality and regulatory compliance.
• Provide strategic leadership for one or more studies and align development programs.
• Oversee study documents, regulatory submissions, and monitoring plans.
• Coordinate safety data monitoring and risk management with clinical teams.
• Manage forecasting of IMP, supplies, and study materials.

Conocimientos

Clinical trial leadership

Project management

Vendor management

Global development

Regulatory knowledge

Educación

Master's degree in Life Sciences or related field

Descripción del empleo

Alentis Therapeutics is seeking a Senior Clinical Trial Leader Oncology to lead complex global trials, manage CROs, and ensure regulatory compliance. You will oversee study planning, documentation, safety monitoring, and cross-functional coordination across development programs.

A Master’s degree and 8+ years of experience in biotech-related clinical development are required, with English fluency and international travel ability.