Associate Clinical Project Manager (Oncology/Respiratory)

Location: Zaventem, Belgium; candidates must be based in the listed location. The role requires national and international travel.

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Lead Local Study Teams consisting of CRAs and CSAs at country level.
• Manage country study commitments, timelines, budgets, quality, and compliance with sponsor procedures, ICH-GCP, and local regulations.
• Coordinate site identification, feasibility, qualification, activation, monitoring, close-out, and essential document archiving.
• Manage regulatory and ethics submissions, informed consent documentation, contracts, budgets, and local drug activities.
• Oversee monitoring activities, review monitoring reports, and support co-monitoring and training visits when required.
• Identify study risks, resolve complex issues, and organize regular Local Study Team meetings.

Requirements

• Bachelor’s degree in a related discipline, preferably life sciences, or an equivalent qualification.
• At least one year of local-level Clinical Project Management experience.
• Very good knowledge of oncology or respiratory therapeutic areas and experience with Phase III clinical trials.
• Strong understanding of the clinical study process, including monitoring, project management, prioritization, negotiation, and cross-functional leadership.
• Very good spoken and written English plus French or Dutch is required.
• Ability to learn and use IT systems and travel nationally and internationally as required.

Culture & Benefits

• Work in a global clinical research and healthcare intelligence organization.
• Support the development and commercialization of innovative medical treatments.
• Work within a structured sponsor-dedicated clinical study environment.
• Full-time employment with country-level responsibility and international collaboration.