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As Trial Manager, you will lead the end-to-end delivery of assigned clinical trials from our Clinical Development Centre (CDC) in Argentina – from planning and start-up through execution, data analysis and close‑out. You will set clear direction, safeguard quality and keep trial teams, sites and integral partners aligned on timelines and budget.
What you’ll bring
You are energised by leading teams towards ambitious goals, and you bring:
- A bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing or a related field.
- Previous experience in clinical trial project management within a pharmaceutical company or contract research organisation (CRO).
- Advanced English.
- Strong project management skills, including planning, prioritisation and managing trial resources.
- Solid knowledge of ICH‑GCP guidelines, regulatory requirements and clinical trial methodology.
- Excellent communication and relationship‑building skills, with the ability to align stakeholders without direct authority.
- A curious mindset,



open to new digital tools and better ways of working.

What you’ll do
You will be accountable for planning, executing and delivering your assigned trials in full compliance with ICH‑GCP and regulatory requirements. You will:
- Drive end‑to‑end planning and project management of your trials, keeping timelines, budget and quality on track from initiation to close‑out.
- Build and manage detailed trial project plans, including recruitment and retention strategies, and oversee clinical trial systems and the electronic Trial Master File (eTMF).
- Track performance through operational metrics such as enrolment rates, site performance and budget adherence – and act early to reduce operational risks.
- Coach and mentor the clinical trial team, delivering training on study protocols, operational procedures and ICH‑GCP compliance.
- Represent the CDC in trial meetings, lead cross‑functional stakeholder management

📌 Trial Manager (Buenos Aires)
🏢 Novo Nordisk A/S
📍 Buenos Aires