Department

SSU & Maintenance, Clinical Development Centre, Research & Development

Location

Bogotá, Colombia

Your impact begins here

As Clinical Research Associate Senior, you will oversee and manage clinical research sites across Colombia, ensuring the integrity of clinical data and the safety of every trial participant. Your monitoring expertise and risk-based approach will help Novo Nordisk advance trials that bring innovative treatments closer to people living with serious chronic diseases. You will be the primary link between research sites and the organisation — driving quality, building trust and keeping progress on track where it matters most.

What you'll bring
- A degree in Chemistry, Pharmacy, Biology, Pharmaceutical Engineering, Nutrition, Medicine or a related health sciences discipline.
- At least 4 years of experience in on-site monitoring activities within clinical research.
- Full understanding of ICH Good Clinical Practice (GCP) guidelines and local Colombian clinical trial regulations.
- Strong negotiation, communication and presentation skills,



with the ability to build and maintain effective relationships with internal and external stakeholders.
- Proven decision-making and problem-solving capabilities, with a quality-first mindset.
- The ability to manage multiple priorities and adapt quickly to changing conditions.
- Fluent English and Spanish — both written and spoken.

Useful, but not essential:
- Experience mentoring or training less experienced colleagues or site staff.
- Familiarity with digital monitoring tools and a strong interest in innovation within clinical operations.

What you'll do

You will manage the full monitoring lifecycle for assigned clinical research sites — from selection through to close-out — using a risk-based approach to focus effort where it has the greatest impact on data integrity and participant safety.
- Conduct site selection, initiation, routine monitoring and close-out visits in line with study protocols,

📌 CRA Sr (Bogotá)
🏢 Novo Nordisk
📍 Bogotá