Trial Manager

Clinical Trials Department

Vicente Lopez, Buenos Aires

Step into a role where every plan you build, every milestone you reach, and every decision you make moves a clinical trial closer to the patients waiting for new treatment options. As a Trial Manager, you will be the driving force behind end-to-end trial delivery – setting direction, safeguarding quality, and bringing teams together around a shared purpose. Are you ready to lead clinical trials that shape the future of healthcare?

Your new role
As a CDC Trial Manager, you will be accountable for the planning, execution, and successful delivery of assigned clinical trials within the CDC. You will champion operational excellence, uphold quality, and build strong partnerships across internal teams and external stakeholders – all while ensuring full compliance with ICH-GCP and regulatory requirements.

Your day-to-day responsibilities will include:

• Driving end-to-end planning and project management of assigned clinical trials, from initiation through execution, data analysis and close-out – ensuring alignment with timelines, budget and quality standards
• Developing and managing detailed trial project plans, including recruitment and retention strategies and oversight of clinical trial systems and the eTMF
• Monitoring trial performance through operational metrics such as enrolment rates, site performance and budget adherence, and proactively mitigating operational risks
• Coaching and mentoring the clinical trial team, delivering training on study protocols, operational procedures and ICH-GCP compliance
• Representing the CDC in trial meetings, leading cross-functional stakeholder management and organising CDC Investigator Meetings
• Liaising with study start-up to define submission strategy to Regulatory Authorities and Ethics Committees, while providing operational insight and local intelligence to global stakeholders
• Embedding a risk-based approach to quality management, ensuring inspection readiness and supporting audits and inspections throughout the trial lifecycle

Your new department

You will join our Clinical Operations department, working closely with trial squads, the Global Project Team, regional and HQ clinical teams, and key cross-functional partners. Reporting to the TA Lead, you will play a central role in ensuring our clinical trials are delivered with precision, integrity and impact – directly contributing to the therapies that reach millions of patients living with serious chronic diseases.

Your skills & qualifications
We are looking for a Trial Manager who is energised by leading teams toward ambitious goals. You bring with you:

• Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing or a related fields.
• Previous experience in clinical trial project management within a pharmaceutical company or CRO, ideally across more than one phase of development.
• Strong clinical trial project management skills, including organisation, planning and prioritisation, with a proven ability to manage trial resources efficiently.
• Solid knowledge of ICH-GCP guidelines, regulatory requirements and clinical trial methodology.
• Advanced level of English.
• Excellent communication and relationship-building skills, with the ability to lead without direct authority and align stakeholders across organisational levels.
• A curious, enterprise mindset – open to new digital tools, creative problem-solving and continuous improvement of processes and outcomes.

Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

What we offer
There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

Deadline
9 June 2026. CVs are reviewed on an ongoing basis.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.