Lead Clinical Trial Manager

Novo Nordisk A/S; Partido de Vicente López; Presencial; ARS 1.800.000 - 3.000.000; Jornada completa

Descripción de la vacante

Novo Nordisk A/S is seeking an Trial Manager to lead end‑to‑end delivery of clinical trials from our CDC in Argentina. You will plan, start‑up, execute and close trials while ensuring quality, timelines and budget adherence.

You will work with cross‑functional teams, sites, and global partners, applying ICH‑GCP principles and regulatory requirements. English proficiency and strong PM skills are essential for success in this role.

Formación

• Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Nursing or related field.
• Experience in clinical trial project management within pharma or CRO.
• Advanced English.
• Strong planning, prioritisation and resource management skills.
• Solid knowledge of ICH‑GCP guidelines and regulatory requirements.
• Excellent communication and relationship-building to align stakeholders without direct authority.
• Curious mindset open to new digital tools and better ways of working.

Responsabilidades

• Drive end‑to‑end planning and project management of trials from initiation to close‑out.
• Build and manage detailed trial plans including recruitment and retention strategies.
• Oversee eTMF and clinical trial systems; monitor enrolment, site performance and budget adherence.
• Coach and mentor the trial team on study protocols and ICH‑GCP compliance.
• Represent the CDC in meetings and manage cross‑functional stakeholders.
• Support study start‑up and submissions to Regulatory Authorities and Ethics Committees.

Conocimientos

Advanced English

Project management

ICH‑GCP knowledge

Communication skills

Stakeholder alignment

Educación

Bachelor’s degree in Life Sciences or related field

Descripción del empleo

Novo Nordisk A/S is seeking an Trial Manager to lead end‑to‑end delivery of clinical trials from our CDC in Argentina. You will plan, start‑up, execute and close trials while ensuring quality, timelines and budget adherence.

You will work with cross‑functional teams, sites, and global partners, applying ICH‑GCP principles and regulatory requirements. English proficiency and strong PM skills are essential for success in this role.