Clinical Trial Operations Specialist

Novo Nordisk A/S; Buenos Aires; Híbrido; ARS 1.200.000 - 1.700.000; Jornada completa

Descripción de la vacante

Novo Nordisk A/S in Buenos Aires seeks a Clinical Trial Administrator to be the operational backbone of our local study team, ensuring trials are set up, executed and closed out with precision and full regulatory compliance. You will collaborate with sites, vendors and cross-functional colleagues to keep our clinical activities running smoothly.

Day-to-day you will provide administrative and logistical support across all trial phases, maintain eTMF/ISF/Investigator Portal, assist with regulatory

Formación

• Bachelor's degree in life sciences or related field.
• Experience from pharma or CRO preferred.
• Understanding of trial phases, GCP and ethical considerations.
• Proficiency with CTMS and digital tools.
• Advanced English in writing and speaking.
• Ability to manage multiple tasks and stakeholders.

Responsabilidades

• Provide administrative, logistical and operational support across all trial phases.
• Set up and maintain eTMF, ISF and Investigator Portal; ensure archiving quality.
• Support study start-up, including regulatory submissions and 'Green Light' checks.
• Coordinate clinical supply activities and liaise on contracting and site payments.
• Prepare local Investigator Meetings and distribute study communications.
• Support inspection readiness and audits per ICH-GCP and SOPs.

Conocimientos

Attention to detail

English proficiency

Stakeholder management

Organisational skills

Educación

Bachelor's degree in life sciences

Herramientas

CTMS

Descripción del empleo

Novo Nordisk A/S in Buenos Aires seeks a Clinical Trial Administrator to be the operational backbone of our local study team, ensuring trials are set up, executed and closed out with precision and full regulatory compliance. You will collaborate with sites, vendors and cross-functional colleagues to keep our clinical activities running smoothly.

Day-to-day you will provide administrative and logistical support across all trial phases, maintain eTMF/ISF/Investigator Portal, assist with regulatory