Emerging Clinical Start-Up Associate Argentina

ICON Strategic Solutions; Argentina; Presencial; ARS 600.000 - 900.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Employee Assistance Programme LifeWork

Life assurance

Flexible country-specific benefits

Descripción de la vacante

ICON Strategic Solutions is seeking a Study Start Up Associate I in Argentina to support site start-up and activation for clinical trials. You will collaborate with cross-functional teams to ensure regulatory compliance and timely study initiation, contributing to innovative therapies that benefit patients worldwide.

The role emphasizes detailed regulatory documentation, stakeholder coordination, and meticulous record-keeping in a dynamic sponsor-dedicated environment.

Formación

• Bachelor's degree in life sciences or related field.
• Strong attention to detail and organizational skills.
• Excellent communication and interpersonal skills with the ability to collaborate with cross-functional teams.

Responsabilidades

• Assisting in preparation and submission of regulatory documents such as clinical trial applications and ethics committee submissions.
• Coordinating with internal and external stakeholders to obtain necessary approvals for study initiation.
• Maintaining accurate and up-to-date records of regulatory submissions and approvals.
• Supporting study teams in developing study documents including protocols, informed consent forms, and investigator brochures.
• Participating in study start-up meetings and providing input on regulatory requirements and timelines.

Conocimientos

Attention to detail

Communication

Educación

Bachelor's degree in life sciences

Descripción del empleo

ICON Strategic Solutions is seeking a Study Start Up Associate I in Argentina to support site start-up and activation for clinical trials. You will collaborate with cross-functional teams to ensure regulatory compliance and timely study initiation, contributing to innovative therapies that benefit patients worldwide.

The role emphasizes detailed regulatory documentation, stakeholder coordination, and meticulous record-keeping in a dynamic sponsor-dedicated environment.