Senior Clinical Trials Coordinator: Docs & PM Support

Worldwide Clinical Trials; Buenos Aires; Presencial; ARS 52.819.000 - 83.001.000; Jornada completa

Descripción de la vacante

Worldwide Clinical Trials seeks a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects are performed timely and accurately.

The role requires excellent written and verbal English as well as fluency in the language of the country of location, strong interpersonal and organizational skills, and attention to detail with a minimum of two years’ related experience.

Formación

• Degree or equivalent qualification with at least two years’ experience.
• Excellent written and verbal English; fluency in the country language.
• Strong interpersonal, organizational and problem-solving skills.
• Attention to detail and commitment to quality work.

Responsabilidades

• Arrange and track system access for project team.
• Maintain and quality audit project documents on portals.
• Assist with preparation and shipment of clinical trial documentation.
• Maintain version control of project documentation and submit to trial master file.
• Assist tracking of site medical question and answer log.
• Generate and distribute minutes for sponsor and internal meetings.

Conocimientos

English proficiency

Interpersonal skills

Attention to detail

Organizational skills

Problem-solving skills

Educación

Bachelor's degree or equivalent

Descripción del empleo

Worldwide Clinical Trials seeks a Senior Clinical Trials Associate to provide administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects are performed timely and accurately.

The role requires excellent written and verbal English as well as fluency in the language of the country of location, strong interpersonal and organizational skills, and attention to detail with a minimum of two years’ related experience.