Clinical Trial Site Coordinator - Flex Office (Mexico)

ICON Clinical Research; Ciudad de México; Presencial; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A leading clinical research organization in Ciudad de México seeks a Clinical Site Associate to support the management of clinical trials. Responsibilities include planning trial activities, coordinating with sites, and monitoring study progress. Candidates should have a Bachelor's degree in a relevant field and strong communication skills. This role offers competitive salary and benefits catered to employee well-being and work-life balance.

Servicios

Various annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Life assurance

Flexible country-specific optional benefits

Formación

• Bachelor's degree in a relevant field, such as life sciences or healthcare.
• Previous experience in clinical research.
• Strong organizational and communication skills.
• Ability to work independently and collaboratively in a fast-paced environment.
• Attention to detail and ability to prioritize tasks effectively.
• Advanced English communication - Speaking will be tested.

Responsabilidades

• Assisting in the planning, initiation, and execution of clinical trial activities.
• Conducting site feasibility assessments and participating in site selection processes.
• Coordinating with investigative sites for compliance with protocols.
• Monitoring study progress and data collection for quality and accuracy.
• Assisting in preparation and review of study documentation and reports.

Conocimientos

Strong organizational skills

Communication skills

Attention to detail

Ability to work independently

Ability to work collaboratively

Advanced English communication

Educación

Bachelor's degree in a relevant field

Descripción del empleo

A leading clinical research organization in Ciudad de México seeks a Clinical Site Associate to support the management of clinical trials. Responsibilities include planning trial activities, coordinating with sites, and monitoring study progress. Candidates should have a Bachelor's degree in a relevant field and strong communication skills. This role offers competitive salary and benefits catered to employee well-being and work-life balance.