Remote Clinical Trial Associate (CDMX)

ICON Strategic Solutions; Ciudad de México; Hybrid; MXN 420.000 - 600.000; Vollzeit

Benefits dieser Stelle

Health insurance

Annual leave entitlements

Retirement planning

Global Employee Assistance Programme (

Life assurance

Country-specific benefits

Zusammenfassung

ICON Strategic Solutions is seeking a Clinical Trial Associate to support the design and analysis of clinical trials and to interpret complex medical data from a home-based role in Mexico City. You will contribute to advancing treatments and therapies by delivering high-standard research work and collaborating with the team and stakeholders.

You will coordinate trial activities, maintain essential documents, assist with informed consent and case report forms, and help track trial metrics while

Qualifikationen

• Bachelor's degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast-paced environment with attention to detail.
• Willingness to travel as required (approximately 10%)

Aufgaben

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Kenntnisse

Organizational skills

Communication skills

Team collaboration

Attention to detail

Willingness to travel

Ausbildung

Bachelor's degree in a scientific or healthcare-related field

Jobbeschreibung

ICON Strategic Solutions is seeking a Clinical Trial Associate to support the design and analysis of clinical trials and to interpret complex medical data from a home-based role in Mexico City. You will contribute to advancing treatments and therapies by delivering high-standard research work and collaborating with the team and stakeholders.

You will coordinate trial activities, maintain essential documents, assist with informed consent and case report forms, and help track trial metrics while