Lead Clinical Trial Site Monitor

Parexel; Ohio; Híbrido; USD 70.000 - 95.000; Jornada completa

Descripción de la vacante

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, ensure patient safety, and drive study quality. You will monitor activities across site initiation to close-out, working with the SCP and study team to maintain protocol adherence and data integrity.

The role requires 2+ years of site monitoring experience, fluent English, and the ability to travel 60-80% of the time. Bachelor's degree in life sciences is required.

Formación

• Minimum 2 years of clinical research site monitoring experience.
• Fluent in English and local language(s) of the country of work.
• Willingness to travel 60-80% of the time.
• Bachelor's degree in life sciences or related field.

Responsabilidades

• Monitor assigned investigator sites from activation through to database lock.
• Ensure patient safety and data quality per GCP and SMP guidelines.
• Coordinate with Site Care Partner and study team for site management.
• Submit site documentation, reports and close-out activities as required.
• Address protocol questions and manage site issues with CAPA when needed.
• Oversee investigational product receipt, handling and storage at sites.

Conocimientos

Monitoring experience

English fluency

Educación

Bachelor's degree in life sciences

Descripción del empleo

Parexel is seeking a Clinical Research Associate (CRA) to manage investigator sites, ensure patient safety, and drive study quality. You will monitor activities across site initiation to close-out, working with the SCP and study team to maintain protocol adherence and data integrity.

The role requires 2+ years of site monitoring experience, fluent English, and the ability to travel 60-80% of the time. Bachelor's degree in life sciences is required.