Remote Oncology Clinical Research Associate

Parexel; Lansing (MI); Presencial; USD 70 000 - 110 000; Tempo integral

Resumo da oferta

Parexel is hiring a Clinical Research Associate to manage site relationships and oversee regulatory documentation across study phases. You will ensure data accuracy, subject safety, and alignment with protocol requirements while coordinating with sponsors and investigators.

The role emphasizes strong communication, travel readiness, and adherence to ICH-GCP standards. The position requires at least 2 years of direct site monitoring experience, a science-focused degree, and proficiency with

Qualificações

• Minimum 2 years of direct site monitoring experience.
• Experience with ICH-GCP and regulatory documentation.

Responsabilidades

• Act as the primary site contact and site manager throughout all phases of a clinical study.
• Perform site visits (validation, initiation, monitoring, closeout) and generate visit reports.
• Manage regulatory documentation start-up, maintenance, and close-out.

Conhecimentos

Site management

Monitoring expertise

Regulatory compliance

Communication skills

Time management

Data review

Travel readiness

Problem solving

Team mentoring

Independent work

Formação académica

Bachelor's degree preferred in science/biology

Ferramentas

MS Office

Clinical Trial Management System

Descrição da oferta de emprego

Parexel is hiring a Clinical Research Associate to manage site relationships and oversee regulatory documentation across study phases. You will ensure data accuracy, subject safety, and alignment with protocol requirements while coordinating with sponsors and investigators.

The role emphasizes strong communication, travel readiness, and adherence to ICH-GCP standards. The position requires at least 2 years of direct site monitoring experience, a science-focused degree, and proficiency with