Senior CRA I - Remote, 6-Month Contract

Actalent; Santa Clara (CA); A distancia; USD 81.000 - 86.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Benefits included (W2)

Descripción de la vacante

Actalent is seeking a Senior Clinical Research Associate I (Sr CRA I) for a 6-month contract (renewable or conversion to PERM). The Sr CRA I coordinates all aspects of clinical monitoring and site management, conducting remote and on-site visits to ensure protocol compliance, data integrity, and audit readiness across diverse trials.

The role emphasizes ICH-GCP compliance, collaboration with investigational sites, and effective communication with project teams.

Formación

• Bachelor's degree in life sciences or RN certification required.
• Minimum 2 years of clinical research monitoring experience.
• Willingness to travel with a valid driver's license.
• Strong knowledge of ICH-GCP and regulatory guidelines.
• Excellent written and verbal communication in English.

Responsabilidades

• Perform remote and on-site monitoring and site management.
• Apply risk-based monitoring to identify issues and implement CAPAs.
• Ensure data accuracy via SDR/SDV/CRF review.
• Manage investigator payments and documentation.
• Collaborate with project teams and investigators to ensure protocol adherence.
• Prepare trial communications and internal updates.

Conocimientos

Life sciences background

2+ years CRA experience

Driver's license

On-site & remote monitoring

ICH-GCP knowledge

Risk-based monitoring

Communication skills

Attention to detail

Time management

CTMS / Microsoft Office

English proficiency

Presentation skills

Educación

Bachelor's degree in life sciences or nursing

Herramientas

CTMS

Microsoft Office

Descripción del empleo

Actalent is seeking a Senior Clinical Research Associate I (Sr CRA I) for a 6-month contract (renewable or conversion to PERM). The Sr CRA I coordinates all aspects of clinical monitoring and site management, conducting remote and on-site visits to ensure protocol compliance, data integrity, and audit readiness across diverse trials.

The role emphasizes ICH-GCP compliance, collaboration with investigational sites, and effective communication with project teams.