Remote & On-Site Clinical Research Associate

Thermo Fisher Scientific Inc.; Madrid; Presencial; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific Inc. is seeking a Clinical Research Associate to coordinate clinical monitoring and site management. You will conduct on-site or remote visits to ensure protocol and regulatory compliance and maintain required documentation.

As a CRA I, you’ll collaborate with sponsors, support audit readiness, and work with cross-functional teams to ensure subject safety and data integrity in a dynamic, global environment.

Formación

• Bachelor's degree in life sciences or RN certification or equivalent.
• Minimal clinical monitoring experience (≈2 years) in a clinical setting with trials/medical terminology.
• Valid driver's license where applicable.
• Equivalency may be considered for the role.

Responsabilidades

• Monitor investigator sites using a risk-based monitoring approach and conduct SDR/SDV/CRF reviews.
• Participate in investigator meetings and help identify qualified sites; initiate and close out trial sites.
• Ensure essential documents are complete per ICH-GCP and applicable regulations; conduct on-site file reviews.
• Provide trial status updates and ensure study systems are complete and updated per conventions.
• Facilitate communication between investigative sites, client, and internal teams; respond to audits/inspections.
• Maintain administrative tasks such as expense reports and timesheets.
• Contribute to project publications/tools and participate in process improvement initiatives.

Conocimientos

Medical terminology

ICH-GCP knowledge

Communication skills

Interpersonal skills

Time management

Attention to detail

Critical thinking

Risk-based monitoring

Team collaboration

Computer skills

Educación

Bachelor's degree in life sciences

Registered Nursing certification

Equivalent education/experience

Herramientas

Microsoft Office

Descripción del empleo

Thermo Fisher Scientific Inc. is seeking a Clinical Research Associate to coordinate clinical monitoring and site management. You will conduct on-site or remote visits to ensure protocol and regulatory compliance and maintain required documentation.

As a CRA I, you’ll collaborate with sponsors, support audit readiness, and work with cross-functional teams to ensure subject safety and data integrity in a dynamic, global environment.