Senior Clinical Research Associate: Site Leader & Compliance

MSD LATAM

Santiago

Híbrido

CLP 36.000.000 - 60.000.000

Jornada completa

Hace 7 días
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Descripción de la vacante

MSD LATAM in Chile is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee the performance, quality, and compliance of trial sites and protocols.

You will be the primary contact for investigators and site staff, guiding site activities through the study lifecycle. You will work with cross-functional teams to ensure data quality, patient safety, and regulatory compliance, while mentoring junior CRAs and identifying new site opportunities.

Formación

  • Bachelor’s degree or higher required.
  • At least 4 years of direct site management (monitoring) experience in pharma, biotech, or CRO.
  • Strong communication, problem-solving, and organizational skills; ability to work independently.
  • Domestic and international travel up to 65-75% may be required.

Responsabilidades

  • Site selection, start-up, monitoring, regulatory document management and issue resolution.
  • Data quality oversight and patient safety protection throughout the study lifecycle.
  • Collaborate with cross-functional teams and stakeholders to support study execution.
  • Mentor junior CRAs and identify new site opportunities; support audits and inspections.

Conocimientos

Site monitoring
Site management
Communication skills
Problem-solving
Organizational skills
Independent work
Mentoring junior CRAs
Cross-functional collaboration
Audit support
Site start-up & close-out
Regulatory document management
Patient safety awareness
Study lifecycle oversight

Educación

Bachelor’s degree or higher

Descripción del empleo

MSD LATAM in Chile is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee the performance, quality, and compliance of trial sites and protocols.

You will be the primary contact for investigators and site staff, guiding site activities through the study lifecycle. You will work with cross-functional teams to ensure data quality, patient safety, and regulatory compliance, while mentoring junior CRAs and identifying new site opportunities.

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