Clinical Research Associate – PACE Training & Travel

Medpace, Inc.; Buenos Aires; Presencial; ARS 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

Medpace is seeking a Clinical Research Associate in Buenos Aires to join our research-driven team. This role offers an exciting career in drug and medical device development, with travel across Argentina and entry into Medpace's CRA training program (PACE).

No clinical experience may be required for the training pathway, with comprehensive initial and ongoing training. The successful candidate will support site visits, data verification, and regulatory compliance across multiple therapeutic

Formación

• Bachelor's degree in a health or science related field.
• Experience in clinical monitoring preferred.
• Excellent verbal and written communication skills in Spanish and English.
• We kindly ask to send applications in English.

Responsabilidades

• Conduct qualification, initiation, monitoring, and closeout visits for research sites.
• Communication with the medical site staff including coordinators and clinical research physicians.
• Verifying adequate investigator qualifications, training and resources, including facilities and staff.
• Medical record and source documentation verification against case report forms per SOPs, GCP and regulatory requirements.
• Verification that the investigator is enrolling only eligible subjects.
• Regulatory document review and drug accountability.

Conocimientos

Clinical monitoring

Spanish-English communication

Travel willingness

Educación

Bachelor's degree in health or life sciences

Descripción del empleo

Medpace is seeking a Clinical Research Associate in Buenos Aires to join our research-driven team. This role offers an exciting career in drug and medical device development, with travel across Argentina and entry into Medpace's CRA training program (PACE).

No clinical experience may be required for the training pathway, with comprehensive initial and ongoing training. The successful candidate will support site visits, data verification, and regulatory compliance across multiple therapeutic