Senior Clinical Research Associate — Lead Site Monitors

Ctifacts; Buenos Aires; Hybrid; ARS 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Tuition assistance

Hybrid work from home schedule

Paid parental leave

Mentoring program and career growth

Job summary

Ctifacts in Buenos Aires, Argentina is seeking a Senior Clinical Research Associate. The role focuses on site monitoring, regulatory compliance, and study start-up activities across assigned sites, with travel to study sites as needed.

The ideal candidate has 3 years of CRA experience and a relevant degree; responsibilities include managing site visits, data integrity, and collaboration with cross-functional teams. This is a dynamic, culture-driven environment with opportunities for growth.

Qualifications

• 3 years of clinical trial monitoring experience or equivalent, as determined by CTI Management and HR.
• Bachelor's Degree or higher in allied health field, or RN with Associates or Nursing Diploma with experience.
• Previous experience in conducting clinical research studies in hospital, pharma, or CRO.

Responsibilities

• Serve as main CTI contact for assigned study sites.
• Conduct PSV, SIV, IMV, and COV visits with timely deliverables per Monitoring Plan.
• Assist with feasibility, site selection, and start-up activities.
• Collect, review and track essential documents; manage IP and trial materials.
• Participate in trainings, meetings and sponsor/client updates; may present.
• Develop subject enrollment strategies; monitor site status and SDV processes.
• Perform translation/review of patient information and consent forms as required.
• Support regulatory submissions and ethics committee processes as needed.

Skills

Clinical trial monitoring

Education

Bachelor's degree or higher in allied health

Job description

Ctifacts in Buenos Aires, Argentina is seeking a Senior Clinical Research Associate. The role focuses on site monitoring, regulatory compliance, and study start-up activities across assigned sites, with travel to study sites as needed.

The ideal candidate has 3 years of CRA experience and a relevant degree; responsibilities include managing site visits, data integrity, and collaboration with cross-functional teams. This is a dynamic, culture-driven environment with opportunities for growth.