Senior Clinical Trial Coordinator — Global Projects Lead

Ab Inbev Group; Quilmes; On-site; ARS 600,000 - 750,000; Full time

Job summary

Thermo Fisher Scientific in Buenos Aires is seeking a Senior Clinical Trial Coordinator to provide administrative and technical support to the Project Team, coordinating activities, serving as study lead, and training new staff. You will ensure study documentation, utilize GoBalto and eTMF, manage regulatory documents, coordinate meetings, and contribute to process improvements across trials.

Join a global team focused on innovation in clinical research, with opportunities to develop expertise

Qualifications

• High / Secondary school diploma or equivalent.
• Bachelor's degree preferred.
• 4+ years of relevant clinical trial experience.
• Equivalency, combining education and experience, may be considered.

Responsibilities

• Coordinate and oversee trial activities per task matrix.
• Perform department, country and investigator file reviews and document findings.
• Ensure tasks are on time and within budget; proactively communicate risks to leads.
• Maintain study documentation and support GoBalto & eTMF systems.
• Provide system support for GoBalto & eTMF; manage study-related reports.
• Schedule and organize client/internal meetings; document meeting minutes.
• Review and track local regulatory documents and ISF materials.
• Assist with ISF/Pharmacy binder materials and translation QC as needed.
• Attend kickoff meetings and take notes when required.

Skills

Teamwork

Organizational skills

Attention to detail

English proficiency

MS Office

GoBalto

eTMF

Clinical data systems

Education

High school diploma

Bachelor's degree preferred

Equivalency accepted

Tools

GoBalto

eTMF

MS Office

Clinical trial databases

Job description

Thermo Fisher Scientific in Buenos Aires is seeking a Senior Clinical Trial Coordinator to provide administrative and technical support to the Project Team, coordinating activities, serving as study lead, and training new staff. You will ensure study documentation, utilize GoBalto and eTMF, manage regulatory documents, coordinate meetings, and contribute to process improvements across trials.

Join a global team focused on innovation in clinical research, with opportunities to develop expertise