Remote Centralized Monitoring Lead – LATAM

Uptalent.Io; Santa Fe Capital; Remote; ARS 137,157,000 - 198,116,000; Full time

Job summary

IQVIA is seeking a Centralized Monitoring Lead for LATAM to partner with project and clinical leads to achieve study objectives while optimizing speed, quality and cost in line with IQVIA SOPs.

The role oversees a global monitoring team, mentors junior staff, and ensures compliant study documentation and RBM tools across multiple projects. Strong English, leadership, and organizational skills are essential.

Qualifications

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on site CRA). Advanced knowledge of clinical trial conduct and regulatory requirements (ICH GCP, local laws).
• +2 years in a Lead role.
• Strong written and verbal communication skills including advanced command of English (Mandatory).
• Strong organizational, problem solving and decision making skills.
• Results- and detail-oriented approach to work delivery and output.
• Excellent motivational, influencing, negotiating and coaching skills.
• Ability to work on multiple global projects and manage competing priorities.
• To lead team and effectively work in team.

Responsibilities

• Lead the Centralized Monitoring team and oversee deliverables per protocol and SOPs.
• Act as Unblinded Clinical Lead when required and manage IP for assigned studies.
• Manage project resources (CRAs, Central Monitors, CLAs).
• Monitor study/site metrics and trend analysis; develop action plans.
• Develop analytics strategy and contribute to advanced analytics.
• Support monitoring strategy development and monitoring triggers.
• Attend study team and client meetings.
• Mentor junior staff and support continuous process improvements.

Skills

Clinical monitoring

Leadership

English proficiency

Education

Bachelor's degree in life sciences or related field

Job description

IQVIA is seeking a Centralized Monitoring Lead for LATAM to partner with project and clinical leads to achieve study objectives while optimizing speed, quality and cost in line with IQVIA SOPs.

The role oversees a global monitoring team, mentors junior staff, and ensures compliant study documentation and RBM tools across multiple projects. Strong English, leadership, and organizational skills are essential.