Senior ERP Data Migration Lead (S/4HANA) - Remote

Maxit Consulting - Max Corporate Group; La Pampa; Remote; ARS 136,687,000 - 212,624,000; Full time

Benefits offered by this job

Connectivity allowance

Gym reimbursement

PedidosYa credit

Statutory vacation

Health insurance

Job summary

IQVIA is seeking a Centralized Monitoring Lead for LATAM, with remote work options. You will guide the centralized monitoring team, oversee clinical deliverables, and support study analytics. The role requires leadership across global projects and regulatory knowledge. Strong communication is essential.

You will mentor staff, coordinate resources, and drive process improvements while ensuring compliance with SOPs and regulations. This is a remote, international opportunity within a global firm.

Qualifications

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on-site).
• +2 years in a Lead role.
• Strong written and verbal communication skills including advanced command of English.
• Strong organizational, problem solving and decision making skills.
• Results and detail-oriented approach to work delivery.
• Excellent motivational, influencing, negotiating and coaching skills.

Responsibilities

• Lead the Centralized Monitoring team and oversee clinical deliverables on global projects.
• Act as Unblinded Clinical Lead; manage IPs and regulatory needs.
• Mentor junior staff and manage project resources.
• Develop monitoring strategy and analytics approach; support RBM tools.
• Attend study/client meetings and drive continuous process improvements.
• Ensure documentation and eTMF readiness; coordinate data migration activities.

Skills

Leadership

Project management

Clinical monitoring

English (Advanced)

Communication

Organizational skills

Problem solving

Coaching

Influencing

Negotiation

Education

Bachelor's degree in life sciences

Job description

IQVIA is seeking a Centralized Monitoring Lead for LATAM, with remote work options. You will guide the centralized monitoring team, oversee clinical deliverables, and support study analytics. The role requires leadership across global projects and regulatory knowledge. Strong communication is essential.

You will mentor staff, coordinate resources, and drive process improvements while ensuring compliance with SOPs and regulations. This is a remote, international opportunity within a global firm.