Google Solar Integration Specialist - Remote - Latin America

Fullstack; Buenos Aires; A distancia; ARS 137.157.000 - 228.596.000; Jornada completa

Descripción de la vacante

Kelly is seeking a Centralized Monitoring Lead for LATAM with a remote work option across several countries. You will oversee the Centralized Monitoring team, collaborating with the project and clinical leads to meet contract objectives while optimizing speed, quality and cost in line with IQVIA SOPs.

The role requires leadership of study metrics, development of analytics strategies, and mentoring junior staff across regions.

Formación

• Bachelor’s degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience.
• +2 years in a Lead role.
• Strong knowledge of ICH GCP and local regulations.
• Fluent in English and strong communication.
• Ability to manage multiple global projects.

Responsabilidades

• Lead the Centralized Monitoring team and oversee deliverables.
• Mentor junior staff and manage project resources.
• Monitor study metrics and develop analytic strategies.
• Support monitoring strategy and oversee RBM tools.
• Communicate with study teams and clients; ensure compliance.
• Ensure documentation and audit readiness.

Conocimientos

Leadership

Analytics

English (Mandatory)

Team mentoring

Educación

Bachelor's degree in life sciences or related field

Descripción del empleo

Centralized Monitoring Lead in LATAM (Remote)

Buenos Aires, Argentina
Mexico City, Mexico
Santiago, Chile
Lima, Peru
São Paulo, Brazil
Bogota, Colombia
Full time
R

Job Overview

The Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project's overall objectives to the sponsor's satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance with IQVIA SOPs, policies and practices.

Essential Functions

• Leadership activities:
• Leader of the Centralized Monitoring team, partner with the project and clinical lead to perform oversight on clinical deliverables on global assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.
• Unblinded Clinical Lead, including IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.)
• May act as Clinical Lead when not assigned to the study and at project close out.
• Manage project resources (CRAs/ Central Monitors/ Clinical Trial Assistants/ Centralized Monitoring Assistants)
• Analytical activities:
• Manage, monitor and complete study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan compliance etc.).
• Contribute to developing the study specific analytics strategy and work on developing advanced analytics.
• Support project management team to develop monitoring strategy, including monitoring triggers/thresholds.
• Attend study team and /or client meetings.
• Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.
• Development and use of study management plans, and/or RBM specific tools and templates, and/or other study specific plans to evaluate the quality and integrity of the study.
• Ensure complete and accurate documentation of all the study specific tools and templates and keep the project Audit ready, including eTMF oversight.
• Mentors or coaches for junior staff.

Qualifications

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (as remote or on site CRA). Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
• +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.

EEO Minorities/Females/Protected Veterans/Disabled

Company Culture

Together, we change lives.
Kelly is a team of experts driven by our belief that the impact of the right person in the right job is limitless.
No matter where you are in your career journey, you can apply your knowledge and passion to move people, organizations, and communities forward.
You’ll have opportunities to grow your expertise and capabilities, both professionally and personally.
As a team, we celebrate inclusion, caring, and collaboration.
As a company, we value your contributions, work with integrity, and always put people first—so your impact truly will change lives.