Profesor De Estadística: Clases Remotas, Horarios Flexibles

Sercanto srl; Partido de Quilmes; Híbrido; ARS 137.157.000 - 198.116.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Centralized Monitoring Lead for LATAM on a remote basis. You will lead the Centralized Monitoring team, partner with project and clinical leads, and ensure delivery excellence across global projects in line with IQVIA SOPs and regulatory requirements.

The role requires at least 3 years in clinical monitoring with a lead-level track record, strong English communication, and a proven ability to manage cross-functional resources across multiple regions.

Formación

• Strong written and verbal communication; advanced command of English.
• Proven leadership and team coordination abilities.
• Experience leading clinical monitoring activities and RBM initiatives.

Responsabilidades

• Lead the Centralized Monitoring team and oversee global clinical deliverables.
• Act as Clinical Lead when needed and manage IP-related tasks.
• Manage project resources (CRAs, Central Monitors, CTA/CMAs).
• Develop study analytics strategy and monitor metrics/trends.
• Support monitoring strategy development and attend client/study meetings.
• Provide guidance to study teams and drive continuous process improvements.
• Develop and use study management RBM tools and templates.
• Mentor junior staff and ensure audit readiness.

Conocimientos

English proficiency

Leadership

Team leadership

Mentoring

Multitasking

Organizational skills

Attention to detail

Communication

Problem solving

Educación

Bachelor's degree in life sciences

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 there is 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.

#LI-NRJ #LI-Remote

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

Location & Work Schedule

Location: Remote - LATAM (Argentina, Brazil, Perú, Colombia)

Work Schedule: Monday-Friday, 8:00 AM-5:00 PM CST/EST

Compensation & Benefits

Final compensation will be based on experience and geographic location.

Kelly is an equal opportunity employer committed to building a diverse, equitable, and inclusive workforce, including individuals of all races, genders, abilities, protected veteran status, sexual orientations, and gender identities. Equal Employment Opportunity is the Law.