Profesor Particulares Remotas: Horarios Flexibles

Sercanto srl; Partido de Quilmes; Híbrido; ARS 137.587.000 - 214.025.000; Jornada completa

Descripción de la vacante

Sercanto srl is seeking a Centralized Monitoring Lead for LATAM (Remote). You will lead the Centralized Monitoring team, partnering with the project and clinical leads to ensure delivery per contract while optimizing speed, quality and cost, in accordance with IQVIA SOPs.

Responsibilities include overseeing global projects, managing study metrics and trend analyses, mentoring junior staff, contributing to monitoring strategy and RBM tools, and ensuring audit readiness and timely study

Formación

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on-site CRA).
• +2 years in a Lead role.
• Advanced knowledge of ICH GCP and applicable local regulations.
• Strong English language skills (mandatory).

Responsabilidades

• Lead the Centralized Monitoring team and oversee deliverables on global projects.
• Manage study metrics, trend analyses and action plans.
• Mentor junior staff and coach team members.
• Support monitoring strategy development and RBM tool usage.
• Ensure audit readiness and maintain clear study documentation.
• Participate in client meetings and key decision processes.

Conocimientos

Communication skills

Leadership

Organizational skills

Problem solving

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

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.

EEO Minorities/Females/Protected Veterans/Disabled

Compensation & Benefits

• Final compensation will be based on experience and geographic location.