Grants & Programs Lead

Boys & Girls Clubs Of America; San Juan; A distancia; ARS 135.820.000 - 181.094.000; Jornada completa

Descripción de la vacante

IQVIA seeks a Centralized Monitoring Lead for LATAM who will oversee the Centralized Monitoring team across multiple countries. The role involves partnering with project and clinical leads to ensure on-time, high-quality delivery in line with contract requirements and IQVIA SOPs.

The candidate should have a life sciences degree, 3+ years in clinical monitoring, 2+ years in a Lead role, and excellent English communication skills. This is a remote, international position supporting global projects.

Formación

• Bachelor’s degree in life sciences or related field is required.
• +3 years of relevant clinical monitoring experience (remote or on-site).
• +2 years in a Lead role.
• Strong written and verbal English communication.
• Ability to manage multiple global projects and teams.

Responsabilidades

• Lead the Centralized Monitoring team and coordinate with project and clinical leads per protocol and regulations.
• Monitor study/site metrics, develop analytics strategy, and implement action plans.
• Attend study team or client meetings and contribute to process improvements.
• Support RBM tools/templates development and ensure audit-ready documentation.
• Mentor junior staff and coach team members.

Conocimientos

Leadership

English mandatory

Project management

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.

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