Global Lifecycle Safety Project Lead

IQVIA Inc; Bogotá; Presencial; COP 284 765 000 - 379 687 000; Tempo integral

Resumo da oferta

IQVIA Inc. is seeking an experienced Lifecycle Safety Program Manager to oversee delivery excellence across regional and global projects in clinical trial and post-marketing settings.

You will lead customer-facing activities, manage startups, oversee timelines, budgets, and governance, and collaborate across sales, proposal teams, and operational partners to ensure global consistency. The role requires strong leadership, PM skills, and deep knowledge of GCP/ICH and IQVIA SOPs, with 4–6 years in

Qualificações

• 4-6 years of clinical research experience in a CRO or pharmaceutical company.
• 2 years of project management experience.
• PMP certification or equivalent preferred.
• Strong knowledge of global, regional, and local clinical research regulations (GCP, ICH).
• Ability to build networks and lead teleconferences.

Responsabilidades

• Manage start-up of new projects using SOPs and best practices.
• Represent Lifecycle Safety on projects and serve as primary contact for customers.
• Oversee project planning, timelines, scope, quality, and finances.
• Act as Solution Architect for new standalone Safety opportunities.
• Develop and defend proposed solutions, pricing strategies, and budget assumptions.
• Lead meetings with stakeholders and coordinate virtual project teams.

Conhecimentos

Leadership

Project management

Communication

Stakeholder management

Negotiation

Formação académica

Bachelor’s degree in Health Sciences or related field

Ferramentas

GCP

ICH guidelines

IQVIA SOPs

Descrição da oferta de emprego

IQVIA Inc. is seeking an experienced Lifecycle Safety Program Manager to oversee delivery excellence across regional and global projects in clinical trial and post-marketing settings.

You will lead customer-facing activities, manage startups, oversee timelines, budgets, and governance, and collaborate across sales, proposal teams, and operational partners to ensure global consistency. The role requires strong leadership, PM skills, and deep knowledge of GCP/ICH and IQVIA SOPs, with 4–6 years in