Senior Clinical Studies Coordinator — PMP Required
Must-have:Senior
Machine translation — original language: Spanish.Show original
Are you a PMP certified Project Manager passionate about leading complex projects with multiple stakeholders? Join an international clinical research organization and lead the startup of clinical studies from award to implementation.
What you will do:
- Manage study startup projects and research site activation: timelines, milestones, risks, and disciplined follow-up.
- Coordinate with Regulatory, Finance, Clinical Operations, Quality, sponsors, and CROs teams.
- Maintain total project visibility through trackers, status reports, and timely escalation of risks.
- Propose continuous improvements to department processes, templates, and tools.
What we are looking for:
- Active PMP certification (indispensable) and 2–3 years of experience in project management.
- Advanced English spoken and written (indispensable).
- Degree in life sciences, health, business, or related fields (or equivalent experience).
- Experience in clinical research, health, foreign trade, or other regulated industries.
- Ability to handle multiple projects with demanding deadlines and generate accountability among areas that do not report to you.
- Proficiency in Microsoft Office and project management or document management systems.
What we offer
- Competitive salary, private medical insurance
- High-impact role with growth toward supervisory positions.
- Continuous training.
Requirements
- Minimum Education: University 3 years of experience
- Languages: English
- Age: between 30 and 45 years
- Knowledge: Coordinacion de proyectos, Inglés, Pmp, Análisis de proyectos, Gestión de proyectos clínicos
- People with disabilities: Yes
- Keywords: residente, encargado, supervisor, subgerente, responsable, coordinador, gestor, capitan, senior, sr