Strategic Project Manager — Clinical Trials & SDLC

Signant Health, Inc.; Santiago; Presencial; CLP 53.715.309 - 71.620.412; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Collaborative global environment

Opportunities for career growth

Purpose-driven work

Descripción de la vacante

Signant Health, Inc. is seeking a Project Manager responsible for planning, execution, and delivery of various projects across its solutions. The role involves managing the full software development lifecycle (SDLC) while ensuring adherence to project budgets and timelines.

The ideal candidate will excel at problem-solving, lead cross-functional teams, and manage client communications effectively. Experience in a regulated industry is mandatory, and proficiency with project management tools is essential. This is an exciting opportunity to have a significant impact in the clinical trial space.

Formación

• Proven experience managing end-to-end projects in a regulated industry.
• Strong understanding of the software development lifecycle (SDLC).
• Hands-on experience with project management tools.

Responsabilidades

• Manage and lead project delivery across multiple product lines.
• Oversee the full SDLC, ensuring client specifications are met.
• Lead client communications and handle escalations.

Conocimientos

Budget management and forecasting

Risk identification and assessment

Excellent verbal and written communication

Analytical and problem-solving skills

Project management tools (Jira, MS Project)

Educación

Bachelor’s degree in Computer Science, Life Sciences, Project Management, or related field

Herramientas

Jira

MS Project

Asana

Monday

Trello

Descripción del empleo

Signant Health, Inc. is seeking a Project Manager responsible for planning, execution, and delivery of various projects across its solutions. The role involves managing the full software development lifecycle (SDLC) while ensuring adherence to project budgets and timelines.

The ideal candidate will excel at problem-solving, lead cross-functional teams, and manage client communications effectively. Experience in a regulated industry is mandatory, and proficiency with project management tools is essential. This is an exciting opportunity to have a significant impact in the clinical trial space.