¡Activa las notificaciones laborales por email!

Senior Clinical Trial Project Manager – Remote - Chile

Medpace

Chile

A distancia

USD 70.000 - 100.000

Jornada completa

Hace 7 días
Sé de los primeros/as/es en solicitar esta vacante

Mejora tus posibilidades de llegar a la entrevista

Elabora un currículum adaptado a la vacante para tener más posibilidades de triunfar.

Descripción de la vacante

Medpace is expanding its operations in South America and is looking for a Clinical Trial Manager in Chile. The ideal candidate will possess strong leadership skills and extensive experience managing clinical trials, ensuring that all aspects of the project are delivered on time and in compliance with regulations. The position offers a competitive salary and benefits package, making it an excellent opportunity for professionals in the clinical research field.

Servicios

Flexible work environment
Competitive compensation and benefits package
Competitive PTO packages
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives

Formación

  • 5+ years as a project/clinical trial manager within a CRO required.
  • Experience in Phases 1-4; Phases 2-3 preferred.
  • Management of overall project timeline.

Responsabilidades

  • Manage day-to-day operations of clinical trials.
  • Serve as the primary Sponsor contact for projects.
  • Provide oversight of internal project team members.

Conocimientos

Leadership
Project Management
Risk Assessment

Educación

Bachelor’s degree in a health-related field
Advanced degree in a health-related field

Descripción del empleo

Job Summary

Our activities in South America are expanding! Medpace is the leading CRO for Biotech companies and we are seeking to add an established Clinical Trial Manager to join our Clinical Trial Management Group in Chile. Our therapeutic areas of focus include Oncology/Hematology, Cardiovascular/Metabolic, Infectious Disease, Neuroscience, and more. We offer a very competitive salary/bonus programs along with local benefits.

Responsibilities
  • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables
  • Maintain in depth knowledge of protocol, therapeutic area, and indication
  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
  • Develop operational project plans
  • Manage risk assessment and execution
  • Manage study vendors where applicable
  • Manage site quality and monitoring deliverables
Qualifications
  • Bachelor’s degree in a health-related field; Advanced degree in a health-related field preferred
  • Experience in Phases 1-4; Phases 2-3 preferred
  • 5+ years as a project/clinical trial manager within a CRO required;
  • Management of overall project timeline;
  • Bid defense experience preferred and
  • Strong leadership skills
Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Awards

  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

Consigue la evaluación confidencial y gratuita de tu currículum.
o arrastra un archivo en formato PDF, DOC, DOCX, ODT o PAGES de hasta 5 MB.