Clinical Trial Project Manager - Brazil

Medpace; São Paulo; Híbrido; USD 60.000 - 100.000; Tempo integral

Resumo da oferta

An established industry player is seeking experienced Clinical Trial Managers to join their dynamic team in São Paulo. This role offers the chance to lead critical projects in various therapeutic areas, ensuring compliance with regulations and managing project timelines. The company values flexibility and provides a competitive salary and benefits package, including equity grants. Join a forward-thinking organization that has a significant impact on global health and contribute to the development of innovative medical solutions. If you're passionate about making a difference, this opportunity is perfect for you.

Serviços

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Qualificações

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

Responsabilidades

• Manage day-to-day operations of the project according to ICH/GCP.
• Serve as primary Sponsor contact for operational project-specific issues.

Conhecimentos

Leadership Skills

Project Management

Clinical Trial Management

Risk Assessment

Fluency in English

Formação académica

Bachelor’s degree in a health-related field

Advanced degree in a health-related field

Descrição da oferta de emprego

Job Summary

Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil. Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We provide remote flexibility with relevant experience. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

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.
• Responsible for management of study vendor.
• Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.

Qualifications

***We kindly ask that you send your CV in English***

• 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 for home-based.
• Management of overall project timeline.
• Strong leadership skills.
• Fluency in English.

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.

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