Clinical Trial Manager (PM) - Brazil

Medpace; São Paulo; Presencial; BRL 220 000 - 360 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Competitive compensation programs

Health, wellness, retirement, and PTO

WFH flexibility after training

Company-sponsored social events

Resumo da oferta

Medpace, a leading CRO, is expanding its São Paulo office with Clinical Trial Managers and Project Managers to join the Clinical Trial Management Group in Sao Paulo, Brazil. We offer a competitive salary/bonus program, plus equity grants that have become lucrative for our associates.

You will manage day-to-day project operations, serve as primary sponsor contact, maintain protocol knowledge, supervise cross-functional teams, review study plans and deliverables, and drive risk management and

Qualificações

• Bachelor's degree in a health-related field required; advanced degree preferred.
• 5+ years as a project/clinical trial manager within a CRO.
• Experience in Phases 1-4; Phases 2-3 preferred.
• Fluency in English.

Responsabilidades

• Manage day-to-day operations of the project per contract and ICH/GCP.
• Serve as primary sponsor contact for operational 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.
• Review input for study protocol, edit checks, data analysis plan, and final report.
• Develop operational project plans and manage risk.
• Oversee study vendor management and site quality.
• Direct supervision of CRAs and monitoring deliverables.

Conhecimentos

English fluency

Leadership skills

Project management

Formação académica

Health-related degree

Advanced degree preferred

Descrição da oferta de emprego

Join Medpace in our Sao Paulo office! 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 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

• Bachelor’s degree in a health-related field required; 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
• Management of overall project timeline
• Bid defense experience, preferred
• Strong leadership skills
• Fluency in English

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.