Clinical Trial Project Manager

Medpace; Ciudad Autónoma de Buenos Aires; Presencial; ARS 9.750.000 - 12.500.000; Jornada completa

Descripción de la vacante

A leading clinical research organization in Buenos Aires is looking for a Clinical Trial Manager to oversee project operations and ensure compliance. The successful candidate will have a Bachelor's degree in a health-related field and 2-3 years of project management experience in a clinical trial setting. This role offers competitive compensation and a supporting work environment focused on professional growth.

Servicios

Flexible work environment

Competitive compensation and benefits package

Structured career paths with opportunities for professional growth

Formación

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

Responsabilidades

• Manage day-to-day operations of the project according to ICH/GCP.
• Serve as primary Sponsor contact for project-specific issues.
• Maintain knowledge of protocol, therapeutic area, and indication.

Conocimientos

Project management

Leadership

Clinical trials experience

Fluency in English

Educación

Bachelor's degree in a health-related field

Advanced degree in a health-related field

Descripción del empleo

Overview

Medpace is the leading CRO for Biotech companies and is continuing to add and established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Buenos Aires, Argentina. 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
• Focus on clinical deliverables rather than project financials
• 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 to send applications 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
• 2-3 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). 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.