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Medpace

Global CRO delivering full-service clinical trials

Clinical Trial Project Manager

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeBuenos Aires, Argentina

About the Job

Requirements

  • A bachelor's degree in a health-related field is required.
  • Experience managing projects or clinical trials within a contract research organization for 2–3 years is required.
  • Experience in clinical trial Phases 1–4 is required.
  • Experience managing the overall project timeline is required.
  • Fluency in English is required.
  • Applications should be submitted in English.

Responsibilities

  • Manage and be accountable for day-to-day project operations as defined by the contract and in accordance with ICH/GCP and applicable laws, rules, and regulations.
  • Serve as the primary Sponsor contact for operational project-specific issues and study deliverables.
  • Focus on clinical deliverables rather than project financials.
  • Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
  • Provide cross-functional oversight of internal project team members and deliverables, including ensuring necessary project-specific training is provided.
  • Review and provide input for the 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.
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables.

Desired Qualifications

  • An advanced degree in a health-related field is preferred.
  • Experience in Phases 2–3 is preferred.
  • Bid defense experience is preferred.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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