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Medpace

Global CRO delivering full-service clinical trials

Clinical Trial Manager - Oncology

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeSingaporeNo salary listed

About the Job

Requirements

  • A bachelor's degree in a health or life science-related field is required.
  • At least two years of clinical trial management experience in the Asia Pacific region, ideally in a contract research organization environment, is required.
  • Experience in oncology studies is required.
  • Excellent written and spoken English is required.
  • The candidate must be flexible, accountable, and comfortable working in a global environment.

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.
  • Maintain in-depth knowledge of the protocol, therapeutic area, and indication.
  • Provide cross-functional oversight of internal project team members and deliverables, including ensuring that 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 directly supervising project Clinical Research Associates and monitoring deliverables.

Desired Qualifications

  • An advanced degree in a health or life science-related field is preferred.
  • Clinical trial management experience in a contract research organization environment is ideally desired.

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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