Oncology Clinical Trial Manager – Singapore (Hybrid)

Medpace, Inc.

Singapore

On-site

SGD 120,000 - 180,000

Full time

14 days+

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Benefits offered by this job

Competitive compensation
Health, wellness, retirement, PTO
WFH flexibility after training
Company-sponsored social events

Job summary

Medpace is seeking a Clinical Trial Manager to oversee day-to-day project operations within our Singapore group. You will serve as the Sponsor contact for operational issues and ensure study deliverables meet ICH/GCP guidelines while coordinating cross-functional teams.

The role requires oncology trial experience, strong English communication, and a flexible, globally oriented mindset. This is an on-site position based in Singapore within a leading CRO environment.

Qualifications

  • Bachelor's degree in a health or life science-related field; advanced degree preferred.
  • At least two years of clinical trial management experience in Asia Pacific, ideally in a CRO.
  • Experience in Oncology studies is required.
  • Excellent communication skills in written and spoken English.
  • Flexible, accountable and comfortable working in a global environment.

Responsibilities

  • Manage day-to-day operations of the project per contract and ICH/GCP guidelines.
  • 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 training.
  • Review and input for study protocol, edit check specs, data analysis plan, and final study report.

Skills

Communication skills
Oncology experience
Global/workplace flexibility
English proficiency
Accountability

Education

Bachelors in health or life sciences
Advanced degree in health or life sciences

Job description

Medpace is seeking a Clinical Trial Manager to oversee day-to-day project operations within our Singapore group. You will serve as the Sponsor contact for operational issues and ensure study deliverables meet ICH/GCP guidelines while coordinating cross-functional teams.

The role requires oncology trial experience, strong English communication, and a flexible, globally oriented mindset. This is an on-site position based in Singapore within a leading CRO environment.

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