PhD-Ready Clinical Trial Manager (Associate)

Medpace, Inc.

Singapore

On-site

SGD 80,000 - 140,000

Full time

14 days+
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Benefits offered by this job

On-site mentors
Training programs
WFH flexibility
Social events

Job summary

Medpace seeks an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. This full-time position supports Project Coordinators and Clinical Trial Managers in project management activities and offers international exposure within a dynamic CRO environment.

Ideal candidates hold a PhD or post-doctoral experience in Life Sciences, with oncology experience, strong English communication, and solid IT skills.

Qualifications

  • PhD in Life Sciences.
  • Oncology experience.
  • Fluency in English with strong presentation skills.
  • Ability to work in a fast-paced dynamic industry within an international team.
  • Prior CRO/pharma experience not required but advantageous.
  • Excellent computer skills (Word, Excel, databases) and strong organizational/communication skills.

Responsibilities

  • Communicate and collaborate on global study activities with the project coordinator and clinical trial manager.
  • Ensure timely delivery of recurrent tasks with high accuracy.
  • Compile and maintain project status reports in the CTM system.
  • Interact with internal project team, Sponsor, study sites, and third-party vendors.
  • Provide oversight of the internal regulatory filing system.
  • Oversee study supplies management.
  • Create and maintain project timelines.
  • Coordinate project meetings and produce minutes.

Skills

Oncology experience
English fluency
Presentation skills
Fast-paced teamwork
Computer skills (Word, Excel)

Education

PhD in Life Sciences

Tools

Excel

Job description

Medpace seeks an Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Singapore. This full-time position supports Project Coordinators and Clinical Trial Managers in project management activities and offers international exposure within a dynamic CRO environment.

Ideal candidates hold a PhD or post-doctoral experience in Life Sciences, with oncology experience, strong English communication, and solid IT skills.

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