CTM Associate: Neuroscience & Ophthalmology

Medpace

Cincinnati (OH)

On-site

GBP 45,000 - 65,000

Full time

14 days+
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Benefits offered by this job

Flexible work environment
Competitive compensation and benefits
Competitive PTO packages
Structured career paths with growth
Company-sponsored employee events
Employee health and wellness

Job summary

Medpace is seeking candidates with PhDs for a full-time, office-based Associate Clinical Trial Manager to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers to perform trial management activities and transfer analytical skills into project administration.

Ideal candidates have a PhD in Life Sciences, fluent English, and the ability to thrive in a fast-paced international environment.

Qualifications

  • PhD in Life Sciences.
  • Fluency in English with solid presentation skills.
  • Ability to work in a fast-paced dynamic industry within an international team.
  • Prior experience within the CRO or pharmaceutical industry not required but will be advantageous.

Responsibilities

  • Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager
  • Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy
  • Compile and maintain project-specific status reports within the clinical trial management system
  • Interact with the internal project team, Sponsor, study sites, and third-party vendors
  • Manage and perform quality control of our internal regulatory filing system
  • Provide oversight and management of study supplies
  • Create and maintain project timelines
  • Coordinate project meetings and produce quality minutes

Skills

Fluency in English

Education

PhD in Life Sciences

Job description

Medpace is seeking candidates with PhDs for a full-time, office-based Associate Clinical Trial Manager to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers to perform trial management activities and transfer analytical skills into project administration.

Ideal candidates have a PhD in Life Sciences, fluent English, and the ability to thrive in a fast-paced international environment.

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