Clinical Trial Manager-Oncology (Immediately available)

Basel Area.
On Application
04 Sep 2018
06 Mar 2019
Contract Type


To contribute on the closure of a complex international phase I study in Oncology.

Main Responsibilities:

  • Verify subject records for completeness, subject closure, outstanding AE’s, referrals, etc.
  • Data entry or verification, query reviews, data analysis, database lock
  • Review all TMF’s and ISF’s (as applicable) documentation for completeness
  • Verify regulatory documents up to date and on file
  • Ensure completeness of final reports and submission dossier
  • Update financial records
  • Ensure unused supplies are returned or destroyed according to trial requirements

Qualifications and Experience:

  • Degree in Life Sciences
  • Experience in closing out complex international studies, ideally in phase I-II, within the pharmaceutical industry
  • Oncology experience is a must
  • Strong working knowledge of GCP, FDA regulations and current industry practices
  • Ability to work independently and deliver under limited timelines
  • Fluent in both written and spoken English
  • Relevant working/residency permit or Swiss/EU-Citizenship required

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