Praca study cra Bydgoszcz. Znaleziono 47 ofert pracy.

Manager, Study Start Up - ICF

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... preparation, review and approval of Study Master, country related and site ... preparation, review and approval of Study Master, country related and site ... and tight timelines to open study sites you should have effective ...

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Study Start Up Associate II

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... , fast-paced environment assisting the Study Start Up Team Lead in ... : • A bachelor’s degree in Paralegal Studies, Juris Doctor (law) degree , or ... environment with specific experience in study contracts review and budget negotiation ...

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CRA I

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

As a CRA, you will be joining the ... sites with all issues concerning study. Providing information to investigators about: protocol principles, study timelines, enrolment expectations and proposed ...

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Investigator Pricing Associate

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... . •Support Global Development Operations, Global Study and Clinical Management Groups and ... data to create base clinical study budget or recommendation for consultant ... and supporting documentation for clinical study or proposed compensation for consultant ...

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Senior Site Management Associate - German language skills

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... , implementing and monitoring clinical studies, with support, in a team ... training initiating and closing out study sites Conducting remote site monitoring ... management experience ideally as a CRA or an In- house CRA is required. Experience working within ...

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Clinical Trial Manager - global

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... , develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities, reviews trip ... the clinical deliverables of a study as a CTM ideally working globally • Prior CRA monitoring experience is preferred • Fluent ...

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CTA

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... with GCP and study specific requirements within target turnaround ... queries Maintain Documents and Study Files, in accordance with GCP and study specific requirements Assist with audits ... Monitoring flow of incoming study documents Follow up with homecare ...

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CRA II

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... investigative sites. Ensure compliance with study protocols, regulatory requirements, and good ...

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Senior Clinical Scientist

  • Pharmiweb
  • , Bydgoszcz,
  • 3 dni temu

... efficacy of data in ongoing studies Review tables and listings Work ... and efficacy data in ongoing studies Prior Oncology Drug Development experience ...

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