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Senior Clinical Project Manager

Senior Clinical Project Manager

Informatik / Telekommunikation
  • Dauerstelle - Vollzeit
  • Referenz : INT-028850
  • Teilen:

Einzelheiten

  • Region Genf - Stadt
  • Art des Vertrags Dauerstelle - Vollzeit
  • Tätigkeitssektor Informatik / Telekommunikation

Einführung

For our client who is specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and cosmeceuticals located in Geneva, we are looking for an individual as

Senior Clinical Project Manager

(Permanent employment, fulltime). The earliest start date is as soon as possible.

Aufgabenbeschreibung

  • Implementation, execution and completion of clinical research projects sponsored according to timelines and budget.
  • Responsible of the compliance to local regulations, GCP regulations, and internal SOPs in clinical projects
  • Selection and validation of investigator/site, and vendors (ie CROs)
  • Contributing to the negotiation and preparation of contracts and budgets with third parties and sites participating in our studies
  • Responsible of developing and ensuring high quality documentation (ie from study protocol and plans to final clinical study report) throughout the clinical study.
  • Oversight and development of essential clinical documentation for regulatory and ethic committee submissions
  • Responsible for management of Contract Research Organizations (CROs) and ensure adherence to scope of work within timelines and budget
  • Management of clinical study budgets including site agreements/budget
  • Oversight of monitor performance and /or perform co-monitoring visits in sites participating to clinical projects
  • Ensure high quality data collection in clinical projects
  • Ensure that all relevant documents are properly archived in the TMF during the study
  • Participation to internal process improvements


Erforderliches Profil

  • Minimum B.Sc. degree in relevant scientific discipline e.g. Biochemistry, Microbiology, Pharmacy, Biological Sciences or Related Pharmaceutical Science
  • Minimum of 4 years of experience in clinical operations; project management skills
  • Experience in industry, especially in medical device clinical trials is a plus
  • Strong critical thinking and problem solving skills
  • Strong negotiation, communication and presentation skills across all levels
  • Able to rapidly adapt to changing environment and circumstances
  • Fluent in English and French is a strong plus


Application process:

Interested? You can find more information here: Infopackage. Please apply via the "Bewerben" button below and answer all questions, otherwise we will be unable to process your application.

Informationen

  • Agentur GPP AG - GLOBAL RECRUITMENT - +41 44 266 50 25
  • Veröffentlicht am 18. Mai 2022
  • Berater-in Marijke van Engelenburg