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Clinical Project Manager

Clinical Project Manager

headcount AGZurich,Switzerland
Vor 30+ Tagen
Gehalt
110.000,00 CHF–120.000,00 CHF jährlich
Anstellungsart
  • Quick Apply
Stellenbeschreibung

Clinical Project Manager, 100%

As the main R&D work is being wrapped up, my client in Zurich is in need of a Clinical Project Manager to support outsourced studies on a global level. We are prefererring candidates who has experience with infectious diseases / vaccine development and dealing in Phase I & II studies.

Key Responsibillities :

  • Leading and managing clinical trials to ensure adherence to scope, quality, budget, timelines and performing regular risk assessments
  • Designing regulatory strategy, clinical trial design and development plans with support from the Clinical Director
  • Analyzing, interpreting and presenting clinical data internally and externally. Discussing key findings with statisticians and conducting data checks, data queries and database integrity assignments
  • Managing and preparing ethical and regulatory submissions
  • Identifying, coordinating and supporting the development of clinical assays with external partners and / or clinical sites. Keeping samples’ database and shipments tracking
  • Preparation and / or review of clinical study documentation (protocol, study plans and clinical study report)
  • Identifying, selecting, managing and overseeing external vendors, such as Contract Research Organizations (CROs), clinical sites, central laboratories etc. to ensure performance and deliverables
  • Authoring, revising and / or updating SOPs, Work Instructions and other relevant documents

You are an efficient and enthusiastic team player with :

  • Hands-on experience in successfully managing all operational aspects of clinical trials
  • Experience in the development of study-related documents like study protocols,  interim reports,  final study reports, etc
  • Experience in management of CROs, vendors and consultants
  • Good understanding of the study application packages and the communication with ECs, IRBs and regulatory authorities like EMA, FDA, etc.
  • In-depth knowledge of ICH-GCP and experience in risk assessment and development of mitigation plans