International Clinical Trials Manager (m/f)

in Basel region  ‐ Onsite
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Keywords

Description



We are looking for a
International Clinical Trials Manager (m/f)

Referenz: -en
Beginn: asap
Dauer: 12 MM++
Ort: in Basel region
Branche: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen

Ihre Aufgaben:
  • Provides the operational expertise and leadership to one or more clinical operations teams in accordance with the appropriate quality standards including ICH/GCP and applicable regulations
  • Provides direction and (depending on competency level ) leadership to one or more clinical operations teams
  • Develops operational plans including site monitoring strategies, risk mitigation strategies, trial budgets, site selection, and clinical supplies management
  • Builds effective and efficient high performing operations teams and ensures team members are aware of their accountabilities, responsibilities and deliverables
  • , creates team culture and promotes team spirit
  • Develops and maintains effective working relationships with SMT members, with particular focus on affiliate teams, external providers and collaborative partners
  • Oversees the development and maintenance of study specific manuals created by the ICTA


Ihre Qualifikation
  • Proven clinical development experience of the operational aspects of all stages of clinical studies preferably working in a Global environment and/or including monitoring or leading affiliate teams, working with vendors and/or CROs, drug supply management and planning operational activities to achieve database lock
  • Experience of project managing operational aspects of a clinical study including development of timelines, budgets and resource plans
  • Proven ability to successfully achieve results within a multi-cultural and geographically diverse team
  • Experience of working as part of a large team and leading small study or functional teams, with a proven ability to be an active member of the team and motivate and lead a small team to deliver against commitments
  • Well developed written and verbal communication skills demonstrated by an ability to present clear instruction/direction to teams at the same level in the organization and influence at higher levels in the organization
  • Life sciences degree or nursing equivalent or substantial experience in a clinical research/a healthcare environment



Skills:
- Clinical trial manager


Keywords: Clinical study manager freelance contractor freelancer contract contr contracting self-employed project Projekt

Start date
ASAP
Duration
12 MM++
(extension possible)
From
Hays AG
Published at
26.07.2012
Contact person:
Jennifer Knebes
Project ID:
398094
Contract type
Freelance
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