Globals Studies Operations Manager for international Phase II/III Trials (m/f)

Vertragsart:
Vor Ort
Start:
asap
Dauer:
12 MM++
Von:
Hays AG
Ort:
in Basel region
Eingestellt:
09.09.2010
Land:
flag_no Deutschland
Projekt-ID:
168619

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Dieses Projekt ist archiviert und leider nicht (mehr) aktiv.
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Hays ist ein weltweit führender Personaldienstleister, der sich auf die Rekrutierung von Spezialisten konzentriert - sowohl für den Projekteinsatz als auch für Festanstellungen und auf Zeit. In Deutschland, Österreich und der Schweiz vertrauen mehr als 600 internationale Topunternehmen auf unsere qualitätsgesicherten Prozesse, wenn Sie Experten suchen.


We are looking for a
Globals Studies Operations Manager for international Phase II/III Trials (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 direction and leadership to one or more clinical operations teams
  • International study coordination (1-3 studies worldwide)
  • Direct approach to country sites with local project manager
  • No direct responsibilities for CRAs
  • Develops and maintains effective working relationships with SMT members, with particular focus on affiliate teams and external CRO and co-development partner study teams
  • Develops the headquarters budget (including sample handling costs, provided by the global biosample specialist and defines the investigator budget guidelines for country sites based on assumptions from the Team Leader
  • Contributes to the development of the study timelines, resources, budget, risk, and quality plans
  • Delivers the operational elements of the study plan
  • Organizes the investigator meetings, monitor workshops, CRO kick-off meetings and leads the development and presentation of the operational aspects of the study(s). Chairs the monitor workshop meetings
  • Provides the day-to-day operational management of CROs and vendors to ensure delivery against contracted scope of work
  • Identifies areas of best practice and process improvements


Ihre Qualifikation
  • Life sciences degree with circumstantial trial management experience
  • 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
  • Good written and verbal communication skills demonstrated by an ability to present clear instruction/direction to teams at the same level in the organisation and influence at higher levels in the organisation



Skills:
- Clinical Project Management


Keywords: "Pharma Clinical Research" or " Clinical Trials" or "Clinical Operations" or " Project Management" or Study Coordination