Description
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
Clinical Trial Administrator / Clinical Trial Coordinator (m/f)
Referenz: -en
Beginn: asap
Dauer: 6 MM
Ort: in Basel region
Branche: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Provides coordination and support to Clinical Project Manager (CPM), Clinical Trial Manager (CTM) and Study Data Manager (SDM)
- Builds and maintains effective working relationships with Study Management Team (SMT) members including affiliate members
- Point of contact for defined tasks with the affiliates teams during study and supports the CPM and CTM and SDM with affiliate communication where appropriate
- Coordinates and maintains the contact details of core SMT and operations team, including country contacts and distribution lists
- Provides information to the CTM for the development of study drug supply forecasts
- Coordinates the management of all global study drug supply utilizing the designated system (ascertain packaging requirements, prepare and track drug packaging and shipment requests under the direction of the CTM)
- Liaises with affiliates and GTC (Global Trial Coordinator) to clarify local import and export requirements, retest/expiry and destruction procedures
- Manage the ordering and distribution of study-related supplies
- Ensures the timely return of site and protocol level feasibility data according to the SMT timelines and provides consolidated feedback to CTM
- Coordinates and organizes the logistics of the investigator and monitor meetings including the development and production of presentation materials under the direction of the CTM
- In collaboration with functional management, coaches and supports other Clinical Trial Administrators (CTAs)
Ihre Qualifikation
- Life sciences degree or nursing equivalent or High school graduate/educated to a secondary level plus a sound experience in clinical research/a healthcare environment
- Experience of working as part of large team with a proven ability to make an active contribution to the team's performance and team working
- Self-motivated and displays initiative (resourceful) - for instance to move actions forward without the need for continual supervision
- Able to communicate clearly and accurately in both written and spoken English
- Proven organization skills demonstrated by the ability understand instructions and deliver against commitments on time
- Has experience of using computer applications including spreadsheets, email, word-processing software
- Attention to detail
Skills:
- Clinical Project Management