Beschreibung
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 Assistant (CTA) (m/f)
Referenz: -en
Beginn: 06/10
Dauer: 12 MM++
Ort: in Switzerland
Branche: Herstellung von pharmazeutischen Erzeugnissen
Ihre Aufgaben:
- Support the Operational Team administratively in various tasks related to study management from start-up through study completion for assigned clinical trial(s)
- Support the Operational Team administratively by drafting the minutes from the multi-disciplinary clinical trial team meetings and operational team meetings, if appropriate
- Assist with meeting preparation (e.g. schedule meetings)
- Update information in study tracking systems (e.g. CTMS)
- Set-up and maintain protocol and site level trackers (e.g. investigator list, regulatory documents, secrecy agreements, monitoring visits, etc.)
- Track and distribute study supplies (e.g. digital pens, CRFs, bulk supplies, etc.)
- Support the Operational Team by preparing and maintaining study communication tools (e.g. website, newsletter, pocket brochure, safety letters, enrollment graphs)
- Generate and distribute regulatory packages
- Assist in the coordination
- Support the Central Document Management Group and CTT by preparing the Trial Master File, and coordinating key document review
Ihre Qualifikation
- Scientific degree and/or degree in Nursing or strong administrative skills or equivalent
- Basic medical and business knowledge
- Administrative experience either in clinical research or an equally complex area
- Fluent English, verbal and written (additional languages advantageous)
- Good computer skills in current programs (i.e. MS Office, Lotus Notes) and willingness to learn new applications as required
- Good communication, interpersonal and organizational skills
- Ability to prioritize and perform multiple tasks
- Ability to work independently with strong attention to detail
- Ability to work as an effective team member within a multicultural environment
Skills:
- CRA
Keywords: CTA "Clinical Trial Administrator" Clinical Trial Assistant" Study Assistant" TMF "Trial master file" CRF