Clinical Research Associate (m/w/d)

Vertragsart:
Vor Ort
Start:
09/2020
Dauer:
12++
Ort:
Zug
Eingestellt:
01.08.2020
Land:
flag_no Schweiz
Projekt-ID:
1952631


Clinical Research Associate (m/w/d)- research/ life science/clinical/laboratory /English/German

Project / Role:
For our client a big pharmaceutical company in Rotkreuz we are looking for a highly motivated and qualified Clinical Research Associate (m/w/d)

Background:
Assists the conduct of clinical study activities to verify and validate new clinical software, instrument
platforms, assays and biomarkers developed by RMS. Works closely with study managers and/or other
CRA staff to complete all CRA functions associated with study planning, implementation, monitoring and
closing study conduct in accordance with the principles of Good Clinical Practice (GCP).
Tasks & Responsibilities:
* Participates in the design, planning, implementation and overall direction of clinical research projects
* Travels to field sites to monitor studies
* Works with Study Manager, Data Management and Biostatistics staff on the design of documents and processes for the collection of study data from participating sites
* Assumes responsibility for training and coordinating certification of study site personnel
* Monitors the sites and provides technical assistance, as necessary
* Manages material logistics for the studies
* Ensures site compliance with regulations and study protocol.
Must Haves:
* Apprenticeship in a laboratory area with minimum 1 year clinical research associate experience or a bachelor in a technical or life science area with minimum 1 year clinical research associate experience
* Excellent skills in basic computer applications (Word, Excel, Access, PowerPoint)
* Excellent writing and verbal communication skills in German AND English
* Basic technical understanding
* Willing to work hands on in a laboratory with infectious material

Nice to Have:
* Flexible attitude
* Experience in a hands-on work in laboratory, ideally with Polymerase Chain Reaction (PCR) methods
* Well organized and detail oriented
* Ability to work effectively in a team, and also work independently on assigned tasks
* Excellent time management skills.

Reference No.: 919581SGR
Role: Clinical Research Associate
Industry: Pharma
Location: Rotkreuz
Workload: 100%
Start:
Duration: 12 ++

Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. If the position is not a perfect match and you wish to receive other opportunities directly, you can send us your CV anyway via this advert or to jobs[at]itcag[dot]com.
Contact us for further information regarding our company, our positions or our attractive payroll-only-program:

About us:

ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed.