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Clinical Research Associate
Eingestellt von ITech Consult
Gesuchte Skills: Usability, Support, Design
Projektbeschreibung
CLINICAL RESEARCH ASSOCIATE
ABOUT US: ITech Consult AG is a certified ISO 9001: 2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT 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.
REFERENCE NO.: 916886NC
ROLE: Clinical Research Associate
LOCATION: Luzern Und Region, Switzerland
WORKLOAD: 100%
START DATE: From 01.01.2018
DURATION: Till 31.12.2018
PROJECT:
-Execution of external evaluations
-Support Study Manager to plan, coordinate and conduct external validation activities for new systems, software versions, and reagents. The studies are performed to confirm system design, analytical performance, usability and practicability of the new projects at independent customer sites - Organize all required activities and tasks in cooperation with other Clinical Operations departments. All studies are performed based on common SOP guidelines
-Support training activities of the evaluation sites, study monitoring, statistical calculations and interpretations, troubleshooting and study close out
-Ensure the usability of validated programs and compliance of legal and regulatory requirements at the involved evaluation sites
-Be responsible for preparation of study relevant documentation Participate in project teams
-Closely cooperate with internal and external partners to ensure optimal course of evaluation projects
REQUIREMENTS:
-Knowledge about lab automation, workflow and understanding of in vitro diagnostics laboratories
-Scientific or technical degree, preferably training as a biology/chemistry lab technician
-Good experience in Microsoft office
-Willingness to travel approximately 20%
-Driving license Cat. B
Nice to have
-Knowledge of applicable standards and regulations for clinical trial and lab conduct as well as experience in study monitoring and related tasks are a plus
-Preferable knowledge in the field of Coagulation
-Experience as CRA is a plus
LANGUAGES: English Fluent
SHOULD YOU FIND YOURSELF SUITABLE FOR THIS POSITION THEN SEND YOUR COMPLETE DOSSIER USING THIS LINK IN THE ADVERT.
*EVEN IF THIS PARTICULAR POSITION DOESN'T SUIT YOUR PROFILE WE RECOMMEND THAT YOU SEND US YOUR CV AND SHARE WITH US WHAT YOU ARE EXACTLY LOOKING FOR.
CALL US AND DISCOVER THE QUALITY OF OUR SERVICES FOR YOURSELF. WE ARE MORE THAN HAPPY TO MEET WITH YOU FOR AN INDIVIDUAL CONSULTATION. DO NOT HESITATE TO CONTACT US FOR FURTHER ENQUIRES.
OUR PAY ROLLING IS REFERRED BY 98% OF OUR FREELANCERS AS THE BEST PAY ROLLING SYSTEM IN SWITZERLAND. DO YOU REQUIRE MORE INFORMATION? FEEL FREE TO CONTACT US.
ABOUT US: ITech Consult AG is a certified ISO 9001: 2008 Swiss company with offices also located in Germany, Great Britain and Ireland. ITech Consult is specialised in delivering ICT 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.
REFERENCE NO.: 916886NC
ROLE: Clinical Research Associate
LOCATION: Luzern Und Region, Switzerland
WORKLOAD: 100%
START DATE: From 01.01.2018
DURATION: Till 31.12.2018
PROJECT:
-Execution of external evaluations
-Support Study Manager to plan, coordinate and conduct external validation activities for new systems, software versions, and reagents. The studies are performed to confirm system design, analytical performance, usability and practicability of the new projects at independent customer sites - Organize all required activities and tasks in cooperation with other Clinical Operations departments. All studies are performed based on common SOP guidelines
-Support training activities of the evaluation sites, study monitoring, statistical calculations and interpretations, troubleshooting and study close out
-Ensure the usability of validated programs and compliance of legal and regulatory requirements at the involved evaluation sites
-Be responsible for preparation of study relevant documentation Participate in project teams
-Closely cooperate with internal and external partners to ensure optimal course of evaluation projects
REQUIREMENTS:
-Knowledge about lab automation, workflow and understanding of in vitro diagnostics laboratories
-Scientific or technical degree, preferably training as a biology/chemistry lab technician
-Good experience in Microsoft office
-Willingness to travel approximately 20%
-Driving license Cat. B
Nice to have
-Knowledge of applicable standards and regulations for clinical trial and lab conduct as well as experience in study monitoring and related tasks are a plus
-Preferable knowledge in the field of Coagulation
-Experience as CRA is a plus
LANGUAGES: English Fluent
SHOULD YOU FIND YOURSELF SUITABLE FOR THIS POSITION THEN SEND YOUR COMPLETE DOSSIER USING THIS LINK IN THE ADVERT.
*EVEN IF THIS PARTICULAR POSITION DOESN'T SUIT YOUR PROFILE WE RECOMMEND THAT YOU SEND US YOUR CV AND SHARE WITH US WHAT YOU ARE EXACTLY LOOKING FOR.
CALL US AND DISCOVER THE QUALITY OF OUR SERVICES FOR YOURSELF. WE ARE MORE THAN HAPPY TO MEET WITH YOU FOR AN INDIVIDUAL CONSULTATION. DO NOT HESITATE TO CONTACT US FOR FURTHER ENQUIRES.
OUR PAY ROLLING IS REFERRED BY 98% OF OUR FREELANCERS AS THE BEST PAY ROLLING SYSTEM IN SWITZERLAND. DO YOU REQUIRE MORE INFORMATION? FEEL FREE TO CONTACT US.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Sonstiges