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Jobs in Prague, CZE - Covance

Study Start-up Specialist
Covance  - Prague, CZE
Clinical Research Associate
lection and preparation of essential documents - ICF development as per local legislation - Clinical trial contracts negotiation - Regulatory greenlight documents collection and compilation, CTMS, e TMF, - Cooperation with CRAs - Contact with investigative sites during site start-up activities - Working with investigative sites to collect the required investigator and regulatory documents fo ...
Clinical Research Assistants
Covance  - Prague, CZE
Clinical Research
- Assist with the management of study supplies and organize shipments - Create, update, track, and maintain study-specific ...
Clinical Research Associates
Covance  - Prague, CZE
Clinical Research Associate
he benefits of working for a company that values a WORK / LIFE BALANCE! Requirements: - Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines - Excellent understanding of Serious Adverse Event reporting - Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visi ...
Clinical Project Administrator All Levels
Covance  - Prague, CZE
Clinical Research
) - Set up and maintain clinical investigator files and documentation - Prepare study-related documents and other materials for delivery to archives, at appropriate intervals - Prepare investigator budget payments and tracking systems; generate tracking ...
Senior Manager Flexible Solutions
Covance  - Prague, CZE
Other
About the job: - Working with Clinical Operations line managers delivering the Flexible Solutions business to facilitate all aspects of operations, ensure a successful relationship, full client satisfaction and operational and service excellence. - Interact directly with client liaisons to ensure appropriate resourcing and operational excellence in service deliver ...
GSS Spec II (Study Start up Specialist II)
Covance  - Prague, CZE
Clinical Research Associate
clinical trials - Collection and preparation of essential documents - ICF development as per local legislation - Clinical trial contracts negotiation - Regulatory greenlight documents collection and compilation, CTMS, e TMF, - Cooperation with CRAs - Contact with investigative sites during site start-up activities - Working with investigative sites to collect the required investigator and r ...
 

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